Proclinical Staffing
Unblinded Clinical Research Coordinator - Edmond, OK
Proclinical Staffing, Edmond, Oklahoma, United States, 73034
Unblinded Clinical Research Coordinator - Edmond, OK
Direct message the job poster from Proclinical Staffing
Unblinded Clinical Research Coordinator – Contract – Edmond, OK
Looking to uncover insights that could revolutionize the future of medicine and drive breakthroughs in patient 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 while maintaining the integrity of blinded and unblinded roles. This position requires strong organizational skills, attention to detail, and the ability to work collaboratively with site managers, study participants, and sponsors.
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 collaboratively as part of a team.
Excellent organizational and problem‑solving skills.
Local travel may be required for multi‑site locations.
Responsibilities will include:
Communicate study procedures and expectations to participants or caregivers.
Monitor study activities to ensure adherence to 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 restocking is needed.
Perform protocol‑specific procedures such as vital signs, electrocardiograms, and specimen collection.
Record and report adverse events and side effects, collaborating with investigators for sponsor reporting.
Resolve EDC queries within 24 hours of issuance.
Dispense and manage investigational products, including logging shipments, dispensing to subjects, and maintaining accurate accountability records.
Prepare and maintain master logs for each study, including informed consent forms and patient enrollment.
Participate in quality assurance audits and ensure proper labeling and organization of drug storage areas.
Maintain accurate temperature logs for IP storage equipment.
Train backup team members and ensure all required IP documents and equipment are available for study conduct.
Communicate with sponsors regarding IP management and attend investigator meetings and site initiation visits.
For questions, please contact
Jackie Cerchio
at
j.cerchio@proclinical.com
To apply, click “Apply” or request a callback 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.
By submitting this application, you confirm that you’ve read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.proclinical.com/privacy-policy
#J-18808-Ljbffr
Unblinded Clinical Research Coordinator – Contract – Edmond, OK
Looking to uncover insights that could revolutionize the future of medicine and drive breakthroughs in patient 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 while maintaining the integrity of blinded and unblinded roles. This position requires strong organizational skills, attention to detail, and the ability to work collaboratively with site managers, study participants, and sponsors.
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 collaboratively as part of a team.
Excellent organizational and problem‑solving skills.
Local travel may be required for multi‑site locations.
Responsibilities will include:
Communicate study procedures and expectations to participants or caregivers.
Monitor study activities to ensure adherence to 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 restocking is needed.
Perform protocol‑specific procedures such as vital signs, electrocardiograms, and specimen collection.
Record and report adverse events and side effects, collaborating with investigators for sponsor reporting.
Resolve EDC queries within 24 hours of issuance.
Dispense and manage investigational products, including logging shipments, dispensing to subjects, and maintaining accurate accountability records.
Prepare and maintain master logs for each study, including informed consent forms and patient enrollment.
Participate in quality assurance audits and ensure proper labeling and organization of drug storage areas.
Maintain accurate temperature logs for IP storage equipment.
Train backup team members and ensure all required IP documents and equipment are available for study conduct.
Communicate with sponsors regarding IP management and attend investigator meetings and site initiation visits.
For questions, please contact
Jackie Cerchio
at
j.cerchio@proclinical.com
To apply, click “Apply” or request a callback 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.
By submitting this application, you confirm that you’ve read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.proclinical.com/privacy-policy
#J-18808-Ljbffr