SUMMARY:

Clinical Research Coordinator (CRC) is responsible for conducting trials as per the GCP guidelines under the supervision of the Principal Investigator (PI). In addition to providing and coordinating clinical care, a CRC has a central role in assuring subject safety, ongoing maintenance of informed consent, integrity of protocol implementation, accuracy of data collection, data recording and follow up.
Care received by research subjects is driven by study requirements and the collection of research data as well as clinical indications. The CRC’s goal is to protect subjects participating in clinical trials, promote good clinical practices and professional management of clinical studies.

KNOWLEDGE, SKILLS AND ABILITIES:

• Exceptional attention to detail with strong interpersonal skills.
• Excellent verbal & written communication and organizational skills.
• Ability to manage multiple tasks and prioritization
• Must be proficient in Excel, Microsoft Office, and other computer programs.

EDUCATION:

• Certified Medical Assistant, associate’s degree in health care field and/or equivalent experience in the healthcare industry.
• Certification as Clinical Research Coordinator through ACRP (CCRC) or SoCRA (CCRP). Consideration for applicants who are qualified to be certified.
• Clinical Research Coordinator with 2 or more years’ experience preferred. Clinical skills, including the ability to perform phlebotomy, vital signs, EKG’s, injections etc.
  Job Type: Full-time
  Expected hours: 40 per week

Benefits:

• 401(k)
• Dental insurance
• Employee assistance program
• Flexible spending account
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Referral program
• Vision insurance

Work Location: In perso

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