IQVIA · 17 hours ago
Clinical Study Manager
Durham, NC
Full-time
Onsite
Mid, Senior Level
$93K/yr - $233K/yr
4+ years expIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. The Clinical Study Manager will be responsible for regional study delivery, leading clinical operations teams, managing budgets, and ensuring alignment with study goals.
AnalyticsHealth CareLife Science
Responsibilities
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 working on the regional level) and acts as point of escalation for resolution of issues within the region for the assigned study
Ensures alignment of regional deliverables with overall study goals
Leads the regional clinical operations team effectively, ensures effective decision making and acts as point of escalation for resolution of issues within the region for the assigned study
Collaborates with key stakeholders in the region and provides regular updates on study progress in the region to senior management and Global Clinical Study Manager as required
Manages regional study budgets
Monitors regional resource utilization over study lifecycle and liaises with functional managers as needed
Leads planning and management of the assigned clinical study(ies) from feasibility through closeout activities for region, in line with global study timelines
Ensures that the clinical study is operationally feasible in the region, drives trial feasibility, country allocation and site selection process for assigned region in collaboration with feasibility managers, country heads, medical affairs and any 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
Qualification
Required
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 team lead in clinical functions
Experience with site management and engagement
Preferred
Experience as CRA is preferred
Recent (within 1-2 years) oncology experience as a study manager. Focused in solid tumor or hematological oncology studies
Benefits
Incentive plans
Bonuses
Health and welfare and/or other benefits
Company
IQVIA
IQVIA provides analytics, compliance, and management solutions to the life sciences industry.
10001+ employees
H1B Sponsorship
IQVIA has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (167)
2024 (294)
2023 (261)
2022 (229)
2021 (208)
2020 (180)
Funding
Current Stage
Public CompanyTotal Funding
$3.5B2025-06-02Post Ipo Debt· $2B
2023-11-14Post Ipo Debt· $500M
2023-05-18Post Ipo Debt· $1B
Leadership Team
Chris Colapietro
Vice President, Customer Engagement
Jonathan Morris
VP & GM US Healthcare
Recent News
Sabin Vaccine Institute
2025-12-04
Company data provided by crunchbase