Senior Clinical Research Associate - Contract Position
HealthcareClinical Researcher
1 views0 saves0 applied
Quick Summary
Overview
This position is listed on behalf of a partner company, who manages all applications and next steps.
Technical Tools
HealthcareClinical Researcher
This contract opportunity is designed for an experienced clinical research professional who wants to play a key role in the successful execution of clinical trials. You will monitor studies involving investigational and approved products while ensuring compliance with protocols, SOPs, ICH GCP, and applicable regulatory requirements. The role covers the full site lifecycle, from qualification and initiation through interim monitoring and close-out activities. You will work closely with investigators, coordinators, study teams, and other stakeholders to maintain data quality, resolve issues, and support trial progress. The position also offers an opportunity to mentor less experienced CRAs and contribute practical solutions to complex study challenges. Frequent travel is an important component of the role, with travel requirements of up to 65%.
- Conduct qualification, initiation, interim, and close-out site visits for clinical studies involving investigational and approved products.
- Monitor clinical trials to ensure studies are conducted, documented, and reported in accordance with protocols, SOPs, ICH GCP, and applicable regulatory requirements.
- Train and support site personnel on therapeutic areas, protocol requirements, source documentation, and case report form completion.
- Manage and track investigational supplies, including preparation, shipment, dispensing, inventory, reconciliation, and return.
- Monitor laboratory sample storage and shipment activities and ensure appropriate documentation.
- Track and report site enrollment and termination updates, monitoring activities, protocol deviations, serious adverse events, and laboratory abnormalities.
- Review source data and case report forms for accuracy, completeness, consistency, and data integrity, identifying and resolving ongoing issues.
- Review data queries and listings and collaborate with study sites to resolve discrepancies efficiently.
- Review regulatory documentation for accuracy and completeness and provide support when sites encounter regulatory issues.
- Maintain complete and accurate study files and conduct regular reviews to ensure required documentation is present.
- Maintain consistent and timely communication with investigators, coordinators, study centers, project teams, and other clinical trial stakeholders.
- Serve as a resource to project team members and provide guidance and practical solutions to CRA I and CRA II colleagues.
Requirements
~1 min read- RN, bachelor's degree, or advanced degree in biological sciences or a related field, or an equivalent combination of relevant education, training, and experience.
- Previous CRA experience demonstrating progressive career growth and increasing responsibility within clinical research.
- Strong knowledge of clinical trial monitoring practices and the medical and pharmaceutical industries, including relevant terminology and processes.
- Extensive knowledge of FDA regulations and their practical application in clinical research.
- Strong understanding of protocol compliance, ICH GCP, SOPs, data integrity, and regulatory documentation.
- Excellent attention to detail with strong organizational, interpersonal, communication, and problem-solving skills.
- Ability to manage multiple priorities efficiently and adapt to changing study requirements.
- Strong ability to identify issues, investigate discrepancies, and develop practical solutions.
- Ability to build effective working relationships with investigators, site personnel, clients, and cross-functional project teams.
- Willingness and ability to travel by air or car on short notice, with travel requirements of up to 65%.
- Proficiency in Microsoft Word, Excel, and PowerPoint.
What We Offer
~2 min read✓Contract position with the opportunity to contribute to clinical research supporting innovative treatments and healthcare solutions.
✓Opportunity to work across pharmaceutical, biotechnology, and medical device clinical research environments.
✓Collaborative environment focused on clinical research quality, integrity, and professional excellence.
✓Opportunity to work with experienced clinical research professionals and multidisciplinary study teams.
✓Exposure to a broad range of clinical trial monitoring and site management activities.
✓Opportunity to support and mentor less experienced clinical research associates.
✓Meaningful contribution to the successful execution of studies and the advancement of global health.
Location & Eligibility
Where is the job
United States
Remote within one country
Who can apply
US
Listing Details
- Posted
- October 2, 2026
- First seen
- October 2, 2026
- Last seen
- October 2, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 68%
- Scored at
- October 2, 2026
Signal breakdown
freshnesssource trustcontent trustemployer trust
External application
Similar Clinical Researcher jobs
View all →Remote
Clinical Trial Manager - FSP
Full-timeRemote
Sr Clinical Research Associate Contractor (France)
Part-time
Clinical Research Coordinator- Phase II-III - Full-Time - Wolf River - Registered Nurse (RN) Preferred
UNIV - Clinical Research Coordinator - Department of Medicine: Division of Pulmonary
Remote
Senior Clinical Research Associate - Contract Position
ContractRemote
Remote
Senior Clinical Research Associate
USD 130000–155000
Full TimeRemote
Newsletter
Stay ahead of the market
Get the latest job openings, salary trends, and hiring insights delivered to your inbox every week.
A
B
C
D
No spam. Unsubscribe at any time.