***Seeking a Clinical Research Coordinator in Lakewood, CO to join our clinical trials team***
If you want to know about the requirements for this role, read on for all the relevant information.
Full Job Description:
Position: Clinical Research Coordinator
Location: Lakewood, CO
Employment Type: Full time; Contract to Hire
Pay: Up to 75k
Position Overview:
The research coordinator is primarily responsible for coordinating research patient visits according to both the ICH-GCP guidelines and the IRB-approved study protocol and/or manual of procedures. Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience / knowledge and the needs of the organization which are subject to change from time to time.
Minimum Qualifications:
• Education:
o College degree preferred or significant relevant experience
o Ophthalmic experience preferred
• Experience / Knowledge / Skills:
Prior annual review or promotion assessment exceeds expectations and shows high
proficiency in the job requirements
o Effective oral and written communication
o Delivers safe and appropriate care to patients in addition to the requirements outlined by
study protocols
• Certifications / Training:
o ICH GCP Training / Certificate
o IATA Certification
Duties:
• Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study
• Administer sponsor required questionnaires (i.e. VFQ)
• Works with team member responsible for ordering study supplies (lab kits, shippers, etc.) to ensure
adequate inventory is on hand
• Ensures study staff is properly trained on study-related information (i.e. protocol, ICF, manuals,
etc.) and that the training is documented
• Creates, manages, and maintains source documents for each trial
• Attends teleconferences and Investigator Meetings as requested by research director
• Reviews and comprehends all study protocols, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections
• Works with other members of the study team and clinical team to recruit eligible candidates to meet enrollment goals
• Screens subjects for eligibility using protocol-specific inclusion and exclusion criteria, documenting each potential participant's eligibility accurately
Preferred Experience:
Why Join Us:
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