What are the responsibilities and job description for the Unblinded Clinical Research Coordinator - Fort Collins, CO position at Proclinical Staffing?
Unblinded Clinical Research Coordinator - Contract - Fort Collins, CO
Ready to be the heartbeat of medical research? Join our client and assist in turning innovative science into life-changing care!
Proclinical is seeking an Unblinded Clinical Research Coordinator to support the daily operations of clinical trials.
Primary Responsibilities:
In this role, you will focus on managing Investigational Product (IP) for clinical research studies, ensuring compliance with protocols and maintaining the integrity of blinded and unblinded staff roles. This position requires strong organizational skills, attention to detail, and the ability to work both independently and collaboratively.
Skills & Requirements:
- Experience in clinical research is preferred.
- High school diploma or GED required; some college coursework is preferred.
- Strong ability to work independently and as part of a team.
- Excellent organizational and communication skills.
- Local travel may be required for multi-site locations.
The Clinical Research Coordinator's responsibilities will be:
- Communicate study procedures and outcomes to participants or caregivers.
- Monitor study activities to ensure compliance with protocols and regulatory requirements.
- Complete and maintain accurate source documentation during patient visits and enter data into the electronic data capture (EDC) system within 48 hours.
- Manage inventory of lab and study supplies, notifying the manager when replenishment is needed.
- Perform protocol-specific procedures such as interviews, vital signs, electrocardiograms, and laboratory specimen collection.
- Record adverse events and side effects, and collaborate with investigators for reporting.
- Resolve electronic data queries within 24 hours of issuance.
- Dispense medical devices or drugs, calculate dosages, and provide necessary instructions.
- Log and manage drug accountability, including receipt, storage, dispensing, and return of investigational products.
- Maintain accurate master logs for each study, including informed consent forms, patient IDs, and enrollment records.
- Participate in quality assurance audits.
- Organize and label drug storage areas, ensuring proper temperature monitoring and logging.
- Prepare the site for study conduct, including training backup team members and attending investigator meetings and site initiation visits.
- Communicate with sponsors regarding IP management and ensure all required documents and equipment are obtained.
- Administer investigational products as per protocol and maintain accurate IP accountability records.
- Collaborate with unblinded monitors and participate in unblinded monitor visits.
Compensation:
- $20 to $27 per hour
If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at j.cerchio@proclinical.com
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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Salary : $20 - $27
