Top 367 Clinical study manager Jobs in Durham Nc

Senior Global Clinical Study Manager
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Customer service
- Bachelor's degree
- Continuous improvement
Senior Clinical Trial Manager - CNS - U.S. (Remote)
Worldwide Clinical Trials —Research Triangle Park, NC
- $112,000 - $222,000 a year
- Full-time
- Remote
- Nursing
- English
- Bachelor's degree
Clinical Project Manager (US)
Alimentiv —Raleigh-Durham, NC
- $95,500 - $159,000 a year
- Full-time
- Remote
- English
- Mid-level
- Bachelor's degree
Quick Apply
Clinical Trial Manager - CAR T or Ophthalmology
Fortrea —Durham, NC
- $140,000 - $148,000 a year
- Full-time
- Remote
- English
- 3 years
- Master's degree
Manager, Clinical Operations
IQVIA —Durham, NC
- $86,500 - $216,000 a year
- Full-time
- Microsoft Excel
- English
- Mid-level
Senior Clinical Data Manager
Fortrea —Durham, NC
- $85,000 - $120,000 a year
- Full-time
- Remote
- Customer service
- English
- Bachelor's degree
- Disability insurance
- Health insurance
1d
RWE Clinical Project Manager – Oncology (FSP)
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Mid-level
- Bachelor's degree
- Continuous improvement
Senior Clinical Research Associate - US
Optimapharm d.o.o. —Durham, NC
- $100,000 - $130,000 a year
- Full-time
- Remote
- Nursing
- 5 years
- Computer literacy
- Dental insurance
- Paid time off
14d
Clinical Research Associate 2, IQVIA
IQVIA —Durham, NC
- $71,900 - $189,000 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
Clinical Project Manager- IVD
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Bachelor's degree
- 1 year
- Senior level
Clinical Project Manager
Pluto Health —Durham, NC
- $85,000 - $120,000 a year
- Full-time
- 3 years
- Analysis skills
- Senior level
- Paid holidays
- Health insurance
Clinical Trials Manager
Kite Pharma —Raleigh, NC
- $133,195 - $189,640 a year
- Full-time
- 6 years
- Surgery
- RN License
- Health insurance
- Dental insurance
Clinical Research Associate II/III - US
Optimapharm d.o.o. —Durham, NC
- $75,000 - $100,000 a year
- Full-time
- Remote
- Nursing
- Computer literacy
- Mid-level
- Dental insurance
- Paid time off
14d
Senior Clinical Trial Manager
Worldwide Clinical Trials —Durham, NC
- $112,000 - $222,000 a year
- Full-time
- Nursing
- English
- Driver's License
1d
Senior Clinical Project Manager, Immuno-Oncology, IQVIA Biotech
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- 7 years
- Microsoft Office
- Bachelor's degree
6d
QA Manager, GCP
Sobi —Morrisville, NC
- $112,000 - $153,000 a year
- Full-time
- Remote
- 5 years
- Senior level
- Health insurance
Quick Apply
1d
Clinical Project Manager, Immuno-Oncology - IQVIA Biotech
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Customer service
- Bachelor's degree
- Continuous improvement
Global Clinical Operations Leader / Clinical Trial Manager
Parexel —Durham, NC
- Remote
- Nursing
- 5 years
- Continuous improvement
Clinical Project Manager - Oncology (Client Dedicated/Remote)
サイネオス・ヘルス —Morrisville, NC
- $120,000 - $135,000 a year
- Remote
- Mid-level
- 3 years
- Bachelor's degree
- Employee stock purchase plan
- Health insurance
Senior Clinical Project Manager
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Bachelor's degree
- Mentoring
- Senior level
2d

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Senior Global Clinical Study Manager

IQVIA -
Durham, NC

Apply Now

Job Details

Full-time
$93,100 - $232,800 a year

Qualifications

Clinical program budget management
Customer communication
Regulatory compliance
Global team management
ICH guidelines
Bachelor's degree
Project management experience in healthcare
Managing clinical research teams
Oncology research
Healthcare financial management
Clinical quality assurance standards
Oncology
Healthcare compliance
Operational budget management
Leading research teams
FDA regulations
Stakeholder management

Full Job Description

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.

Drive global clinical trials from first site activation to final patient visit—own the strategy, accelerate delivery, and shape the future of clinical research worldwide.

Required Experience

✅ 2+ years of global study management experience
✅ Experience across multiple countries/regions
✅ Phase I–III clinical trials experience (Phase III required)
✅ Oncology experience required
✅ Ability to work across multiple therapeutic areas

Job Overview

We are seeking a Global Study Manager responsible for the end-to-end planning, execution, and delivery of clinical trial site management activities across global studies. This role ensures successful site selection, activation, monitoring oversight, and closeout—while balancing speed, quality, and cost. You will serve as the primary point of contact for clients, lead cross-functional teams, and ensure compliance with ICH-GCP, regulatory requirements, and study protocols. This is a highly visible role that combines strategic leadership, operational execution, and financial oversight.

Key Responsibilities

Global Study & Site Leadership

Lead site management strategy from study award through close-out
Oversee site identification, selection, activation, and recruitment performance
Ensure clinical monitoring processes meet study needs and timelines
Partner with CRAs to optimize enrollment, data quality, and compliance

Project & Stakeholder Management

Serve as primary client contact and own key customer relationships
Lead cross-functional teams across regions and cultures
Facilitate internal and external meetings, including executive presentations
Drive collaboration across stakeholders, vendors, and functional leads

Operational Excellence & Risk Management

Develop and manage integrated study plans and risk mitigation strategies
Proactively identify risks and implement corrective/preventative actions
Monitor study timelines, enrollment trends, and data quality metrics
Ensure compliance with GCP, SOPs, protocols, and regulatory standards

Financial & Contract Management

Manage study financials, including forecasting and revenue acceleration
Identify and manage out-of-scope work and change orders
Oversee Billing Unit Reviews (BURs) and expense approvals
Track performance against budget and Estimate at Completion (EAC)

Quality & Compliance

Maintain TMF health and ensure timely document submission
Develop quality monitoring plans and compliance metrics
Ensure adherence to study tools, training materials, and processes

Team Leadership & Development

Lead and mentor cross-functional project teams
Support CRA and team training on therapeutic areas and study-specific needs
Foster collaboration, knowledge sharing, and continuous improvement

Qualifications

Required

Bachelor’s degree in life sciences or related field
5+ years of clinical research/monitoring experience, including 2 years in a clinical study management role
Strong knowledge of ICH-GCP, FDA regulations, and clinical trial processes
Experience managing global clinical trials and multi-regional teams
Demonstrated experience in project financial management

Core Competencies

Exceptional communication and stakeholder management skills
Strong problem-solving and risk mitigation capabilities
Ability to influence without authority in matrix organizations
High attention to detail and quality-driven mindset
Proficiency in Microsoft Office and clinical systems (e.g., CTMS, EDC)

Why Join Us

Work on cutting-edge global trials across therapeutic areas
Collaborate with top talent in a dynamic, global environment
Make a direct impact on patient outcomes worldwide

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

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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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.

Apply Now

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Required Experience

Job Overview

Key Responsibilities

Global Study & Site Leadership

Project & Stakeholder Management

Operational Excellence & Risk Management

Financial & Contract Management

Quality & Compliance

Team Leadership & Development

Qualifications

Required

Core Competencies

Why Join Us