Community Health Network
Clinical Research Coordinator
How your CV stacks up
Upload your CV to see how well it fits this job role
?%
Join Community
Community Health Network has an excellent opportunity available within our clinical research department. If you are looking for challenging work and meaningful advancement, then you should consider a career with Community.
Make a Difference
The Clinical Research Coordinator will be responsible for assessing, planning, implementing, and executing clinical research protocols in conjunction with the Principal Investigator and clinical research team.
Your Exceptional Qualifications
Research Coordinator Duties:
- Identifies and screens appropriate candidates for eligibility for research studies.
- Obtains informed consent from eligible patients for a research study.
- Maintains an effective data management system to track study participants and activities.
- Collects data and completes case report forms and data queries as specified by the study protocol.
- Prepares source documents for data collection.
- Assists in identifying study related procedures for the project budget.
Administrative Duties:
Reasons to use Rodeo
Start with a chat, not a search bar
Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.
It searches the market for you
Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
- Attends Investigator and Coordinator Meetings as requested by the sponsor along with appropriate department, division and/or service line meetings.
- Assists in determining facility, staff and supply needs required for set-up and implementation of a new study.
- Prepares for and is present for sponsor representative site visits.
- Serves as an educator and resource person for patients, family, staff and physicians.
Laboratory Duties:
- Performs phlebotomy, ECG and other testing, as needed after trained.
- Prepares and processes laboratory specimens for shipment according to study lab manual.
- Reviews labs and ancillary tests; and reports results to Principal Investigator and appropriate personnel in a timely manner.
Interpersonal Skills:
- Effectively problem solves and informs Manager and Principal Investigator when appropriate.
Communication:
- Communicates on a regular basis with the Investigators, Research Team, Hospital Staff, Monitor and other sponsor representatives to ensure adherence to Good Clinical Practice (GCP) guidelines.
Get help with your application
Your very own career expert that helps elevate your application to the next level.
Safety & Compliance:
- Coordinates, implements and completes clinical research studies in accordance with protocol guidelines, GCP, ICH, local, state and federal standards.
- Monitors adherence to protocols, and reports violations in a timely manner to the sponsor and the IRB.
Individuals may not perform all of these duties, or may perform additional, related duties not listed here.
EDUCATION
- 2 year / Associate Degree (Required)
- 4 year / Bachelor's Degree (Preferred)
In lieu of the above education requirements, a combination of experience and education will be considered.
LICENSE & CERTIFICATION REQUIREMENTS
- Certifications/Licensures: (Certified Clinical Research Associate (CCRA - ACRP), Certified Clinical Research Coordinator (CCRC-ACRP), Certified Clinical Research Professional (CCRP-SoCRA)) within three (3) years from hire
EXPERIENCE
- Previous experience in data abstraction is helpful (Preferred)
- Minimum of 2 years in a related field of healthcare (Required)
“It took my CV and asked me questions relevant to understanding what kind of jobs to suggest for me. Suggestions were almost perfect. Jobs were exactly what I’ve been looking for.”
Jessica, London
Skills