Experienced Clinical Research Associate
Core
Conducting qualification, initiation, monitoring, and closeout visits for research sites to ensure compliance with protocols and regulatory requirements.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trials for pharmaceuticals and medical devices
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
Site monitoring, regulatory compliance (GCP/SOPs), medical record verification, adverse event assessment, protocol deviation management, investigator qualification verification
Preferred skills
Background in medical or science-related healthcare fields, experience in therapeutic areas
Technologies
None explicitly stated
Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits for research sites; Verify investigator qualifications, training, and resources; Verify medical record and research source documentation against case report forms; Verify investigator enrollment of eligible subjects; Review regulatory documents; Manage medical device and investigational product accountability; Assess adverse events and serious adverse events
Seniority
Entry-level to Mid-level (training provided for those without prior research experience)
