Latest Jobs at IQVIA

Duties/Responsibilities:

• Act as signal detection and literature lead, or back-up lead to contribute to the conduct of ongoing literature safety surveillance for marketed and investigational products, evaluating events of special interests as well as aggregate data review
• Author and finalize aggregate reports, including but not limited to PBRERs/PSUR, DSURs and ACOs.
• Author responses to regulatory agency/ Pharmacovigilance Risk Assessment Committee (PRAC) inquiries, as required.
• Can serve as principal owner (molecule lead) for the molecule and have responsibility for completion of the deliverable and in compliance with all applicable Key performance indicators (KPI); Set-up and update products' signaling strategies, as approved by the customer’s Safety Strategy Lead. Author and/or QC review all types of signal management deliverables. Lead/ conduct ongoing signal detection activities as per agreed signaling strategies, perform signal validation and signal evaluation analyses for proactive and timely identification of signals and characterization of risks, as approved by the customer’s Safety Strategy Lead. Responsible for full documentation and tracking of signals.
• Ensuring the completion of molecule deliverables on time and liaise with portfolio clinical science scientists, service provider process leads and cross-functional stakeholders.
• Distribution of molecule work within team consisting of molecule scientists, when necessary, coordinating support across molecules and disease areas when there are peaks and troughs in workload.
• End-to-end molecule work oversight and responsibility (i.e., ensuring consistent tracking of signals from detection to assessment to inclusion in aggregate reports).
• Ensuring an in-depth knowledge of the molecule and disease area within the service provider molecule team.
• Oversight and responsibility of quality-of molecule deliverables to the customer’s molecule team, with “hands-on” involvement, i.e., involved in authoring DSR conclusion, participating in SD/Lit meetings between service provider and customers.
• Responsible for resolution of issues on molecule deliverables (if necessary, in collaboration with service provider process lead).
• Participate in internal and external audits and inspections, as required.
• Read, acknowledge and adhere to all necessary IQVIA standard operating procedures (SOPs) and customer SOPs as required. Ensure all required training is executed in a timely fashion to maintain compliance and documented
• Conduct regular lessons learned with the working teams to ensure all information from the customer is cascaded to the relevant team members.

Qualifications:

• Life science graduate/post-graduate, pharmacy, nursing, other healthcare related qualification or experience in pharmacovigilance
• 4-6 years of relevant experience in Pharmacovigilance including hands-on experience of drug safety, aggregate reports, signal detection/signal management preferred
• Excellent communication (written and verbal) skills
• Team working
• English – fluent (spoken, written)
   

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Job Overview

• Provide advanced technical expertise to develop, maintain, and support programs that meet internal and external client needs. Plan and lead the development of project-related solutions covering the full scope of statistical programming activities. Serve as a technical resource within the Statistical Programming department.

Essential Functions

• Plan, perform, test, and document programs used to produce statistical tables, figures, and listings.
• Program analysis databases (derived datasets) and manage data transfers for internal and external clients.
• Plan and perform database quality control and validation activities, as required.
• Program the integration of databases from multiple studies or data sources.
• Develop and maintain programming documentation, including plans and specifications, as appropriate.
• Provide advanced technical expertise to internal and external stakeholders and independently deliver project solutions to teams and the department.
• Plan, develop, implement, and validate new processes, technologies, macros, and applications.
• Fulfill project responsibilities at the level of statistical team lead for single studies, under supervision.
• Understand project Scope of Work, estimate completed effort, and manage out-of-scope activities for single studies.
• May manage budgets and resource requirements, and provide revenue and resource forecasts for single studies.
• May be required to understand and apply budgeting and quoting assumptions.
• Provide training, mentorship, and guidance to junior and newly onboarded staff.

Qualifications

• Master’s degree in Computer Science or a related field with a minimum of one year of relevant experience, or
• Bachelor’s degree in Computer Science or a related field with a minimum of two years of relevant experience, or
• An equivalent combination of education, training, and experience.
• Knowledge of statistics, programming, and/or the clinical drug development process.
• Working knowledge of computing applications, including Base SAS, SAS/STAT, and SAS Macro Language.
• Strong organizational, interpersonal, leadership, and communication skills.
• Ability to manage multiple tasks and projects effectively.
• Excellent attention to detail and accuracy.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

go to method of application »

Job Overview

• Provide advanced technical expertise to develop, maintain, and support programs that meet internal and external client needs. Plan and lead the development of project-related solutions covering the full scope of statistical programming activities. Serve as a technical resource within the Statistical Programming department.

Essential Functions

• Plan, perform, test, and document programs used to produce statistical tables, figures, and listings.
• Program analysis databases (derived datasets) and manage data transfers for internal and external clients.
• Plan and perform database quality control and validation activities, as required.
• Program the integration of databases from multiple studies or data sources.
• Develop and maintain programming documentation, including plans and specifications, as appropriate.
• Provide advanced technical expertise to internal and external stakeholders and independently deliver project solutions to teams and the department.
• Plan, develop, implement, and validate new processes, technologies, macros, and applications.
• Fulfill project responsibilities at the level of statistical team lead for single studies, under supervision.
• Understand project Scope of Work, estimate completed effort, and manage out-of-scope activities for single studies.
• May manage budgets and resource requirements, and provide revenue and resource forecasts for single studies.
• May be required to understand and apply budgeting and quoting assumptions.
• Provide training, mentorship, and guidance to junior and newly onboarded staff.

Qualifications

• Master’s degree in Computer Science or a related field with a minimum of one year of relevant experience, or
• Bachelor’s degree in Computer Science or a related field with a minimum of two years of relevant experience, or
• An equivalent combination of education, training, and experience.
• Knowledge of statistics, programming, and/or the clinical drug development process.
• Working knowledge of computing applications, including Base SAS, SAS/STAT, and SAS Macro Language.
• Strong organizational, interpersonal, leadership, and communication skills.
• Ability to manage multiple tasks and projects effectively.
• Excellent attention to detail and accuracy.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
   

go to method of application »

Job Overview

• Provide advanced technical expertise to develop, maintain, and support programs that meet internal and external client needs. Plan and lead the development of project-related solutions covering the full scope of statistical programming activities. Serve as a technical resource within the Statistical Programming department.

Essential Functions

• Plan, perform, test, and document programs used to produce statistical tables, figures, and listings.
• Program analysis databases (derived datasets) and manage data transfers for internal and external clients.
• Plan and perform database quality control and validation activities, as required.
• Program the integration of databases from multiple studies or data sources.
• Develop and maintain programming documentation, including plans and specifications, as appropriate.
• Provide advanced technical expertise to internal and external stakeholders and independently deliver project solutions to teams and the department.
• Plan, develop, implement, and validate new processes, technologies, macros, and applications.
• Fulfill project responsibilities at the level of statistical team lead for single studies, under supervision.
• Understand project Scope of Work, estimate completed effort, and manage out-of-scope activities for single studies.
• May manage budgets and resource requirements, and provide revenue and resource forecasts for single studies.
• May be required to understand and apply budgeting and quoting assumptions.
• Provide training, mentorship, and guidance to junior and newly onboarded staff.

Qualifications

• Master’s degree in Computer Science or a related field with a minimum of one year of relevant experience, or
• Bachelor’s degree in Computer Science or a related field with a minimum of two years of relevant experience, or
• An equivalent combination of education, training, and experience.
• Knowledge of statistics, programming, and/or the clinical drug development process.
• Working knowledge of computing applications, including Base SAS, SAS/STAT, and SAS Macro Language.
• Strong organizational, interpersonal, leadership, and communication skills.
• Ability to manage multiple tasks and projects effectively.
• Excellent attention to detail and accuracy.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

go to method of application »

• Clinical Project Management, IQVIA Biotech is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads can run their own studies. The Project Lead focus is on leveraging therapeutic expertise and IQVIA’s suite of solutions to drive operational excellence and strategic leadership with our customers.

Main Responsibilities

• Accountable for the execution of clinical studies, or assigned portion of clinical studies, per contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.
• Set objectives of the core project team according to agreed upon contract, strategy and approach, effectively communicate and assess performance.
• Participate in bid defense presentations in partnership with Business Development and may lead the presentation for smaller, less complex regional studies.
• May be responsible for delivery and management of smaller, less complex, regional studies.
• Develop integrated study management plans with the core project team.
• Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.
• Monitor progress against contract and prepare project information proactively to stakeholders internally and externally.
• Manage risk (positive and negative) and contingencies proactively and lead problem solving and resolution efforts.
• Achieve project quality by identifying quality risks and issues, responding to issues raised by project team and implementing appropriate corrective and preventative action plans.
• May serve as primary or backup project contact with customer and would then own the relationship with the project’s key customer contacts, as well as collaborate with IQVIA business development representatives.
• Build the cross-functional project team and lead their efforts; responsible for managing cross-collaboration of the core team and for overall project delivery to support milestone achievement and to manage study issues and obstacles.
• Ensure the financial success of the project.
• Forecast and identify opportunities to accelerate activities to bring revenue forward.
• Identify changes in scope and manage change control process as necessary.
• Provide input to line managers of their project team members’ performance relative to project tasks.
• Support staff development and mentor less experienced project team members on assigned projects to support their professional development.

Required Skills and Qualifications

• Bachelor's Degree Life sciences or related field.
• 5 years of prior relevant experience including > 1 years project management experience or equivalent combination of education, training and experience.
• Advanced knowledge of job area, typically obtained through advanced education combined with experience.
• Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct.
• Broad protocol knowledge; therapeutic area knowledge in any of the following would be an advantage: cardiovascular - metabolic, renal, obesity.
• Good understanding of project financials including experience managing, contractual obligations and implications.
• Good understanding of the competitive environment and how to communicate value through IQVIA Biotech solutions.
• Strong written and verbal communication skills including very good command of English language.
• Strong customer service skills and presentation abilities.
• Ability to work through others to deliver results to the appropriate quality and timeline metrics, monitoring performance and providing feedback, experience productively partnering cross functionally and with customers to advance work effectively and efficiently.
• Ability to make decisions, bringing clarity to disparate information to inform actions and drive results.
• Planning, time management and prioritization skills.
• Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances.
• Results-oriented approach to work towards delivery and output.
• Demonstrated learning agility and openness to learning and keeping own knowledge and skill set current and evolving.
• Good software and computer skills.
• Ability to work across geographies displaying high awareness and understanding of cultural differences.
• May require occasional travel to the United States.

go to method of application »

• Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads can run their own studies. The Project Lead focus is on leveraging therapeutic expertise and IQVIA’s suite of solutions to drive operational excellence and strategic leadership with our customers

Essential Functions

• Participate in bid defense presentations in partnership with Business Development and may lead the presentation for smaller, less complex regional studies.
• May be responsible for delivery and management of smaller, less complex, regional studies.
• Develop integrated study management plans with the core project team.
• Accountable for the execution of clinical studies, or assigned portion of clinical studies, per contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.
• Set objectives of the core project team and/or sub-team(s) according to agreed upon contract, strategy and approach, effectively communicate and assess performance.
• Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.
• Monitor progress against contract and prepare/present project and/or sub-team information proactively to stakeholders internally and externally.
• Manage risk (positive and negative) and contingencies proactively and lead problem solving and resolution efforts.
• Achieve project quality by identifying quality risks and issues, responding to issues raised by project team and/or sub-team members and planning/implementing appropriate corrective and preventative action plans.
• May serve as primary or backup project contact with customer and would then own the relationship with the project’s key customer contacts, as well as communicate/collaborate with IQVIA business development representatives, as necessary.;
• Build the cross-functional project team and lead their efforts; responsible for managing cross-collaboration of the core team and for overall project delivery to support milestone achievement and to manage study issues and obstacles.;
• Ensure the financial success of the project.
• Forecast and identify opportunities to accelerate activities to bring revenue forward.
• Identify changes in scope and manage change control process as necessary.
• Identify lessons learned and implement best practices.
• May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements.;
• Adopt corporate initiatives and changes and serve as a change advocate when necessary.
• Provide input to line managers of their project team members’ performance relative to project tasks.
• Support staff development and mentor less experienced project team members on assigned projects to support their professional development.;

Qualifications

• Bachelor's Degree Life sciences or related field
• 5 years of prior relevant experience including > 1 years project management experience or equivalent combination of education, training and experience.
• Advanced knowledge of job area, and broad knowledge of other related job areas, typically obtained through advanced education combined with experience.
• Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct.

go to method of application »

• Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads can run their own studies. The Project Lead focus is on leveraging therapeutic expertise and IQVIA’s suite of solutions to drive operational excellence and strategic leadership with our customers

Essential Functions

• Participate in bid defense presentations in partnership with Business Development and may lead the presentation for smaller, less complex regional studies.
• May be responsible for delivery and management of smaller, less complex, regional studies.
• Develop integrated study management plans with the core project team.
• Accountable for the execution of clinical studies, or assigned portion of clinical studies, per contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.
• Set objectives of the core project team and/or sub-team(s) according to agreed upon contract, strategy and approach, effectively communicate and assess performance.
• Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.
• Monitor progress against contract and prepare/present project and/or sub-team information proactively to stakeholders internally and externally.
• Manage risk (positive and negative) and contingencies proactively and lead problem solving and resolution efforts.
• Achieve project quality by identifying quality risks and issues, responding to issues raised by project team and/or sub-team members and planning/implementing appropriate corrective and preventative action plans.
• May serve as primary or backup project contact with customer and would then own the relationship with the project’s key customer contacts, as well as communicate/collaborate with IQVIA business development representatives, as necessary.;
• Build the cross-functional project team and lead their efforts; responsible for managing cross-collaboration of the core team and for overall project delivery to support milestone achievement and to manage study issues and obstacles.;
• Ensure the financial success of the project.
• Forecast and identify opportunities to accelerate activities to bring revenue forward.
• Identify changes in scope and manage change control process as necessary.
• Identify lessons learned and implement best practices.
• May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements.;
• Adopt corporate initiatives and changes and serve as a change advocate when necessary.
• Provide input to line managers of their project team members’ performance relative to project tasks.
• Support staff development and mentor less experienced project team members on assigned projects to support their professional development.;

Qualifications

• Bachelor's Degree Life sciences or related field
• 5 years of prior relevant experience including > 1 years project management experience or equivalent combination of education, training and experience.
• Advanced knowledge of job area, and broad knowledge of other related job areas, typically obtained through advanced education combined with experience.
• Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct.

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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

Why Join IQVIA?

• Become part of a leading organization in commercial and medical solutions
• Work with premium dental brands and innovative commercial strategies
• 1-year contract with strong potential for renewal based on performance
• Significant opportunities for development, upskilling, and career advancement
• Gain exposure to a diverse, high-growth healthcare environment

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About the Role:

• We are seeking a seasoned Public Health professional with deep expertise in market access, policy development, and funding mobilization to join the Market Access Team. This role is pivotal in enabling access to our diagnostic portfolio by navigating policy landscapes, engaging stakeholders, sourcing mobilizing alternative funding streams and applying health economic evidence to inform adoption and scape up decisions. The successful candidate will have a strong network within Ministries of Health and related institutions in Portuguese-speaking Sub-Saharan Africa, particularly Mozambique and Angola.

Key Responsibilities:

• Develop and execute market access strategies for current and future diagnostic products.
• Identify and address policy barriers affecting product adoption and commercialization.
• Engage with government bodies, NGOs, policy makers, and program implementers to influence health policy.
• Lead advocacy efforts and generate evidence to support favourable regulatory environments.
• Collaborate cross-functionally with Commercial, Marketing, Medical, and Sales teams.
• Identify and support funding opportunities for new and existing projects.
• Identify, assess and pursue alternative funding opportunities (donors, multilateral agencies, PP)
• Monitor and report on funding landscape and donor priorities Iin both countries
• Maintain strong relationships with Ministries of Health and other key stakeholders.
• Travel extensively across Mozambique and Angola to support program implementation.
• Act as the focal point for engagement with donors, implementing partners and advocacy groups

Key Qualifications:

• Bachelor’s or master’s degree in Public health, International Development, Health Economics, Policy, or related field.
• Minimum of 5–10 years’ experience in public health, market access, health policy, donor engagement, public health program management and funding/resource mobilization.
• strong track record of mobilizing alternative funding sources
• Experience generating or applying health economic evidence to inform policy and program decisions
• Deep understanding of the public health landscape in Portuguese-speaking Sub-Saharan Africa.
• Strong network and experience working with Ministries of Health and other government institutions.
• Willingness and ability to travel extensively and on short notice.
• Fluent in Portuguese and English.

Preferred Candidate Profile:

• Based in Mozambique.
• Strategic thinker with hands-on experience in market access and policy advocacy.
• Excellent communication and stakeholder engagement skills.
• Results-driven and adaptable to dynamic environments.
• Strong analytical and problem-solving skills with the ability to translate complex data into actionable insights
• Ability to work independently and collaboratively in multicultural team