Jobs at IQVIA

Role Overview:

• This unique role within IQVIA lends itself to a technically minded person with strong communication skills and SDTM knowledge. Having experience with SAS programming will be key for this position. The role can be based remotely from anywhere in Europe or in South Africa.
• This role is part of a sponsor dedicated project where you will be working with the client directly to manage Database SDTM Deliveries.
• The primary functions of this role will be to define SDTM specification and Programming including SDTM review ensuring quality and completeness of SDTM format data.

Primary Functions:

• Review and programming of SDTM deliveries
• Build and review SDTM submission packages
• Ensure quality and completeness of SDTM format data

Main Responsibilities:

• Collaborate with Sponsor colleagues and CRO Partners to review SDTM
• In collaboration with Study Data Leads ensure the planning for data receipt and its oversight throughout the duration of assigned clinical trials
• Program reports and contribute to the standardization of process and reports used for data review and analysis for external partners/vendors and internal teams
• Complete formal and ad-hoc analyses and oversight of SDTM data.
• Review of critical document/deliverable (SDTM Annotation, SDTM datasets) to ensure Data Standards are used consistently and support creation of DE dataset
• Program either SDTM SAS PRD or SAS QC of some SDTM deliveries managed internally
• Attend meetings as applicable with Mission, Submission, Project, Program, JCST, DEM, Biometrics, Clinical & Regulatory Solutions Team (CRST), Early Phase
• Perform relevant quality checks and create standard edit checks for new CRF modules and share in the appropriate space
• Support audits and inspections as required and other responsibilities and projects that the Company may assign.

Experience Required:

• At least 5 years relevant SAS experience preferred
• Experience with Biometrics processes, to include:
• Review of SDTM annotated CRFs
• Writing and reviewing technical specifications
• Review of log files for errors and warnings
• Resolving/trouble shooting errors
• Experience with data mapping and SDTM Controlled Terminology
• Experience with SAS programming and SDTM deliveries
• Prior experience in a clinical or pharmaceutical related field is required.
• Prior experience in a Data Management related field is required
• Experience with relational databases, preferably Clinical Data Management and EDC Systems
• Advanced familiarity with reporting tools.
• Advanced knowledge of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices.
• Excellent command, both verbal and written, of English

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Role Overview:

• This unique role within IQVIA lends itself to a technically minded person with strong communication skills and SDTM knowledge. Having experience with SAS programming will be key for this position. The role can be based remotely from anywhere in Europe or in South Africa.
• This role is part of a sponsor dedicated project where you will be working with the client directly to manage Database SDTM Deliveries.
• The primary functions of this role will be to define SDTM specification and Programming including SDTM review ensuring quality and completeness of SDTM format data.

Primary Functions:

• Review and programming of SDTM deliveries
• Build and review SDTM submission packages
• Ensure quality and completeness of SDTM format data

Main Responsibilities:

• Collaborate with Sponsor colleagues and CRO Partners to review SDTM
• In collaboration with Study Data Leads ensure the planning for data receipt and its oversight throughout the duration of assigned clinical trials
• Program reports and contribute to the standardization of process and reports used for data review and analysis for external partners/vendors and internal teams
• Complete formal and ad-hoc analyses and oversight of SDTM data.
• Review of critical document/deliverable (SDTM Annotation, SDTM datasets) to ensure Data Standards are used consistently and support creation of DE dataset
• Program either SDTM SAS PRD or SAS QC of some SDTM deliveries managed internally
• Attend meetings as applicable with Mission, Submission, Project, Program, JCST, DEM, Biometrics, Clinical & Regulatory Solutions Team (CRST), Early Phase
• Perform relevant quality checks and create standard edit checks for new CRF modules and share in the appropriate space
• Support audits and inspections as required and other responsibilities and projects that the Company may assign.

Experience Required:

• At least 5 years relevant SAS experience preferred
• Experience with Biometrics processes, to include:
• Review of SDTM annotated CRFs
• Writing and reviewing technical specifications
• Review of log files for errors and warnings
• Resolving/trouble shooting errors
• Experience with data mapping and SDTM Controlled Terminology
• Experience with SAS programming and SDTM deliveries
• Prior experience in a clinical or pharmaceutical related field is required.
• Prior experience in a Data Management related field is required
• Experience with relational databases, preferably Clinical Data Management and EDC Systems
• Advanced familiarity with reporting tools.
• Advanced knowledge of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices.
• Excellent command, both verbal and written, of English

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Job Summary

• The Psychometric Properties Data Analyst Manager is a subject-matter expert in psychometric evaluation of Clinical Outcome Assessments (COAs). This role is responsible for the curation, maintenance, and enhancement of psychometric properties data within IQVIA’s COAA / COA Accelerator platform.
• The position requires advanced expertise in the development, validation, and evaluation of COA instruments, with a strong focus on measurement properties such as reliability, validity, and ability to detect change. The role plays a critical part in ensuring that psychometric data are robust, accurate, up-to-date, and fit-for-purpose for regulatory, scientific, and client use.

Required Skills & Competencies

• Deep expertise in psychometric principles applied to COAs.
• Strong analytical and critical appraisal skills.
• High attention to detail and data quality.
• Clear written and verbal communication skills.
• Ability to operate independently in a senior expert role.

Key Responsibilities

• Act as a recognized expert in psychometric properties of COAs.
• Curate, review, and maintain psychometric properties data within the COAA / COA Accelerator platform.
• Ensure completeness, methodological accuracy, and consistency of psychometric records.
• Collaborate with clinical, scientific, regulatory, and analytics stakeholders.
• Support client and internal discussions through expert interpretation of psychometric evidence.
• Contribute to continuous improvement of data models and standards related to psychometric properties.

Required Qualifications & Experience

• Advanced degree (PhD, MSc, or equivalent) in a relevant scientific field or equivalent professional experience.
• Significant hands-on experience in COA development and/or validation.
• Proven expertise in interpretation of psychometric analyses from literature and studies.
• Experience with structured data platforms or databases is strongly preferred.

go to method of application »

Job Summary

• The Psychometric Properties Data Analyst Manager is a subject-matter expert in psychometric evaluation of Clinical Outcome Assessments (COAs). This role is responsible for the curation, maintenance, and enhancement of psychometric properties data within IQVIA’s COAA / COA Accelerator platform.
• The position requires advanced expertise in the development, validation, and evaluation of COA instruments, with a strong focus on measurement properties such as reliability, validity, and ability to detect change. The role plays a critical part in ensuring that psychometric data are robust, accurate, up-to-date, and fit-for-purpose for regulatory, scientific, and client use.

Required Skills & Competencies

• Deep expertise in psychometric principles applied to COAs.
• Strong analytical and critical appraisal skills.
• High attention to detail and data quality.
• Clear written and verbal communication skills.
• Ability to operate independently in a senior expert role.

Key Responsibilities

• Act as a recognized expert in psychometric properties of COAs.
• Curate, review, and maintain psychometric properties data within the COAA / COA Accelerator platform.
• Ensure completeness, methodological accuracy, and consistency of psychometric records.
• Collaborate with clinical, scientific, regulatory, and analytics stakeholders.
• Support client and internal discussions through expert interpretation of psychometric evidence.
• Contribute to continuous improvement of data models and standards related to psychometric properties.

Required Qualifications & Experience

• Advanced degree (PhD, MSc, or equivalent) in a relevant scientific field or equivalent professional experience.
• Significant hands-on experience in COA development and/or validation.
• Proven expertise in interpretation of psychometric analyses from literature and studies.
• Experience with structured data platforms or databases is strongly preferred.

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Job Description

• Prepares and/or reviews regulatory documents to support clinical trial submissions. With guidance from senior staff, provides regulatory support for more complex projects.
• Acts as a Clinical Trial Regulatory Manager (CTRM) on straightforward projects independently and complex regulatory projects under the guidance of senior staff.
• Ability to administratively and technically/scientifically review core scientific documentation and feedback gap analysis to customers.
• Prepares and maintains core clinical trial submission dossiers in accordance with applicable regulatory requirements.
• Interacts with internal and external clients to provide regulatory guidance and strategic input for clinical trials.
• May strategically plan and perform/support European centralized submissions and facilitate global submissions with minimal supervision.
• Understands the Scope of Work, deliverables and budget for any given project and ensure timelines are met.
• Ensures high quality in all regulatory deliverables
• Ensures accurate completion, maintenance and adherence to internal systems, databases, tracking tools and project plans in line with agreed SOPs (customer and/or IQVIA).
• Ability to participate in audits relating to Projects and Systems.
• May perform additional tasks as deemed appropriate by Line Manager

Required Qualifications

• Bachelor's Degree Degree in Lifescience or related discipline
• At least 1-2 years relevant experience with EU CTIS, Global core pack knowledge
• Experience in country oversight particularly for amendments
• Good understanding of the Research and Development process (Chemistry, Manufacturing & Controls, Preclinical and Clinical), laws and related guidelines, as appropriate;
• Strong software and computer skills, including Microsoft Office, CTMS, SA WF, SAFE, Wingspan, as applicable;
• Possesses a specific regulatory or technical expertise;
• Good, solid interpersonal communication (oral and written) and organisation skills;
• Ability to establish and maintain effective working relationships with coworkers, managers and clients;
• Demonstrates self-motivation and enthusiasm;
• Ability to work on several projects, with direction from senior staff as appropriate;
• Ability to follow standard operating porcedures consistently; provides independent thought to assist in process improvements;
• Ability to make decisions on discrete tasks under senior supervision.

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Job Overview

• The Proposal Developer at IQVIA is responsible for developing high‑quality, accurate, and competitive proposals and budgets in response to client Requests for Proposal (RFPs). The role supports global Sales and Business Development teams and acts as a critical link between Sales, Operations, Strategic Pricing, Contracts, and Delivery functions to ensure proposals align with customer requirements, internal processes, and commercial objectives.

Key Responsibilities

• Review, analyze, and interpret RFPs, RFIs, and related client documentation to identify requirements for proposal narratives, scopes of work, and budget development.
• Develop and prepare comprehensive proposal texts, budgets, pricing models, rebids, and change orders that are accurate, compliant, and competitive.
• Collaborate closely with Sales, Business Development, Strategic Pricing, Contracts, and Operational Delivery teams throughout the proposal lifecycle.
• Develop or revise preliminary agreements, scopes of work, assumptions, and cost models, ensuring clear alignment between scope, deliverables, and pricing.
• Participate in proposal strategy calls to clarify customer requirements, resolve inconsistencies, and contribute to overall bid strategy.
• Perform thorough quality control, accuracy, and compliance reviews of proposal documents prior to submission.
• Maintain and update proposal-related data in corporate systems, CRM tools, templates, and tracking databases to ensure reporting accuracy and audit readiness.
• Support end‑to‑end proposal project management; at higher levels, independently lead proposal efforts and mentor junior proposal staff.
• Participate in customer meetings, bid defenses, and internal governance or review meetings as required.
• Contribute to departmental initiatives, process improvements, and best practice development.

Qualifications

• Bachelor’s degree in Life Sciences, Business, Finance, or a related field.
• Demonstrated experience in proposal development, pricing, contracts, or bid management, preferably in a CRO or clinical research environment.
• Strong understanding of proposal development processes, costing models, and commercial considerations.
• Experience interpreting RFPs, clinical protocols, scopes of work, and contractual requirements.
• Proficiency in Microsoft Office tools, particularly Excel and Word; experience with CRM or proposal management systems is an advantage.
• Strong analytical, organizational, and problem‑solving skills.
• Excellent written and verbal communication skills in English.
• Ability to manage multiple proposals simultaneously while meeting tight deadlines.
• Proven ability to build effective working relationships with cross‑functional stakeholders and senior internal customers.

Key Competencies

• Commercial and financial acumen
• Attention to detail and quality focus
• Stakeholder management
• Cross‑functional collaboration
• Ability to work in a fast‑paced, deadline‑driven environment
• Ownership and accountability

go to method of application »

Job Overview

• The Proposal Developer at IQVIA is responsible for developing high‑quality, accurate, and competitive proposals and budgets in response to client Requests for Proposal (RFPs). The role supports global Sales and Business Development teams and acts as a critical link between Sales, Operations, Strategic Pricing, Contracts, and Delivery functions to ensure proposals align with customer requirements, internal processes, and commercial objectives.

Key Responsibilities

• Review, analyze, and interpret RFPs, RFIs, and related client documentation to identify requirements for proposal narratives, scopes of work, and budget development.
• Develop and prepare comprehensive proposal texts, budgets, pricing models, rebids, and change orders that are accurate, compliant, and competitive.
• Collaborate closely with Sales, Business Development, Strategic Pricing, Contracts, and Operational Delivery teams throughout the proposal lifecycle.
• Develop or revise preliminary agreements, scopes of work, assumptions, and cost models, ensuring clear alignment between scope, deliverables, and pricing.
• Participate in proposal strategy calls to clarify customer requirements, resolve inconsistencies, and contribute to overall bid strategy.
• Perform thorough quality control, accuracy, and compliance reviews of proposal documents prior to submission.
• Maintain and update proposal-related data in corporate systems, CRM tools, templates, and tracking databases to ensure reporting accuracy and audit readiness.
• Support end‑to‑end proposal project management; at higher levels, independently lead proposal efforts and mentor junior proposal staff.
• Participate in customer meetings, bid defenses, and internal governance or review meetings as required.
• Contribute to departmental initiatives, process improvements, and best practice development.

Qualifications

• Bachelor’s degree in Life Sciences, Business, Finance, or a related field.
• Demonstrated experience in proposal development, pricing, contracts, or bid management, preferably in a CRO or clinical research environment.
• Strong understanding of proposal development processes, costing models, and commercial considerations.
• Experience interpreting RFPs, clinical protocols, scopes of work, and contractual requirements.
• Proficiency in Microsoft Office tools, particularly Excel and Word; experience with CRM or proposal management systems is an advantage.
• Strong analytical, organizational, and problem‑solving skills.
• Excellent written and verbal communication skills in English.
• Ability to manage multiple proposals simultaneously while meeting tight deadlines.
• Proven ability to build effective working relationships with cross‑functional stakeholders and senior internal customers.

Key Competencies

• Commercial and financial acumen
• Attention to detail and quality focus
• Stakeholder management
• Cross‑functional collaboration
• Ability to work in a fast‑paced, deadline‑driven environment
• Ownership and accountability