Independent Contractor / Freelance - Clinical Research Associate (CRA)
Core
Conducting qualification, initiation, monitoring, and closeout visits for clinical research sites to ensure compliance with protocols and regulations.
Role type
Independent Contractor Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for pharmaceutical and medical device development
Domain
Clinical Research / Life Sciences
Deliverable
physical/clinical work
Required skills
Clinical monitoring, protocol adherence, source documentation verification, adverse event reporting, patient recruitment assessment, regulatory document review, investigational product accountability (via careerplan.io/jobs/13044-independent-contractor-freelance-clinical-research-associate-cra-at-medpace)
Preferred skills
Experience in oncology, cardiology, metabolic, endocrinology, CNS, anti-viral, or anti-infective therapeutic areas
Technologies
Case Report Forms (CRF), Investigator Site Files (ISF), Trial Master Files (TMF)
Responsibilities
Conduct site qualification, initiation, monitoring, and closeout visits; Verify investigator qualifications and resources; Review medical records and source data against CRFs; Monitor adverse events and concomitant medications; Assess patient recruitment and retention; Complete monitoring reports and follow-up letters.
Seniority
Mid-Senior, hands-on IC