Top 121 Clinical study manager Jobs in North Carolina

Clinical Project Manager- IVD
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Remote
- Bachelor's degree
- 1 year
- Senior level
- Work from home
RWE Clinical Project Manager (FSP)
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Remote
- Mid-level
- Bachelor's degree
- Continuous improvement
- Work from home
Manager, Site Contracts with Clinical Trials experience Hybrid or Remote in USA-NC
Syneos - Clinical and Corporate - Prod —Morrisville, NC
- $79,800 - $139,600 a year
- Full-time
- Remote
- Nursing
- Bachelor's degree
- Continuous improvement
- Employee stock purchase plan
- Health insurance
4d
Clinical Project Manager, Immuno-Oncology - IQVIA Biotech
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Remote
- Customer service
- Bachelor's degree
- Continuous improvement
- Work from home
Associate Clinical Project Manager, Immuno-Oncology, Cell and Gene Therapy, IQVIA Biotech
IQVIA —Durham, NC
- $68,400 - $171,000 a year
- Full-time
- Remote
- Mid-level
- Bachelor's degree
- Organizational skills
- Work from home
1d
Clinical Sr Project Manager / Assoc Director (Global role, Multisponsor) ** Remote US & Canada **
Syneos - Clinical and Corporate - Prod —North Carolina
- Up to $210,900 a year
- Full-time
- Remote
- Nursing
- Medicine
- Bachelor's degree
- Employee stock purchase plan
- Health insurance
Associate Clinical Lead Director
IQVIA —Durham, NC
- $102,500 - $285,500 a year
- Full-time
- Remote
- Microsoft Excel
- English
- Bachelor's degree
- Work from home
Manager Clinical Research
Cone Health —Greensboro, NC
- Bachelor's degree
- Team management
- Senior level
Senior Clinical Project Manager, Immuno-Oncology, IQVIA Biotech
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Remote
- 7 years
- Microsoft Office
- Bachelor's degree
- Work from home
Senior Global Clinical Study Manager
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Remote
- Bachelor's degree
- Continuous improvement
- Mentoring
- Work from home
Study Start-up and Regulatory Manager
Pedestal Health —Research Triangle Park, NC
- Hybrid work
- Mid-level
- Office
- 3 years
- Paid parental leave
- Health insurance
10d
Clinical Trial Manager - Full Service
サイネオス・ヘルス —North Carolina
- Remote
- Computer literacy
- Bachelor's degree
- Travel
- Employee stock purchase plan
- Health insurance
Clinical Trial Manager - Full Service
Syneos - Clinical and Corporate - Prod —North Carolina
- Full-time
- Computer literacy
- Bachelor's degree
- Travel
- Employee stock purchase plan
- Health insurance
Clinical Trial Manager - CAR T or Ophthalmology
Fortrea —Durham, NC
- $76,000 - $148,000 a year
- Full-time
- Remote
- English
- 3 years
- Master's degree
Study Manager - Vaccine
サイネオス・ヘルス —North Carolina
- Remote
- Nursing
- Medicine
- Bachelor's degree
- Employee stock purchase plan
- Health insurance
Clinical Study Design Manager
Science 37 —Raleigh, NC
- Remote
- Mid-level
- Analysis skills
- Bachelor's degree
Quick Apply
11d
Lead Data Manager
IQVIA —Durham, NC
- $89,900 - $224,500 a year
- Full-time
- Remote
- 7 years
- Senior level
- Leadership
- Work from home
Study Manager - Ophthalmology
サイネオス・ヘルス —North Carolina
- Remote
- Nursing
- Medicine
- Bachelor's degree
- Employee stock purchase plan
- Health insurance
Clinical Project Manager - Oncology (Client Dedicated/Remote)
サイネオス・ヘルス —North Carolina
- $120,000 - $135,000 a year
- Remote
- Mid-level
- 3 years
- Bachelor's degree
- Employee stock purchase plan
- Health insurance
Senior Clinical Project Manager- CNS
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Remote
- Microsoft Excel
- English
- Bachelor's degree
- Work from home

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clinical study manager jobs near north carolina

Clinical Project Manager- IVD

IQVIA -
Durham, NC

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Job Details

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

Benefits

Work from home

Qualifications

Product development projects
Project management experience in healthcare
Biomedical regulatory compliance
Regulatory submissions
Managing projects
Cross-functional team management
Cross-functional communication

Full Job Description

Durham, United States of America | Full time | Home-based | R1556598

Job Summary

The Project Lead is responsible for ensuring that all studies are designed, planned, executed, monitored, closed out and documented in an appropriate manner within the planned timeframe and cost; ensuring that the sponsor responsibilities are fulfilled, while assuring compliance to all applicable regulatory requirements. Responsible for the timeline and budget planning and execution of studies. Assigns and ensures delivery of specific tasks to/from other members of the study team. Provides oversight to outside support including CROs, consultants and/or medical advisors.

Responsibilities

Leading the global study team with full accountability for study deliverables regarding quality, budget, and timelines.
Developing key study documents (e.g., Design Validation Plan, protocol, study training materials, study forms and templates, study report).
Overseeing planning and operational aspects of companion diagnostics studies sponsored by Pharma partners.
Ensuring adherence to regulations, guidelines, and standard operating procedures, and ensuring audit/inspection readiness.
Executing sponsored studies for assigned areas of focus through all study phases (planning, start-up, conduct, and close-out).
Overseeing projects to ensure completion on-time, within scope, and budget; tracking project performance to analyze the completion of short and long-term goals.
Building and maintaining strong, collaborative relationships with cross-functional leaders, key internal and external stakeholders, and other alliance partners, including CROs.
Collaborating across Clinical Operations and other functions to develop and implementing best practices across Clinical Operations.

Requirements

Experience with Companion Diagnostic (CDx) studies.
Team-oriented with excellent collaboration skills with a cross-functional team.
Open-minded to learn new ways of doing things while leveraging previous experience.
Knowledge of or experience with EU In Vitro Device Regulation (IVDR) submission process
Minimum of a bachelor’s degree in Life Science and/or relevant expertise in the Healthcare Industry or a related field, at least 5years of prior relevant experience including > 1 year’s project management experience.
Conceptual and practical knowledge of Product Development and basic knowledge of Clinical Operations or related areas.

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.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

clinical study manager jobs in north carolina

Clinical Project Manager- IVD

RWE Clinical Project Manager (FSP)

Manager, Site Contracts with Clinical Trials experience Hybrid or Remote in USA-NC

Clinical Project Manager, Immuno-Oncology - IQVIA Biotech

Associate Clinical Project Manager, Immuno-Oncology, Cell and Gene Therapy, IQVIA Biotech

Clinical Sr Project Manager / Assoc Director (Global role, Multisponsor) Remote US & Canada

Associate Clinical Lead Director

Manager Clinical Research

Senior Clinical Project Manager, Immuno-Oncology, IQVIA Biotech

Senior Global Clinical Study Manager

Study Start-up and Regulatory Manager

Clinical Trial Manager - Full Service

Clinical Trial Manager - Full Service

Clinical Trial Manager - CAR T or Ophthalmology

Study Manager - Vaccine

Clinical Study Design Manager

Lead Data Manager

Study Manager - Ophthalmology

Clinical Project Manager - Oncology (Client Dedicated/Remote)

Senior Clinical Project Manager- CNS

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