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French Camp, California
Posted: 31-Jan-25
Location: Los Angeles, California
Categories:
Internal Number: 146035744
Join our team as a Clinical Research Coordinator/Manager in the Division of Dermatology, working under the guidance of the Principal Investigator (PI). You’ll manage and coordinate clinical research trials, from recruiting and screening participants to collecting data and ensuring the trials run smoothly.
Your key tasks will include:
- Recruiting and assessing potential study participants.
- Building and maintaining strong relationships with participants to encourage their ongoing involvement.
- Keeping participant information confidential.
- Collecting data and documenting consent and any adverse events.
- Collaborating with the CTSI computational team to identify and recruit patients or collect specimens.
- Assisting with the creation of new research contracts and protocols.
We’re looking for someone who’s detail-oriented and passionate about advancing dermatology research!
Salary:$33.63 - $54.11 hourly- Ability and experience to manage and run multiple clinical studies concurrently.
- Ability to coordinate /prioritize work schedule, subject enrollment and P.I’s time
- Familiarity with federal regulatory standards relating to human subjects research and NIH
- Familiarity with clinical studies protocol development.
- Ability to assess regulatory needs/obligations/hurdles of research protocols.
- Experience in IRB applications and informed consent.
- Ability to communicate well with scientific collaborators and laboratory personnel.
- Skills in writing both for lay and scientific audience (methods sections of papers/ads/newsletter)
- Appreciation of the needs to enroll and close studies on schedule
- Ability to organize and present data in spreadsheets.
- Understand spreadsheets and needs of statistical analyst.
- Experience developing quality management systems for complex research studies.
- Knowledge of staff certification requirements for clinical trials (human subjects training, laboratory, radiation and biohazard safety, IATA shipping, etc).
- Experience in developing SOPs, SSPs, CRFs and study regulatory files.
