Hybrid Clinical Research Technician — Drive Impactful Trials

Gamma Phi Omega International; Ann Arbor (MI); Hybrid; USD 45,000 - 65,000; Full time

Benefits offered by this job

Excellent medical, dental and vision

2:1 retirement match

Job summary

University of Michigan in Ann Arbor is seeking a Clinical Research Technician to support study management, regulatory coordination, and data entry. The role will involve performing study procedures with supervision, preparing for visits and audits, and contributing to documentation and training activities.

The position requires an Associate degree in Health Science or related education and 1+ year of clinical research experience, with advanced degrees considered.

Qualifications

• Associate degree in Health Science or equivalent.
• Minimum 1 year of directly related experience in clinical research and clinical trials.
• An advanced degree in a health-related area such as Health Sciences, Behavioral Sciences, Public Health, Health Care Administration, Clinical Research Administration, Social Work, Psychology, Epidemiology, or related field.
• Minimum 3 years of human subject experience (clinical, lab or health regulations) such as patient care, community health and wellness, clinical information, and research.

Responsibilities

• Performs non-GCP related study management activities; performs study procedures with minimal supervision.
• Schedules, assists with preparation for, and attends study initiation meetings, monitor visits, and audits.
• Form completion and reporting to external governing bodies such as the FDA; documenting subject safety and related reporting.
• Enters data to complete forms and supports training (PEERRS, HIPAA, CITI GCP).
• Creates documentation materials for studies.

Education

Associate degree in Health Science

Advanced degree in health-related area

Bachelor's degree in Health Science

Job description

University of Michigan in Ann Arbor is seeking a Clinical Research Technician to support study management, regulatory coordination, and data entry. The role will involve performing study procedures with supervision, preparing for visits and audits, and contributing to documentation and training activities.

The position requires an Associate degree in Health Science or related education and 1+ year of clinical research experience, with advanced degrees considered.