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Senior Clinical Research Associate

Posted 2 years ago in Research & Dev



A dynamic and growing CRO is looking for a regional CRA. Responsibilities include but are not limited to: performing monitoring visits including site qualification, initiation, monitoring and close-out visits; maintaining regular contact with study site to ensure protocol/GCP compliance; participating in Investigator meetings and other study training meetings as required; preparing for and participating in Sponsor and FDA audits.

Required qualifications:
  • Proven success in monitoring clinical trials in the pharmaceutical industry and a 4 year degree in a sciences or health related field is necessary (an R.N. with solid monitoring experience will also qualify);
  • Minimum 6 years field monitoring experience;
  • Oncology monitoring experience a plus
  • Strong understanding of Medical Terminology, Physiology, and Pathophysiology;
  • Working knowledge of Good Clinical Practices;
  • Strong organizational skills;
  • The ability to multi-task and to work independently and effectively in a fast-paced environment;
  • Strong written and verbal communication and diplomacy skills;
  • Must have ability to submit travel receipts for bi-monthly reimbursement;
  • Professional demeanor and appearance; ability to travel up to 75%.

Education, employment history, professional references and certifications/training will be verified prior to offer of employment.

About MedSource:

MedSource is recognized as a niche clinical research organization (CRO) focusing on complex clinical trials, with a particular expertise in conducting oncology clinical trials.

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