Clinical Research Coordinator
We are a seasoned, growth oriented clinical research company looking to expand our team. Our work environment is very unique and every team member feels valuable and is an integral part of our success and growth.
- PLEASE NOTE: This position is only open to experienced Clinical Research Coordinators, nursing degree preferred but not required. You must have at least 2 years of experience and be a competent Clinical Research Coordinator.
JOB SUMMARY OF RESPONSIBILITY
Coordination of clinical trials to include:
- Obtaining Informed Consent under the direction of the Principal Investigator
- Collecting, maintaining and organizing study data per each protocol’s requirements
- Investigational Product accountability per each protocol’s requirements
- Identification, documentation and reporting of Adverse Events (AEs) and Serious Adverse Events (SAEs) under the direction of the PI
- Completion of Case Report Forms (CRFs)
- Coordination processing, shipping and specimen collection for clinical trials.
- Good Clinical and Phlebotomy skills
- Organization and preparation of data for monitoring.
- Competently Conduct all aspects of the clinical research subject visits
QUALIFICATIONS :
- Good Character
- Love for people and clinical research
- Medical degree - Nursing degree preferred
- Knowledge of FDA Regulations and HIPAA Rules
- Knowledge of Good Clinical Practice
- Proficiency in Microsoft Office
- Excellent written and oral skills
- High attention to detail and organization
Job Type: Full-time
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Education:
Experience:
- Clinical Research: 2 years (Required)
License/Certification:
- Nursing License (Preferred)
Ability to Relocate:
- Chesterfield, MO 63017: Relocate before starting work (Required)
Work Location: In person
