What are the responsibilities and job description for the Unblinded Clinical Research Coordinator - San Antonio position at Proclinical Staffing?
Unblinded Clinical Research Coordinator - Contract - San Antonio TX
Ready to be the heartbeat of clinical research? Join our client as a Research Coordinator 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 Products (IP) and ensuring compliance with study protocols and regulatory requirements. You will play a key role in maintaining the integrity of blinded studies while overseeing all aspects of IP management. 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 education is preferred.
- Strong organizational and problem-solving skills.
- Ability to work independently and as part of a team.
- Local travel may be required for multi-site locations.
The Research Coordinator's responsibilities will be:
- Communicate with site managers and study participants regarding study procedures and outcomes.
- Ensure compliance with study protocols, local, federal, and state regulations, and institutional policies.
- Complete and maintain accurate source documentation during patient visits and enter data into the electronic data capture (EDC) system within 48 hours.
- Monitor study activities, including adverse event reporting and resolution of queries within 24 hours.
- Manage inventory of lab and study supplies, notifying the manager when replenishment is needed.
- Perform protocol-specific procedures such as vital signs, electrocardiograms, and laboratory specimen collection.
- Dispense and manage investigational products, including logging shipments, maintaining accountability records, and ensuring proper storage conditions.
- Prepare and organize drug storage areas, maintain temperature logs, and ensure compliance with IP manuals.
- Train backup unblinded team members and ensure all required training and documentation for IP management are completed.
- Attend investigator meetings, site initiation visits, and quality assurance audits.
- Collaborate with sponsors and unblinded monitors to address IP-related issues and ensure smooth study operations.
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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