Clinical Research Coordinator

• This is a temporary to permanent Clinical Research position.
• This position has the possibility to be hybrid if preferred.
• This position is full time in Santa Monica. Ideal candidate will live in Santa Monica because the commute is substantial otherwise.
• Rate if hired on permanently: around TBD-TBD per hour. Candidate must be aware of this before accepting contract.

Clinical Research Coordinator

• Certs: CCRC (ACRP) preferred, Must have Blood Draw Cert. Meaning must be a phlebotomist, MA, LVN, or RN
• Schedule: 5x8's Days, Hybrid

Additional Details:

• Patient Facing Clinical Trials experience required
• Device Management Experience and Bench Trials experience not accepted

General Summary:

Under the supervision of the Supervisor, Manager, or Director of Clinical Research as appropriate, the Clinical Research Coordinator, the Senior CRC is responsible for supporting investigators during the conduct of multiple clinical research trials in accordance with the research center SOPs and all local, state, and federal regulations. Together with other team members, is responsible for coordinating enrollment, study visits and follow-up care of patients participating in clinical trials in various therapeutic areas. Acts as the liaison between the sponsor (monitor), regulatory agencies, patients, investigators, nurses and all other staff during the trial. Participates in internal and external quality audits.

Duties:

• Performs job functions timely and efficiently
• Acts as primary CRC for more complex protocols or patient populations
• Consistently exceeds minimum CRC workload index.
• Assists in training new research assistants and CRCs as needed.
• Demonstrates behaviors, which are consistent with the Code of Conduct and aligned with the organization's mission, vision and shared values
• Reports promptly any suspected or potential violations to laws, regulations, procedures, policies and practices, and cooperates in investigations.
• Conducts all transactions in compliance with all company policies, procedures, standards and practices.
• Demonstrates knowledge of all applicable compliance and legal requirements of the job based on the scope of practice of the position.
• Ensures that appearance and personal conduct are professional at all times:
• Excellent attendance record.
• Works at maintaining a good rapport and a cooperative working relationship with staff and physicians
• Represents the organization in a positive and professional manner in the community.
• Maintains organizational and patient confidentiality at all times.

Experience Required:

• Prefer to have a minimum of two years of experience in a Clinical Research setting where coordinator managed patients. Neurological conditions specialty a plus.
  
• Device trial experience will not be accepted. Solely data trials experience also not accepted.
• Minimum 5 years experience in a clinical research setting where candidate managed patients,
• **MUST HAVE EPIC EXPERIENCE** Must also have strong computer skills - Outlook, MS Teams, Word, Excel

Additional Information:

• Spanish/Korean speaking skills are a plus.
• Candidate commute is preferred to be 30 minutes or less due to traffic in the area.