Clinical Study Coordinator
Company: Lumos Clinical Research Center
- Location: San Jose, United States
- Work mode: On-site
- Employment type: Full-time
- Posted: Yesterday
- Offer language: English
Job description
We are seeking an experienced Clinical Study Coordinator to join our growing team and work closely with the Principal Investigator on clinical trials. This role involves coordinating all aspects of study operations, including participant recruitment, data management, regulatory documentation, and study visit coordination.
Key Responsibilities
- Collaborate with the Principal Investigator to ensure smooth study execution in compliance with protocols and regulations.
- Recruit and screen participants for clinical trials.
- Perform and document study procedures, including phlebotomy.
- Manage study data and maintain accurate regulatory and source documentation.
- Administer and score various psychological rating scales (training can be provided if needed).
Qualifications
- Prior experience as a Clinical Research Coordinator required.
- Strong attention to detail and excellent interpersonal communication skills.
- Highly motivated, organized, and able to work independently.
- Proficiency in written and spoken English.
- Phlebotomy skills required (impeccable technique).
- Mental health research experience preferred.
- Experience as a rater for psychometric scales preferred.
Compensation & Benefits
- Competitive, market-based pay, flexible for the right candidate.
- High-growth opportunity in a collaborative, mission-driven environment.
- Position of trust with potential for long-term career advancement.
If you are passionate about advancing clinical research and meet the qualifications above, we’d love to hear from you.
Job Type: Full-time
Pay: $39,009.00 - $100,000.00 per year
Benefits:
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Work Location: In person
