IQVIA
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Clinical Study Manager
role at
IQVIA .
Job Overview
Accountable for regional study delivery with appropriate inspection readiness quality, within agreed timelines and budget.
Leads the regional clinical operations team (including oversight of external partners) and serves as escalation point for issue resolution within the region for the assigned study.
Ensures alignment of regional deliverables with overall study goals.
Essential Functions
Leads the regional clinical operations team effectively, ensuring effective decision‑making and acts as escalation point for issue resolution.
Collaborates with key regional stakeholders, providing regular updates on study progress to senior management and the Global Clinical Study Manager as required.
Manages regional study budgets and monitors resource utilization over the study lifecycle, liaising with functional managers as needed.
Plans and manages the assigned clinical study(ies) from feasibility through close‑out for the region, in line with global study timelines.
Ensures operational feasibility in the region, driving trial feasibility, country allocation, and site selection processes in collaboration with feasibility managers, country heads, medical affairs, and other stakeholders.
Prepares sites for quality‑assurance audits and inspections, drives responses to audit and inspection findings as appropriate.
Collaborates closely with CRAs in the region to ensure proper study execution at the sites; reviews and signs off monitoring reports.
Experience Requirements
Bachelor's Degree required.
4 or more years of progressive experience in clinical research within biotech, pharma, or CRO industry.
Proven experience in clinical research including relevant experience as a team lead in clinical functions.
Experience as CRA preferred.
Recent (within 1–2 years) oncology experience as a study manager, focused in solid‑tumor or hematological oncology studies.
Experience with site management and engagement.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
Location: Durham, NC
The potential base pay range for this role, when annualized, is $93,100.00 – $232,800.00. The actual base pay offered may vary based on a number of factors including job‑related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part‑time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
Seniority level: Mid‑Senior level
Employment type: Full‑time
Job function: Research, Analyst, and Information Technology; Industries: Hospitals and Health Care.
IQVIA is proud to be an equal‑opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
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Clinical Study Manager
role at
IQVIA .
Job Overview
Accountable for regional study delivery with appropriate inspection readiness quality, within agreed timelines and budget.
Leads the regional clinical operations team (including oversight of external partners) and serves as escalation point for issue resolution within the region for the assigned study.
Ensures alignment of regional deliverables with overall study goals.
Essential Functions
Leads the regional clinical operations team effectively, ensuring effective decision‑making and acts as escalation point for issue resolution.
Collaborates with key regional stakeholders, providing regular updates on study progress to senior management and the Global Clinical Study Manager as required.
Manages regional study budgets and monitors resource utilization over the study lifecycle, liaising with functional managers as needed.
Plans and manages the assigned clinical study(ies) from feasibility through close‑out for the region, in line with global study timelines.
Ensures operational feasibility in the region, driving trial feasibility, country allocation, and site selection processes in collaboration with feasibility managers, country heads, medical affairs, and other stakeholders.
Prepares sites for quality‑assurance audits and inspections, drives responses to audit and inspection findings as appropriate.
Collaborates closely with CRAs in the region to ensure proper study execution at the sites; reviews and signs off monitoring reports.
Experience Requirements
Bachelor's Degree required.
4 or more years of progressive experience in clinical research within biotech, pharma, or CRO industry.
Proven experience in clinical research including relevant experience as a team lead in clinical functions.
Experience as CRA preferred.
Recent (within 1–2 years) oncology experience as a study manager, focused in solid‑tumor or hematological oncology studies.
Experience with site management and engagement.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
Location: Durham, NC
The potential base pay range for this role, when annualized, is $93,100.00 – $232,800.00. The actual base pay offered may vary based on a number of factors including job‑related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part‑time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
Seniority level: Mid‑Senior level
Employment type: Full‑time
Job function: Research, Analyst, and Information Technology; Industries: Hospitals and Health Care.
IQVIA is proud to be an equal‑opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
#J-18808-Ljbffr