Clinical Research Associate - Oklahoma, US

Industry: Medtech, Digital Health

Job Functions: Site Monitoring for clinical trials with medical device

Location: Oklahoma, USA

Workplace: remote/availability to travel

Meditrial is seeking a certified Clinical Research Associate (CRA) with extensive experience in medical device clinical trials to join our dynamic team. The CRA will be responsible for monitoring Phase I-IV clinical trials, ensuring compliance with Good Clinical Practices (GCP) and study protocols. This role involves conducting site evaluations, initiation, interim, and close-out visits, as well as collaborating closely with Clinical Project Managers and CTAs.

The ideal candidate will have a proven track record in medical device trials, particularly in cardiology, and must be available to travel for monitoring activities as needed.

Responsibilities

• Conduct on-site and remote monitoring visits from SIV (Site Initiation Visit) to COV (Close-Out Visit), ensuring study sites adhere to protocols and regulatory requirements.
• Train investigators and site personnel on study protocols and best practices.
• Review Case Report Forms (CRFs) and verify entries against source documentation.
• Document site visits, findings, and follow-ups in detailed reports.
• Facilitate communication among investigative sites, sponsors, and internal teams.
• Identify and assess potential investigators in collaboration with sponsors.
• Ensure compliance with FDA, ICH-GCP, and local regulatory guidelines.
• Assist in study submissions and preparation of regulatory documents.
• Support project teams with study communications and trial management activities.
  
  
  

• 6+ years of experience in clinical trial monitoring for CROs and Sponsors, with a strong focus on medical device trials.
• Expertise in cardiology trials and experience across other therapeutic areas.
• Higher or specialized degree in natural sciences (e.g., Biology, Medicine, Pharmacy, or related fields).
• CRA Certification with a track record of successful monitoring visits.
• Proficiency in electronic CRF (eCRF), CTMS systems, and other digital tools.
• Background in CROs, pharmaceuticals, biotechnology, and medical devices.
• Fluency in English (a second language is a plus).
• Willingness to travel as required for site visits and monitoring activities.