Durham, NC · On-site
$93K - $232K/yr
... 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 ...
Durham, NC · On-site
$93K - $232K/yr
... 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 ...
Durham, NC · On-site
$93K - $232K/yr
... 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 ...
Durham, NC · On-site
$93K - $232K/yr
... 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 ...
Durham, NC · On-site
$93K - $232K/yr
... 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 ...
Durham, NC · On-site
$93K - $232K/yr
... 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 ...
CANDIDATE MUST BE CERTIFIED IN AT LEAST ONE CLINICAL APPLICATION The North Carolina Department of Health and Human Services requires the services of an EXPERT Epic Clinical project manager to manage ...
CANDIDATE MUST BE CERTIFIED IN AT LEAST ONE CLINICAL APPLICATION The North Carolina Department of Health and Human Services requires the services of an EXPERT Epic Clinical project manager to manage ...
Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads run their own studies.
Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads run their own studies.
Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads run their own studies.
Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads run their own studies.
Morrisville, NC · On-site
Clinical Project Manager II - Early Phase Virology /Healthy Volunteer Studies (Sponsor Dedicated - US Remote; Preference for Hybrid Foster City, CA) Syneos Health is a leading fully-integrated life ...
Morrisville, NC · On-site
Clinical Project Manager II - Early Phase Virology /Healthy Volunteer Studies (Sponsor Dedicated - US Remote; Preference for Hybrid Foster City, CA) Syneos Health is a leading fully-integrated life ...
Durham, NC · On-site
$93K - $232K/yr
In this role, the clinical project manager will be responsible for end-to-end project delivery of real-world observational studies within the oncology therapeutic area. It is important for this ...
Durham, NC · On-site
$93K - $232K/yr
In this role, the clinical project manager will be responsible for end-to-end project delivery of real-world observational studies within the oncology therapeutic area. It is important for this ...
Durham, NC · On-site
$93K - $232K/yr
In this role, the clinical project manager will be responsible for end-to-end project delivery of real-world observational studies within the oncology therapeutic area. It is important for this ...
Durham, NC · On-site
$93K - $232K/yr
In this role, the clinical project manager will be responsible for end-to-end project delivery of real-world observational studies within the oncology therapeutic area. It is important for this ...
$51K - $127K/yr
IQVIA is looking for a Clinical Project Coordinator to join our growing team. Role can be homebased ... Manage study specific eTraining and oversee compliance. Support the updating and maintenance of ...
New
$51K - $127K/yr
IQVIA is looking for a Clinical Project Coordinator to join our growing team. Role can be homebased ... Manage study specific eTraining and oversee compliance. Support the updating and maintenance of ...
New
The Clinical Project Manager at WEP Clinical is responsible for the setup, implementation, and management of clinical trials, ensuring patient safety, data integrity, and high-quality delivery in ...
The Clinical Project Manager at WEP Clinical is responsible for the setup, implementation, and management of clinical trials, ensuring patient safety, data integrity, and high-quality delivery in ...
Durham, NC · On-site
$93K - $232K/yr
We are seeking a US-based Senior Clinical Project Manager with proven experience in Central Nervous System (CNS) clinical trials to join IQVIA Biotech. This role is ideal for a seasoned project ...
Durham, NC · On-site
$93K - $232K/yr
We are seeking a US-based Senior Clinical Project Manager with proven experience in Central Nervous System (CNS) clinical trials to join IQVIA Biotech. This role is ideal for a seasoned project ...
Durham, NC · On-site
$93K - $232K/yr
Overview As a Clinical Project Manager, you'll play an essential role in accelerating clinical trial delivery and improving patient lives by helping bring new therapies to market faster. You will ...
Durham, NC · On-site
$93K - $232K/yr
Overview As a Clinical Project Manager, you'll play an essential role in accelerating clinical trial delivery and improving patient lives by helping bring new therapies to market faster. You will ...
$51K - $127K/yr
IQVIA is looking for a Clinical Project Coordinator to join our growing team. Role can be homebased ... Manage study specific eTraining and oversee compliance. Support the updating and maintenance of ...
New
$51K - $127K/yr
IQVIA is looking for a Clinical Project Coordinator to join our growing team. Role can be homebased ... Manage study specific eTraining and oversee compliance. Support the updating and maintenance of ...
New
Durham, NC · On-site
$51K - $127K/yr
Support, with minimal supervision, the Project Leader (PL) and Clinical Project Manager (CPM) with project management activities to ensure all work is conducted in accordance with standard operating ...
New
Durham, NC · On-site
$51K - $127K/yr
Support, with minimal supervision, the Project Leader (PL) and Clinical Project Manager (CPM) with project management activities to ensure all work is conducted in accordance with standard operating ...
New
Durham, NC · On-site
$93K - $232K/yr
Overview As a Clinical Project Manager, you'll play an essential role in accelerating clinical trial delivery and improving patient lives by helping bring new therapies to market faster. You will ...
Durham, NC · On-site
$93K - $232K/yr
Overview As a Clinical Project Manager, you'll play an essential role in accelerating clinical trial delivery and improving patient lives by helping bring new therapies to market faster. You will ...
Durham, NC · On-site +1
Our Phase I team is seeking a Sr. Clinical Project Manager to join our growing team. This role requires 4-5 + years of global project management experience , with mandatory experience in phase I
Durham, NC · On-site +1
Our Phase I team is seeking a Sr. Clinical Project Manager to join our growing team. This role requires 4-5 + years of global project management experience , with mandatory experience in phase I
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... The Project Management team is engaged in all aspects of the trial collaborating with scientific ...
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... The Project Management team is engaged in all aspects of the trial collaborating with scientific ...
Durham, NC · On-site +1
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... What the Project Management department does at Worldwide Worldwide Clinical Trials Project ...
Durham, NC · On-site +1
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... What the Project Management department does at Worldwide Worldwide Clinical Trials Project ...
Our FSO team is seeking an Oncology Sr. Clinical Project Manager or Project Manager II to join our growing team. This role requires 3-5 + years of global project management experience , with ...
Our FSO team is seeking an Oncology Sr. Clinical Project Manager or Project Manager II to join our growing team. This role requires 3-5 + years of global project management experience , with ...
$28.27 - $35.28
16% of jobs
$40.70 is the 25th percentile. Wages below this are outliers.
$35.28 - $42.29
12% of jobs
$42.29 - $49.31
14% of jobs
The median wage is $53.98 / hr.
$49.31 - $56.32
13% of jobs
$56.32 - $63.33
15% of jobs
$66.54 is the 75th percentile. Wages above this are outliers.
$63.33 - $70.34
13% of jobs
$70.34 - $77.35
4% of jobs
$77.35 - $84.36
5% of jobs
$84.36 - $91.37
5% of jobs
$91.37 - $98.38
1% of jobs
$98.38 - $105.39
2% of jobs
$28
$59
$105
A Freelance Clinical Project Manager oversees clinical trials and research projects on a contractual basis. They ensure studies comply with regulations, manage timelines and budgets, coordinate teams, and communicate with stakeholders. Unlike full-time employees, they work independently and may juggle multiple projects from different sponsors or CROs. Their expertise helps companies efficiently execute clinical trials while maintaining flexibility in staffing.
A Freelance Clinical Project Manager requires expertise in clinical trial management, regulatory compliance, protocol development, and budgeting, often supported by a science degree and several years of experience in clinical research. Familiarity with tools like clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as PMP or GCP are highly valued. Outstanding organization, problem-solving, and interpersonal skills help them coordinate diverse teams and manage multiple projects simultaneously. These skills are crucial for ensuring trials are completed on time, within budget, and in accordance with industry regulations.
Freelance clinical project managers often encounter challenges such as coordinating across geographically dispersed teams, adapting to varying sponsor requirements, and ensuring timely regulatory submissions. You can prepare by staying updated on industry best practices, strengthening your project management and communication skills, and building familiarity with multiple clinical trial management platforms. Successfully navigating these challenges relies on proactive planning, flexibility, and establishing clear communication channels with all stakeholders. Many freelancers also build strong professional networks to access additional support and resources when needed.
8.1
Based on 53 frontline employees who took The Breakroom Quiz
62nd of 223 rated it services
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 athttps://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.
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At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.
Health care and social assistance
10,000+ Employees
Durham, NC, US
