Jobs at IQVIA

• In this key position, you’ll collaborate closely with internal teams and external partners, leading them through the planning and delivery of a supply chain that meets highest quality standards and study timelines.
• If you enjoy combining analytical thinking with operational leadership, this role offers the opportunity to make a meaningful contribution to advancing clinical research.

Your responsibilities might include:

• Interpret clinical trial protocols to create and execute an effective clinical trial supply chain solution.
• Create master English label text in accordance with relevant regulatory framework (e.g. Annex 13).
• Create and maintain demand forecasts and packaging plans so that packed clinical supplies are readily available in accordance with the project requirements.
• Initiate packaging campaigns with the assigned vendor and provide oversight to ensure on-time delivery.
• Setup, monitor, and where necessary, update study assigned Interactive Response Technology (IRT) systems to ensure study inventory is effectively managed.
• Create an appropriate distribution plan and have oversight of the assigned vendor(s) executing it.
• Ability to work independently and proactively to ensure that the supply of all trial materials is delivered to the right place at the right time.
• Provide ongoing budget tracking activities so that projects are run efficiently and in accordance with client approved quotations.
• Maintains 100% compliance on all assigned training and applies learnings to everyday practice.
• Remain up to date in all GxP and regulatory requirements applicable to the role.
• Lead client and vendor related meetings where necessary to discuss clinical supply chain topics or status updates.
• Create a Temperature Excursion management plan.
• Manage the review and assessment process of Temperature Excursions reported to the IQVIA Clinical Trial Supplies team.
• Conducts thorough and regular risk management assessments to ensure all risks are systematically reviewed and appropriate mitigations are executed.

Education, knowledge and qualifications:

• Bachelor's or higher-level degree in a science or business function.
• 2-3 Years related industry experience in Clinical Trials.
• In addition, at least 3 Years experience in Clinical Supply Chain Management.
• Ability to demonstrate good project management skills.
• Ability to create effective working relationships with internal and external stakeholders.
• Ability to demonstrate effective communication and direction.
• Ability to solve problems.
• Strong Microsoft Office skills (Word, Excel, PowerPoint, etc).
• Proficient in the English language.

go to method of application »

• Looking for data management expert, who has prior experience in performing scientific (complex) clinical data review in close collaboration with the Study Responsible Physicians (SRP) and Study Responsible Scientists (SRS)
• Prior experience of closely collaborating with the SRP, SRS, Data Management functions and the rest of the study team members when implementing the data management related activities for protocols, with focus on more complex indication and therapy related elements of the study.
• Has prior experience of being involved and driving discussions with SRP/SRS and collaborates with the Data management team to establish, align, and confirm scientific clinical data review expectations for assigned trial(s).
• Extensive prior experience of 5+ years supporting studies within the therapeutic area Oncology or CV&M.

Rave experience mandatory

Deliverables:

• Services rendered will adhere to applicable Client SOPs, WIs, policies, local regulatory requirements, ICH-GCP, etc.
• Provides scientific data review support for more than one low to moderate complexity trial or one high complexity trial.
• The data management expert who, within the therapeutic area, is performing scientific (complex) clinical data review in close collaboration with the Study Responsible Physicians (SRP) and Study Responsible Scientists (SRS). Tapping into technical and clinical expertise, closely collaborating with the SRP, SRS, Data Management functions and the rest of the study team members when implementing the data management related activities for protocols, with focus on more complex indication and therapy related elements of the study. Reviews all necessary data flows, the Data Management Plans and performs continuous (complex) data review activities on the studies in the assigned program.
• Involved in study related activities from the protocol design stage onwards, providing input into the study specific and/or indication specific data collection tools.
• Reviews (complex) scientific study data, manages CDM and SRS/SRP related queries in EDC system. Involvement in other review activities (e.g., Coding, SAE reconciliation) is possible.
• Leads and/or attends meetings as appropriate.
• Takes a leadership role with SRP/SRS and collaborates with the GDM to establish, align and confirm scientific clinical data review expectations for assigned trial(s).

With the trial customer, CRO and other functional partners in relation to CDM related activities:

• Reviews content and integration requirements for eCRF and other data collection tools
• Establishes conventions and quality expectations for clinical data.
• Set timelines and follow‐up regularly to ensure delivery of all Clinical Data Management milestones
• Creates the Integrated Review Plan ensuring appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency. Reviews related clinical data management documents. Ensures compliance with regulatory guidelines and documentation requirements.
• Ensures real‐time inspection readiness of all assigned deliverables for the trial; participate in Regulatory Agency inspection and Client internal audits as necessary.
• Plans and tracks applicable CDM deliverables. Ensures CDM deliverables are on time.
• Takes a leadership role in collaborating with the SRS/SRP to ensure that DM and Therapeutic Area trial needs and deliverables are met.
• Identifies and communicates lessons learned, best practices and frequently asked questions at the trial level.
• Identifies and participates in process, system, and tool improvement initiatives within clinical data management.
• Therapeutic Area - Oncology, Cardiovascular and Immunology

Education/Experience

• BS/BA degree or higher preferably in Health Sciences, or BS/BA degree or higher with professional clinical experience/exposure.
• 5 years Data Management experience performing scientific (complex) clinical data review
• Knowledge in medical terminology would be preferable
• Must have experience in supporting the eCRF build
• Rave knowledge and experience mandatory

go to method of application »

• Looking for data management expert, who has prior experience in performing scientific (complex) clinical data review in close collaboration with the Study Responsible Physicians (SRP) and Study Responsible Scientists (SRS)
• Prior experience of closely collaborating with the SRP, SRS, Data Management functions and the rest of the study team members when implementing the data management related activities for protocols, with focus on more complex indication and therapy related elements of the study.
• Has prior experience of being involved and driving discussions with SRP/SRS and collaborates with the Data management team to establish, align, and confirm scientific clinical data review expectations for assigned trial(s).
• Extensive prior experience of 5+ years supporting studies within the therapeutic area Oncology or CV&M.

Rave experience mandatory

Deliverables:

• Services rendered will adhere to applicable Client SOPs, WIs, policies, local regulatory requirements, ICH-GCP, etc.
• Provides scientific data review support for more than one low to moderate complexity trial or one high complexity trial.
• The data management expert who, within the therapeutic area, is performing scientific (complex) clinical data review in close collaboration with the Study Responsible Physicians (SRP) and Study Responsible Scientists (SRS). Tapping into technical and clinical expertise, closely collaborating with the SRP, SRS, Data Management functions and the rest of the study team members when implementing the data management related activities for protocols, with focus on more complex indication and therapy related elements of the study. Reviews all necessary data flows, the Data Management Plans and performs continuous (complex) data review activities on the studies in the assigned program.
• Involved in study related activities from the protocol design stage onwards, providing input into the study specific and/or indication specific data collection tools.
• Reviews (complex) scientific study data, manages CDM and SRS/SRP related queries in EDC system. Involvement in other review activities (e.g., Coding, SAE reconciliation) is possible.
• Leads and/or attends meetings as appropriate.
• Takes a leadership role with SRP/SRS and collaborates with the GDM to establish, align and confirm scientific clinical data review expectations for assigned trial(s).

With the trial customer, CRO and other functional partners in relation to CDM related activities:

• Reviews content and integration requirements for eCRF and other data collection tools
• Establishes conventions and quality expectations for clinical data.
• Set timelines and follow‐up regularly to ensure delivery of all Clinical Data Management milestones
• Creates the Integrated Review Plan ensuring appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency. Reviews related clinical data management documents. Ensures compliance with regulatory guidelines and documentation requirements.
• Ensures real‐time inspection readiness of all assigned deliverables for the trial; participate in Regulatory Agency inspection and Client internal audits as necessary.
• Plans and tracks applicable CDM deliverables. Ensures CDM deliverables are on time.
• Takes a leadership role in collaborating with the SRS/SRP to ensure that DM and Therapeutic Area trial needs and deliverables are met.
• Identifies and communicates lessons learned, best practices and frequently asked questions at the trial level.
• Identifies and participates in process, system, and tool improvement initiatives within clinical data management.
• Therapeutic Area - Oncology, Cardiovascular and Immunology

Education/Experience

• BS/BA degree or higher preferably in Health Sciences, or BS/BA degree or higher with professional clinical experience/exposure.
• 5 years Data Management experience performing scientific (complex) clinical data review
• Knowledge in medical terminology would be preferable
• Must have experience in supporting the eCRF build
• Rave knowledge and experience mandatory

go to method of application »

• Looking for data management expert, who has prior experience in performing scientific (complex) clinical data review in close collaboration with the Study Responsible Physicians (SRP) and Study Responsible Scientists (SRS)
• Prior experience of closely collaborating with the SRP, SRS, Data Management functions and the rest of the study team members when implementing the data management related activities for protocols, with focus on more complex indication and therapy related elements of the study.
• Has prior experience of being involved and driving discussions with SRP/SRS and collaborates with the Data management team to establish, align, and confirm scientific clinical data review expectations for assigned trial(s).
• Extensive prior experience of 5+ years supporting studies within the therapeutic area Oncology or CV&M.

Rave experience mandatory

Deliverables:

• Services rendered will adhere to applicable Client SOPs, WIs, policies, local regulatory requirements, ICH-GCP, etc.
• Provides scientific data review support for more than one low to moderate complexity trial or one high complexity trial.
• The data management expert who, within the therapeutic area, is performing scientific (complex) clinical data review in close collaboration with the Study Responsible Physicians (SRP) and Study Responsible Scientists (SRS). Tapping into technical and clinical expertise, closely collaborating with the SRP, SRS, Data Management functions and the rest of the study team members when implementing the data management related activities for protocols, with focus on more complex indication and therapy related elements of the study. Reviews all necessary data flows, the Data Management Plans and performs continuous (complex) data review activities on the studies in the assigned program.
• Involved in study related activities from the protocol design stage onwards, providing input into the study specific and/or indication specific data collection tools.
• Reviews (complex) scientific study data, manages CDM and SRS/SRP related queries in EDC system. Involvement in other review activities (e.g., Coding, SAE reconciliation) is possible.
• Leads and/or attends meetings as appropriate.
• Takes a leadership role with SRP/SRS and collaborates with the GDM to establish, align and confirm scientific clinical data review expectations for assigned trial(s).

With the trial customer, CRO and other functional partners in relation to CDM related activities:

• Reviews content and integration requirements for eCRF and other data collection tools
• Establishes conventions and quality expectations for clinical data.
• Set timelines and follow‐up regularly to ensure delivery of all Clinical Data Management milestones
• Creates the Integrated Review Plan ensuring appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency. Reviews related clinical data management documents. Ensures compliance with regulatory guidelines and documentation requirements.
• Ensures real‐time inspection readiness of all assigned deliverables for the trial; participate in Regulatory Agency inspection and Client internal audits as necessary.
• Plans and tracks applicable CDM deliverables. Ensures CDM deliverables are on time.
• Takes a leadership role in collaborating with the SRS/SRP to ensure that DM and Therapeutic Area trial needs and deliverables are met.
• Identifies and communicates lessons learned, best practices and frequently asked questions at the trial level.
• Identifies and participates in process, system, and tool improvement initiatives within clinical data management.
• Therapeutic Area - Oncology, Cardiovascular and Immunology

Education/Experience

• BS/BA degree or higher preferably in Health Sciences, or BS/BA degree or higher with professional clinical experience/exposure.
• 5 years Data Management experience performing scientific (complex) clinical data review
• Knowledge in medical terminology would be preferable
• Must have experience in supporting the eCRF build
• Rave knowledge and experience mandatory

go to method of application »

• Provides data management support, oversight and/or accountability for one or more clinical trials.
• Take the lead with the trial customer(s) and other internal and external partners to establish, align and confirm data management expectations
• Creating, planning, and tracking content, format, quality, and timing of data management deliverables, including, but not limited to, CRF, data review plan, QC plan, oversight plan, database release plan, final datasets, submission plan and archival.
• With the trial customer and other functional partners: – Gathers content and integration requirements for eCRF and other data collection tools.
• Establishes conventions and quality expectations for clinical data.
• Establishes expectations for dataset content and structure.
• Set timelines and follow-up to ensure delivery of all Data Management milestones.
• Performs trial level oversight controls, as appropriate, as described in the oversight plan, QC process and work instructions with minimal DML direction.
• Creates clinical data management documents (including submission package) ensuring appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency. Ensures compliance with regulatory guidelines and the documentation matrix.
• Ensures real-time inspection readiness of all Data Management deliverables for the trial; Participate in Regulatory Agency and audits, as necessary.
• Helps plan, create and track content, format, quality, and timing of data
• management deliverables, including, but not limited to, Case Report Form, data review plan, QC plan, oversight plan, database release plan, final datasets, submission plan and archival.
• Ensures deliverables are on time.
• Participates in the assigned clinical working group(s) to ensure that Data
• Management and Therapeutic Area trial needs and deliverables are met.
• Helps Identify and communicate lessons learned, best practices and frequently asked questions at the trial level.
• Presents and trains at investigator and monitor meetings

Education/Experience

• BS/BA degree or higher preferably in Health Sciences, or BS/BA degree or higher with professional clinical experience/exposure.
• 5 years Data management experience.
• 3 years lead/co-lead experience
• Vendor Management experience
• RAVE experience

go to method of application »

• Provides data management support, oversight and/or accountability for one or more clinical trials.
• Take the lead with the trial customer(s) and other internal and external partners to establish, align and confirm data management expectations
• Creating, planning, and tracking content, format, quality, and timing of data management deliverables, including, but not limited to, CRF, data review plan, QC plan, oversight plan, database release plan, final datasets, submission plan and archival.
• With the trial customer and other functional partners: – Gathers content and integration requirements for eCRF and other data collection tools.
• Establishes conventions and quality expectations for clinical data.
• Establishes expectations for dataset content and structure.
• Set timelines and follow-up to ensure delivery of all Data Management milestones.
• Performs trial level oversight controls, as appropriate, as described in the oversight plan, QC process and work instructions with minimal DML direction.
• Creates clinical data management documents (including submission package) ensuring appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency. Ensures compliance with regulatory guidelines and the documentation matrix.
• Ensures real-time inspection readiness of all Data Management deliverables for the trial; Participate in Regulatory Agency and audits, as necessary.
• Helps plan, create and track content, format, quality, and timing of data
• management deliverables, including, but not limited to, Case Report Form, data review plan, QC plan, oversight plan, database release plan, final datasets, submission plan and archival.
• Ensures deliverables are on time.
• Participates in the assigned clinical working group(s) to ensure that Data
• Management and Therapeutic Area trial needs and deliverables are met.
• Helps Identify and communicate lessons learned, best practices and frequently asked questions at the trial level.
• Presents and trains at investigator and monitor meetings

Education/Experience

• BS/BA degree or higher preferably in Health Sciences, or BS/BA degree or higher with professional clinical experience/exposure.
• 5 years Data management experience.
• 3 years lead/co-lead experience
• Vendor Management experience
• RAVE experience

go to method of application »

• Provides data management support, oversight and/or accountability for one or more clinical trials.
• Take the lead with the trial customer(s) and other internal and external partners to establish, align and confirm data management expectations
• Creating, planning, and tracking content, format, quality, and timing of data management deliverables, including, but not limited to, CRF, data review plan, QC plan, oversight plan, database release plan, final datasets, submission plan and archival.
• With the trial customer and other functional partners: – Gathers content and integration requirements for eCRF and other data collection tools.
• Establishes conventions and quality expectations for clinical data.
• Establishes expectations for dataset content and structure.
• Set timelines and follow-up to ensure delivery of all Data Management milestones.
• Performs trial level oversight controls, as appropriate, as described in the oversight plan, QC process and work instructions with minimal DML direction.
• Creates clinical data management documents (including submission package) ensuring appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency. Ensures compliance with regulatory guidelines and the documentation matrix.
• Ensures real-time inspection readiness of all Data Management deliverables for the trial; Participate in Regulatory Agency and audits, as necessary.
• Helps plan, create and track content, format, quality, and timing of data
• management deliverables, including, but not limited to, Case Report Form, data review plan, QC plan, oversight plan, database release plan, final datasets, submission plan and archival.
• Ensures deliverables are on time.
• Participates in the assigned clinical working group(s) to ensure that Data
• Management and Therapeutic Area trial needs and deliverables are met.
• Helps Identify and communicate lessons learned, best practices and frequently asked questions at the trial level.
• Presents and trains at investigator and monitor meetings

Education/Experience

• BS/BA degree or higher preferably in Health Sciences, or BS/BA degree or higher with professional clinical experience/exposure.
• 5 years Data management experience.
• 3 years lead/co-lead experience
• Vendor Management experience
• RAVE experience

go to method of application »

About the Role

As a Sr CEVA Specialist, you will manage and deliver comprehensive Clinical Event Validation and Adjudication (CEVA) services, supporting committees such as:

• Endpoint Adjudication Committees
• Core Laboratories
• Image Review Committees
• Data Monitoring Committees
• Safety Monitoring Committees
• Steering Committees / Advisory Boards
• You’ll serve as a trusted customer partner—guiding projects from scoping and proposals through delivery, ensuring clarity, transparency, and exceptional service every step of the way.

What You’ll Do

• Lead and coordinate adjudication and oversight committees across CEVA service lines
• Serve as the primary customer interface, ensuring strong communication and timely deliverables
• Develop project-specific documentation, reports, listings, and training
• Collaborate with internal/external teams to develop and optimize electronic systems
• Manage project profitability, revenue forecasting, and financial performance
• Mentor developing specialists within the CEVA team
• Identify risks and implement innovative process improvements using Lean methodologies
• Support proposal development, bid defenses, and sales presentations
• Participate in audits, inspections, and high-level customer meetings
• Manage multiple, complex projects with competing priorities
• Drive customer loyalty through exceptional service delivery

Qualifications & Experience

• Bachelor’s degree in Life Sciences, Health Sciences, or equivalent
• 5+ years of clinical research experience
• Prior customer-facing experience is essential
• Solid knowledge of GCP, ICH guidelines, and relevant regulatory standards
• Strong project management capability and ability to lead teleconferences and meetings
• Excellent communication, organizational, prioritization, and problem‑solving skills
• Ability to manage ambiguity and work independently across multiple projects
• Skilled in conflict resolution, influencing others, and strategic thinking
• Cross‑trained in at least two CEVA service lines (preferred)
• Financial awareness, including budgeting and revenue management (or willingness to develop)

go to method of application »

About the Role

As a Sr CEVA Specialist, you will manage and deliver comprehensive Clinical Event Validation and Adjudication (CEVA) services, supporting committees such as:

• Endpoint Adjudication Committees
• Core Laboratories
• Image Review Committees
• Data Monitoring Committees
• Safety Monitoring Committees
• Steering Committees / Advisory Boards
• You’ll serve as a trusted customer partner—guiding projects from scoping and proposals through delivery, ensuring clarity, transparency, and exceptional service every step of the way.

What You’ll Do

• Lead and coordinate adjudication and oversight committees across CEVA service lines
• Serve as the primary customer interface, ensuring strong communication and timely deliverables
• Develop project-specific documentation, reports, listings, and training
• Collaborate with internal/external teams to develop and optimize electronic systems
• Manage project profitability, revenue forecasting, and financial performance
• Mentor developing specialists within the CEVA team
• Identify risks and implement innovative process improvements using Lean methodologies
• Support proposal development, bid defenses, and sales presentations
• Participate in audits, inspections, and high-level customer meetings
• Manage multiple, complex projects with competing priorities
• Drive customer loyalty through exceptional service delivery

Qualifications & Experience

• Bachelor’s degree in Life Sciences, Health Sciences, or equivalent
• 5+ years of clinical research experience
• Prior customer-facing experience is essential
• Solid knowledge of GCP, ICH guidelines, and relevant regulatory standards
• Strong project management capability and ability to lead teleconferences and meetings
• Excellent communication, organizational, prioritization, and problem‑solving skills
• Ability to manage ambiguity and work independently across multiple projects
• Skilled in conflict resolution, influencing others, and strategic thinking
• Cross‑trained in at least two CEVA service lines (preferred)
• Financial awareness, including budgeting and revenue management (or willingness to develop)

go to method of application »

Job Overview

• Manage end-to-end delivery of data management services for single/multi-service projects with minimal guidance, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Data Management (DM) team to provide high quality data management products that meet customer needs. Provide leadership to the team in the areas of project planning, execution, and close-out; Overview of financial management for data management activities; communications; and milestone deliverables. Perform role of Data Team Lead (DTL).

Essential Functions

• Gather Study Set up requirements through discussion and communication with relevant stakeholders.
• With Minimal guidance - support, overview of validation of new Device integrations.
• Oversight & Perform regular Data cleaning activities to ensure clean data with quality and timely deliverables to sponsor.
• Ensure that all the deliverables are of expected quality standards and meet customer expectations.
• With guidance, ensure service and quality meet agreed upon timelines and deliverables in contract/Scope of Work (SOW).
• Support Training of New joiners.
• Lead internal study meetings and internal/ sponsor audits and participate in Study Kick off meetings and other sponsor meetings.
• Tracks and manages the projects, oversee project progress, identify risks and take corrective action to rectify any errors as recommended as required.
• With Guidance manage & oversight the implementation of new technology / database revisions.
• Work closely with the programming team for process innovation and automation.
• Be compliant to trainings and eSOP reading.
• Provide review and expert opinion in developing, revising, and maintaining core operating procedures and working instructions.
• Communication with Line Manager, and other team members across functions should be collaborative.
• Perform other duties as directed by Line Manager.

Qualifications

• Bachelor's degree in health, clinical, biological or mathematical sciences, or related field with proven experience in Data Management Req
• 3 -4 years direct Data Management experience, including a minimum of 1 year as a CDM project lead. Pref
• English Fluency Spoken and English Advanced
• Advanced computer applications like Microsoft excel, word, Inbox etc Advanced
• Should have Advanced understanding of Drug development lifecycle and Overall Clinical research process Advanced

go to method of application »

Job Overview

• Manage end-to-end delivery of data management services for single/multi-service projects with minimal guidance, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Data Management (DM) team to provide high quality data management products that meet customer needs. Provide leadership to the team in the areas of project planning, execution, and close-out; Overview of financial management for data management activities; communications; and milestone deliverables. Perform role of Data Team Lead (DTL).

Essential Functions

• Gather Study Set up requirements through discussion and communication with relevant stakeholders.
• With Minimal guidance - support, overview of validation of new Device integrations.
• Oversight & Perform regular Data cleaning activities to ensure clean data with quality and timely deliverables to sponsor.
• Ensure that all the deliverables are of expected quality standards and meet customer expectations.
• With guidance, ensure service and quality meet agreed upon timelines and deliverables in contract/Scope of Work (SOW).
• Support Training of New joiners.
• Lead internal study meetings and internal/ sponsor audits and participate in Study Kick off meetings and other sponsor meetings.
• Tracks and manages the projects, oversee project progress, identify risks and take corrective action to rectify any errors as recommended as required.
• With Guidance manage & oversight the implementation of new technology / database revisions.
• Work closely with the programming team for process innovation and automation.
• Be compliant to trainings and eSOP reading.
• Provide review and expert opinion in developing, revising, and maintaining core operating procedures and working instructions.
• Communication with Line Manager, and other team members across functions should be collaborative.
• Perform other duties as directed by Line Manager.

Qualifications

• Bachelor's degree in health, clinical, biological or mathematical sciences, or related field with proven experience in Data Management Req
• 3 -4 years direct Data Management experience, including a minimum of 1 year as a CDM project lead. Pref
• English Fluency Spoken and English Advanced
• Advanced computer applications like Microsoft excel, word, Inbox etc Advanced
• Should have Advanced understanding of Drug development lifecycle and Overall Clinical research process Advanced

go to method of application »

Job Overview

• Manage end-to-end delivery of data management services for single/multi-service projects with minimal guidance, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Data Management (DM) team to provide high quality data management products that meet customer needs. Provide leadership to the team in the areas of project planning, execution, and close-out; Overview of financial management for data management activities; communications; and milestone deliverables. Perform role of Data Team Lead (DTL).

Essential Functions

• Gather Study Set up requirements through discussion and communication with relevant stakeholders.
• With Minimal guidance - support, overview of validation of new Device integrations.
• Oversight & Perform regular Data cleaning activities to ensure clean data with quality and timely deliverables to sponsor.
• Ensure that all the deliverables are of expected quality standards and meet customer expectations.
• With guidance, ensure service and quality meet agreed upon timelines and deliverables in contract/Scope of Work (SOW).
• Support Training of New joiners.
• Lead internal study meetings and internal/ sponsor audits and participate in Study Kick off meetings and other sponsor meetings.
• Tracks and manages the projects, oversee project progress, identify risks and take corrective action to rectify any errors as recommended as required.
• With Guidance manage & oversight the implementation of new technology / database revisions.
• Work closely with the programming team for process innovation and automation.
• Be compliant to trainings and eSOP reading.
• Provide review and expert opinion in developing, revising, and maintaining core operating procedures and working instructions.
• Communication with Line Manager, and other team members across functions should be collaborative.
• Perform other duties as directed by Line Manager.

Qualifications

• Bachelor's degree in health, clinical, biological or mathematical sciences, or related field with proven experience in Data Management Req
• 3 -4 years direct Data Management experience, including a minimum of 1 year as a CDM project lead. Pref
• English Fluency Spoken and English Advanced
• Advanced computer applications like Microsoft excel, word, Inbox etc Advanced
• Should have Advanced understanding of Drug development lifecycle and Overall Clinical research process Advanced

go to method of application »

Advance level role

• Provide timely status updates including issues & risks to DM and DMLs as needed
• Act as the Point of contact for Clinical Data Manager, working pro-actively to identify risks and provide mitigations
• May communicate with the vendors to resolve reconciliation issues.
• Provide input to Study set up activities including but not limited to creation of DVRs
• Create and/or provide inputs to Data Management documents (e.g. eCRF completion guidelines, etc.).
• Review and provide inputs to Data Management documents (e.g. IRP, DMP, etc.)
• Assign work to allocated CDAs on a trial. Coordinate work of CDAs assigned to a study working closely with the Global Data Manager to understand priorities and timelines.
• Assist the Data Management Leader in TMF compliance reviews.
• Train and mentor CDA staff
• May serve as an SME and participate in SME forums
• May act as delegate for Data Manager, as needed

Education and Experience Guidelines:

• Bachelor’s degree in a Health or Science discipline with experience in clinical research.
• Experience CDA ADVANCED level: >3 year of experience Data Management experience
• Data Management experience and experience working on a clinical trial mandatory.
• Rave experience mandatory
• Experience working in highly diverse teams within clinical research; cross-functional, global, multi- regional.
• Knowledge of current industry standards (e.g., CDISC, SDTM, CDASH, etc.) for Advanced CDA.
• Knowledge of technology platforms and systems to capture and process data
• Project management skills.
• Vendor management skills.
• Proficiency with Microsoft Office tools

go to method of application »

Advance level role

• Provide timely status updates including issues & risks to DM and DMLs as needed
• Act as the Point of contact for Clinical Data Manager, working pro-actively to identify risks and provide mitigations
• May communicate with the vendors to resolve reconciliation issues.
• Provide input to Study set up activities including but not limited to creation of DVRs
• Create and/or provide inputs to Data Management documents (e.g. eCRF completion guidelines, etc.).
• Review and provide inputs to Data Management documents (e.g. IRP, DMP, etc.)
• Assign work to allocated CDAs on a trial. Coordinate work of CDAs assigned to a study working closely with the Global Data Manager to understand priorities and timelines.
• Assist the Data Management Leader in TMF compliance reviews.
• Train and mentor CDA staff
• May serve as an SME and participate in SME forums
• May act as delegate for Data Manager, as needed

Education and Experience Guidelines:

• Bachelor’s degree in a Health or Science discipline with experience in clinical research.
• Experience CDA ADVANCED level: >3 year of experience Data Management experience
• Data Management experience and experience working on a clinical trial mandatory.
• Rave experience mandatory
• Experience working in highly diverse teams within clinical research; cross-functional, global, multi- regional.
• Knowledge of current industry standards (e.g., CDISC, SDTM, CDASH, etc.) for Advanced CDA.
• Knowledge of technology platforms and systems to capture and process data
• Project management skills.
• Vendor management skills.
• Proficiency with Microsoft Office tools

go to method of application »

Advance level role

• Provide timely status updates including issues & risks to DM and DMLs as needed
• Act as the Point of contact for Clinical Data Manager, working pro-actively to identify risks and provide mitigations
• May communicate with the vendors to resolve reconciliation issues.
• Provide input to Study set up activities including but not limited to creation of DVRs
• Create and/or provide inputs to Data Management documents (e.g. eCRF completion guidelines, etc.).
• Review and provide inputs to Data Management documents (e.g. IRP, DMP, etc.)
• Assign work to allocated CDAs on a trial. Coordinate work of CDAs assigned to a study working closely with the Global Data Manager to understand priorities and timelines.
• Assist the Data Management Leader in TMF compliance reviews.
• Train and mentor CDA staff
• May serve as an SME and participate in SME forums
• May act as delegate for Data Manager, as needed

Education and Experience Guidelines:

• Bachelor’s degree in a Health or Science discipline with experience in clinical research.
• Experience CDA ADVANCED level: >3 year of experience Data Management experience
• Data Management experience and experience working on a clinical trial mandatory.
• Rave experience mandatory
• Experience working in highly diverse teams within clinical research; cross-functional, global, multi- regional.
• Knowledge of current industry standards (e.g., CDISC, SDTM, CDASH, etc.) for Advanced CDA.
• Knowledge of technology platforms and systems to capture and process data
• Project management skills.
• Vendor management skills.
• Proficiency with Microsoft Office tools

go to method of application »

About the Role

• IQVIA is seeking a highly organized and detail‑oriented Administrator to provide comprehensive administrative support to an IQVIA‑managed project. This role is essential to ensuring smooth daily operations, supporting internal teams, maintaining accurate documentation, and enabling efficient service delivery across the project.
• The ideal candidate is proactive, professional, and capable of managing multiple responsibilities with accuracy and confidentiality and French Speaking.

Key Responsibilities

General Administrative Support

• Manage and respond to emails professionally and promptly.
• Maintain efficient and organized filing systems.
• Ensure accurate and up‑to‑date record‑keeping.

Data Entry & Management

• Update and maintain databases and spreadsheets.
• Ensure data accuracy, consistency, and integrity across all systems.

Communication & Coordination

• Liaise effectively with internal teams and external stakeholders.
• Coordinate meetings, follow‑ups, and general communication workflows.

Reporting

• Compile and prepare monthly reports and activity summaries.
• Support data analysis and assist with presenting findings.

Compliance & Documentation

• Ensure all documentation meets compliance and policy standards.
• Maintain strict confidentiality and adhere to data protection regulations.

Expense Management

• Manage Concur and cash claim submissions.
• Ensure accuracy and alignment with expense policies.

Leave Management

• Monitor and track employee leave balances.
• Communicate leave status updates to employees and managers.

Travel & IT Support

• Coordinate travel arrangements including flights, accommodation, and logistics for project contractors.
• Support IT‑related administrative requests as required.

Vendor Management

• Review and submit vendor invoices for payment.
• Prevent errors and duplication; ensure policy alignment.
• Verify availability of required supporting documentation.

Other Duties as Required

• Support ad hoc tasks as directed by the project team.
• Manage invoicing processes.
• Follow up on equipment requests and deliveries.
• Maintain and update SOPs.
• Ensure contract alignment and support country‑specific processes where applicable.

Qualifications & Skills

• Proven experience in administrative or coordination roles.
• Language Requirement French
• Strong organizational and time‑management skills.
• Excellent written and verbal communication abilities.
• Proficient in MS Office and database systems.
• High attention to detail and ability to manage multiple priorities.
• Ability to maintain confidentiality and handle sensitive information responsibly.

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About the Role

• IQVIA is recruiting a skilled and motivated Professional Sales Representative to support a specialized Dental Portfolio across the Gauteng region. This field-based position focuses on scientific selling, building long-term professional relationships, and driving sales performance through dentists and dental-focused pharmacies.
• You will engage with dental professionals, oral health educators, specialized pharmacies, and dental teaching institutions to ensure strong brand advocacy, customer education, and territory growth. This is a high-impact commercial role with excellent development opportunities within IQVIA’s expanding ecosystem.

Target Customer Base (Mandatory Focus)

The successful candidate will engage with:

• General Practice Dentists
• Dental Hygienists & Oral Health Practitioners
• Dental Specialists (e.g., Orthodontists, Periodontists – where relevant)
• Pharmacies specializing in dental products, patient training, and oral care category management
• Dental schools, educators, and teaching institutions

Prior experience calling on dentists and/or dental-focused pharmacies is essential.

Role Scope & Development Focus

Key Experiences

• Previous experience detailing to dentists (mandatory)
• Pharmaceutical, oral care, or medical device sales experience advantageous
• Proven ability to independently manage a field sales territory
• Strong relationship-building skills with healthcare professionals

Development Focus

• Deepen dental and oral-care product knowledge
• Strengthen scientific detailing and influencing capabilities
• Enhance data-driven planning, CRM utilization, and market analysis skills
• Grow within IQVIA’s commercial organization, with strong potential for contract renewal

Key Responsibilities

Territory Management & Field Execution

• Conduct 8–12 targeted sales calls per day, primarily to dentists and specialist dental pharmacies
• Deliver professional product detailing, clinical discussions, and educational engagement
• Facilitate practice-based training, lunch-and-learns, and product demonstrations
• Ensure 95–100% territory coverage across all dental and pharmacy accounts
• Manage territory activities within approved expense budgets
• Record calls, insights, and follow-ups using Salesforce/iQCRM
• Provide excellent customer support, including order management and product follow-up
• Represent IQVIA and client brands at dental congresses, CPD events, and industry conventions

Professional & Scientific Engagement

• Build strong partnerships with dental associations, dental school faculty, and oral health groups
• Support and deliver CPD/CME-aligned scientific education sessions
• Host webinars, group training, and educational sessions for dental professionals
• Identify and support collaboration with key opinion leaders in dentistry

Business & Organizational Development

• Develop and execute a clear territory action plan aligned to brand objectives
• Review sales data, CRM insights, and competitive dynamics to refine strategy
• Deliver quarterly business reviews with field insights and opportunities
• Participate in strategic initiatives, representing on-the-ground commercial realities

Personal & Professional Development

• Complete all IQVIA and client training, certification, and compliance modules
• Maintain strong product knowledge and commercial excellence in dental science
• Demonstrate accountability, discipline, and consistent delivery against KPIs
• Uphold IQVIA’s ethical engagement and compliance standards

Minimum Qualifications & Requirements

• Matric essential; healthcare, dental, or commercial diploma/degree advantageous
• Experience calling on dentists is mandatory
• Experience calling on pharmacies (especially dental-focused) advantageous
• Must reside in Gauteng and travel daily within the territory
• Valid driver’s license and reliable transport
• Strong communication, influencing, and organizational skills
• Ability to work independently in a remote, field-based environment

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About the Role

• IQVIA is seeking a dynamic and purpose-driven Sales Lead to champion a specialized Dental Portfolio across the Gauteng region. This is a leadership-focused, field-based position ideal for a commercially minded professional who thrives on influencing dental practitioners, driving scientific engagement, and leading field execution with excellence.
• The Sales Lead will represent IQVIA and its client across the dental landscape, building strong professional relationships, executing strategic territory plans, and driving growth through education, advocacy, and persistent customer engagement.
• This role also includes leadership responsibility for 1–2 Professional Sales Representatives within the territory.

Target Customer Base

You will engage with a broad variety of dental professionals and stakeholders, including:

• Dentists (primary and mandatory focus)
• Dental hygienists and oral health practitioners
• Dental specialists (e.g., periodontists, orthodontists)
• Pharmacies specializing in dental/ oral-care products and category management
• Dental schools, lecturers, and training institutions

Experience engaging dentists with established relationships is essential.

Minimum Qualifications & Experience

Essential

• Tertiary qualification required
  • Preferred: Dental, Oral Health, Dental Technology, or related clinical science qualification
• Strong leadership capabilities
• Valid driver’s license
• Must reside in Gauteng

Preferred

• Experience in pharmaceutical, dental, or healthcare product sales
• Previous leadership, coaching, or sales management exposure
• Experience in dental professional environments
• Salesforce CRM proficiency (or similar CRM system)
• Comfortable working independently as part of a remote, field-based team

Key Responsibilities

Territory Leadership & Field Execution

• Lead all field-based activities across Gauteng with full ownership and accountability
• Conduct 8–12 high-quality daily sales calls to dentists and dental-focused pharmacies
• Deliver professional detailing, scientific discussions, and value-driven engagement
• Facilitate product training sessions, in-practice workshops, and clinical demonstrations
• Achieve 95–100% coverage of all allocated dental and pharmacy accounts
• Manage and report on territory budgets
• Capture all interactions and insights on Salesforce CRM
• Provide exceptional customer service and follow-through

Scientific & Professional Engagement

• Engage dental associations, educators, and training bodies
• Deliver scientific education: CPD sessions, webinars, workshops, and small-group training
• Build relationships with key opinion leaders in dentistry and specialized pharmacy groups
• Ensure all communication meets scientific accuracy and compliance standards

Business Planning & Organizational Contribution

• Develop robust business plans based on analytics, insights, and brand strategy
• Analyze monthly sales data and CRM insights to adjust territory strategy
• Present quarterly business reviews
• Participate in strategic projects and cross-functional collaboration
• Engage actively in internal meetings, training, and client-facing interactions

Leadership & Development

• Demonstrate strong leadership that drives performance, client confidence, and collaboration
• Mentor or support junior representatives to foster a high-performance culture
• Participate in IQVIA development programmes with a path to future leadership roles
• Maintain up-to-date knowledge on product, therapeutic areas, and selling skills