Clinical Research Associate (Pharm D Candidates)
Core
Conduct qualification, initiation, monitoring, and closeout visits at clinical research sites to ensure compliance with protocols and regulatory requirements.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for pharmaceutical and medical device development
Domain
Clinical research / Biopharmaceuticals
Deliverable
client delivery
Required skills
Protocol compliance, site monitoring, regulatory document review, adverse event verification, subject eligibility verification, data documentation verification
Preferred skills
Pharm D degree, Microsoft Office proficiency
Technologies
Clinical Trial Management System
Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits at research sites; Verify investigator qualifications and resources; Review medical records and source documentation against case report forms; Monitor adverse events and concomitant medications; Assess patient recruitment and retention success
Seniority
Entry-level to Junior, training provided