Clinical Research Coordinator
No Resistance Consulting Group
About the Role
No Resistance is seeking motivated individuals to join our team as a Clinical Research Coordinator. In this role, you will play a pivotal part in the implementation and execution of clinical research projects, ensuring the successful attainment of quality, safety, regulatory, and financial objectives.
Key Responsibilities
- Maintaining regulatory binders, inventory of study-specific and clinical supplies.
- Recruiting and enrolling study subjects.
- Obtaining informed consent.
- Collecting nasal swab samples.
- Testing samples on investigational laboratory PCR analyzers.
- Data collection and entry.
- Query resolution.
- Assuring protocol compliance and efficient workflow including organizing clinical work areas, tracking and ordering study supplies and shipping materials, checking and replacing expired items.
Key Success Factors
- Ability to work independently.
- Desire to work in a clinical environment with direct patient contact.
- Genuine interest in research.
- Timely in all communications.
- Superior attention to detail.
Requirements & Tech Stack
- No clinical trial experience is required. No Resistance will train the right candidate(s).
- Experience with PCR analyzers is a plus.
Qualifications
- While not a requirement, senior pre-medical students who hope to gain experience in clinical research or recent graduates who have a "gap" year before they start medical school are encouraged to apply.
Job Details
- Job Location: Point Loma, CA
- Job Type: Full-time
- Pay: $22.50-$25.00 per hour
- Expected Hours: 40 per week
- Schedule: Monday to Friday, 8:30 am to 5:00 pm (no weekend requirements)
- Work Location: In person
Benefits
- 401(k)
- Dental Insurance
- Health Insurance
- Paid time off
- Vision Insurance