Job Description

***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:

• Patient-facing coordination experience.
• Study drug dispensing, pharmacy tech, or compounding experience a plus.
• Strong attention to detail and protocol compliance.

Why Join Us:

• Be a key part of innovative clinical trials impacting patient care.
• Collaborative, mission-driven research environment. xywuqvp
• Opportunities for training and professional growth.

Job Tags

Full time, Contract work

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