Proclinical Staffing
Unblinded Clinical Research Coordinator
Proclinical Staffing, Fort Collins, Colorado, us, 80523
Unblinded Clinical Research Coordinator - Contract - Fort Collins, CO
Proclinical is seeking an Unblinded Clinical Research Coordinator to support the daily operations of assigned clinical trials in Fort Collins, CO.
Primary Responsibilities The successful candidate will play a key part in managing investigational products (IP) and ensuring compliance with study protocols and regulatory requirements. This position requires strong organizational skills, attention to detail, and the ability to work both independently and collaboratively.
Communicate with site managers and study participants regarding study‑related information.
Adhere to site Standard Operating Procedures (SOPs) and maintain the blind for applicable studies.
Manage all aspects of investigational product (IP), including receipt, storage, dispensing, destruction, return, and administration.
Maintain accurate IP accountability and ensure proper documentation in logs and binders.
Monitor study activities to ensure compliance with protocols and regulatory requirements.
Complete and enter source documentation into the electronic data capture (EDC) system within 48 hours of patient visits.
Perform protocol‑specific procedures such as interviewing subjects, taking vital signs, performing electrocardiograms, and collecting laboratory specimens.
Record and report adverse events and side effects, resolving queries within 24 hours.
Inventory lab and study supplies, notifying the manager when supplies need replenishment.
Prepare the site for study conduct, including attending investigator meetings and site initiation visits.
Train backup unblinded or pharmacy team members as needed.
Communicate with sponsors regarding IP management and ensure all required documents and equipment are available.
Participate in quality assurance audits and maintain accurate temperature logs for IP storage.
Skills & Requirements
Experience in clinical research is preferred.
Ability to work independently and collaboratively as part of a team.
High school diploma or GED required; some college education preferred.
Strong organizational and problem‑solving skills.
Local travel may be required for multi‑site locations.
For questions, contact
Jackie Cerchio
at
j.cerchio@proclinical.com .
If you are interested in applying, please click ‘Apply’ or request a call back at the top of the page.
#J-18808-Ljbffr
Primary Responsibilities The successful candidate will play a key part in managing investigational products (IP) and ensuring compliance with study protocols and regulatory requirements. This position requires strong organizational skills, attention to detail, and the ability to work both independently and collaboratively.
Communicate with site managers and study participants regarding study‑related information.
Adhere to site Standard Operating Procedures (SOPs) and maintain the blind for applicable studies.
Manage all aspects of investigational product (IP), including receipt, storage, dispensing, destruction, return, and administration.
Maintain accurate IP accountability and ensure proper documentation in logs and binders.
Monitor study activities to ensure compliance with protocols and regulatory requirements.
Complete and enter source documentation into the electronic data capture (EDC) system within 48 hours of patient visits.
Perform protocol‑specific procedures such as interviewing subjects, taking vital signs, performing electrocardiograms, and collecting laboratory specimens.
Record and report adverse events and side effects, resolving queries within 24 hours.
Inventory lab and study supplies, notifying the manager when supplies need replenishment.
Prepare the site for study conduct, including attending investigator meetings and site initiation visits.
Train backup unblinded or pharmacy team members as needed.
Communicate with sponsors regarding IP management and ensure all required documents and equipment are available.
Participate in quality assurance audits and maintain accurate temperature logs for IP storage.
Skills & Requirements
Experience in clinical research is preferred.
Ability to work independently and collaboratively as part of a team.
High school diploma or GED required; some college education preferred.
Strong organizational and problem‑solving skills.
Local travel may be required for multi‑site locations.
For questions, contact
Jackie Cerchio
at
j.cerchio@proclinical.com .
If you are interested in applying, please click ‘Apply’ or request a call back at the top of the page.
#J-18808-Ljbffr