Clinical Research Coordinator - 243120

***Seeking a Clinical Research Coordinator in Lakewood, CO to join our clinical trials team***Full Job Description:Position: Clinical Research CoordinatorLocation: Lakewood, COEmployment Type: Full time; Contract to HirePay: Up to 75kPosition 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 experienceo Ophthalmic experience preferred• Experience / Knowledge / Skills:Prior annual review or promotion assessment exceeds expectations and shows highproficiency in the job requirementso Effective oral and written communicationo Delivers safe and appropriate care to patients in addition to the requirements outlined bystudy protocols• Certifications / Training:o ICH GCP Training / Certificateo IATA CertificationDuties:• 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 ensureadequate 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 accuratelyPreferred 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.Opportunities for training and professional growth.