Arch Clinical Trials specializes in psychiatric phase I thru IV clinical trials. We’re looking for a dedicated clinical research coordinator with integrity and a passion for advancing medicine through research.
Job Summary:
The Clinical Research Coordinator (CRC) is primarily responsible for coordinating all clinical research activities per study protocol with moderate supervision. Patient facing vs. data administrative responsibilities will vary per day. The CRC will be responsible for multiple research studies simultaneously, acting as a liaison with the sponsoring agency, community and study participants.
Responsibilities:
- Conducts study start-up activities and prepares and maintains all regulatory documents.
- Prepares study related documentation (case report forms and/or source document templates).
- Identifies and recruits eligible study subjects; conducts informed consent.
- Arranges and conducts clinical research visits.
- Performs clinical and study procedures per protocol, Good Clinical Practice (GCP) guidelines, regulations, and SOPs.
- Maintains all study documents (regulatory binders, source documents, correspondence, etc.).
- Prepares lab kits and requisitions prior to visits.
- Completes basic clinical procedures such as obtaining blood pressure and performing ECGs.
- Collects specimens from subjects and processes specimens to ensure samples are processed/sent out correctly
- Records patient information on source documents and/or electronic web based systems.
- Coordinates reimbursement of subjects
- Attends investigator meetings.
Required Qualifications:
- Excellent communication, problem solving and multitasking skills.
- Bachelor’s or Master's degree in Clinical Research, Nursing, Science, Psychology or related field.
- 5 years experience with Microsoft Office/Google Docs.
- Skill/knowledge in medical terminology.
- Prior working experience in clinical research.
- Strong organizational and computer skills.
Preferred Qualifications:
- 3 or more years of experience as a clinical research coordinator managing multiple study protocols.
- Psychiatric research experience preferred.
- Skill/knowledge in specimen processing/handling.
- Phlebotomy experience is a plus.
- Knowledge of research regulations (FDA, OHRP, GCP, etc.) preferred.
- Familiarity and experience with FDA and IRB regulatory requirements preferred.
Job Type: Full-time
Pay: $52,000.00 - $85,000.00 per year
Benefits:
- 401(k) matching
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Application Question(s):
- Are you located in St. Louis, MO?
Experience:
- Psychiatric clinical trials: 2 years (Preferred)
Ability to Commute:
- St. Louis, MO 63141 (Preferred)
Work Location: In person
