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Clinical Research Coordinator
Headlands Research, Inc.
Plymouth
On-site
GBP 60,000 - 80,000
Full time
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Job summary
An established industry player in clinical trials is seeking a Clinical Research Coordinator in Plymouth. This role involves managing clinical research protocols, ensuring compliance with ICH GCP guidelines, and fostering participant engagement. You will work closely with investigators and staff to recruit and screen study subjects, collect data, and manage study activities. Join a forward-thinking company that values innovation and quality in clinical trial delivery, contributing significantly to the advancement of medical research. If you have a passion for clinical research and a commitment to excellence, this opportunity is perfect for you.
Qualifications
- Experience in conducting clinical trials with knowledge of ICH GCP.
- Excellent interpersonal and communication skills for effective interaction.
Responsibilities
- Manage clinical research protocols and ensure compliance with ICH GCP.
- Recruit and screen study subjects, collect and record data accurately.
- Train ancillary staff and manage investigational products.
Skills
Education
Tools
Job description
At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. We’re an exceptional family of next-generation clinical trial sites, integrating cutting edge technology and high-quality support services, and significantly expanding participant engagement Founded in 2018, our company operates 20+ clinical trial sites in the US and Canada with rapid plans for expansion.
The Role
Headlands Research in Plymouth is looking for a Clinical Research Coordinator to manage clinical research protocols. This individual will work directly with the investigators, and other research staff to ensure protocol visits are being conducted according to ICH GCP guidelines.
- Comprehend study design of each protocol that is assigned
- Perform procedures in compliance with the study protocol
- Recruit and screen study subjects according to specific protocol requirements
- Collect and record study data in source documents via electronic system (CRIO)
- Manage study related activities
- Adherence to protocol requirements
- Review laboratory data
- Assess and document compliance
- Manage investigational product
- Assess, record, and report Adverse Events as outlined in the protocol
- Manage/train ancillary staff
Education:
- Experience and training in conducting clinical trials with knowledge of ICH GCP
OR
- Two years of college in a health-related program or LPN
OR
- Bachelor’s degree in a health or scientific related program
- A thorough understanding of regulatory requirements
- Excellent interpersonal and communication skills: Able to interact effectively with professional, administrative staff, sponsor and regulatory representatives, patients, potential subjects, and referral sources.
- Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens
- Experience with CRIO (Clinical Trial Management System) is a plus
- Experience with administering vaccines is a plus
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