Assistant Clinical Research Coordinator

Om Research LLC; Camarillo (CA); On-site; USD 45,000 - 75,000; Full time

Job summary

Join a dynamic research team as an Assistant Clinical Research Coordinator, where you'll play a vital role in conducting studies in compliance with federal regulations. This position involves preparing for study initiation, recruiting and screening subjects, and ensuring accurate documentation of study procedures. Your contributions will help advance medical research and improve patient outcomes. If you have a passion for clinical research and a keen attention to detail, this is an exciting opportunity to make a meaningful impact in the field. Embrace the chance to work in a collaborative environment that values your expertise and dedication.

Qualifications

• Experience in clinical research coordination and subject recruitment is essential.
• Knowledge of federal regulations and study protocols is crucial.

Responsibilities

• Prepare for study initiation and obtain necessary physician signatures.
• Recruit, screen, and schedule subjects while maintaining study files.

Skills

Clinical Research Coordination

Subject Recruitment

Phlebotomy

Spanish Language

Job description

The Assistant Clinical Research Coordinator comprises an integral part of the research team. Working under the PI, he/she is responsible for conducting the study in accordance with federal regulations. Some responsibilities of the Assistant Clinical Research Coordinator include:

1. Preparing for study initiation
2. Obtaining physician signatures
3. Recruiting subjects
4. Screening and scheduling subjects
5. Getting voluntary subject consent
6. Training subjects on protocol expectations
7. Performing study/protocol procedures in a detailed and accurate manner
8. Maintaining study files
9. Tracking subjects, avoiding lost-to-follow-up's
10. Documenting an adverse event
11. Processing and shipping lab work
12. Maintaining communication and correspondence (by telephone, email, fax, etc.) with subjects, sponsor, monitor and other site study personnel
13. Completing case report forms (CRF's) for PI review and approval
14. Helping study monitors with CRA corrections
15. Maintaining study-specific supplies
16. Preparing for study closure and archiving

Knowledge of Spanish and/or Phlebotomy training will be an added advantage.