Clinical Research Associate (CRA) - Dallas
Core
Conduct qualification, initiation, monitoring, and closeout visits at clinical research sites to ensure compliance with protocols and regulations for pharmaceutical and medical device trials.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for biotechnology, pharmaceutical, and medical device companies
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Medical record verification, regulatory document review, adverse event reporting, site compliance monitoring, patient recruitment assessment, inventory management
Preferred skills
Nursing, Dietetics, Pharmaceutical Sales, Physical Therapy, Biomedical Engineering, Public Health, PhD, Pharm.D
Technologies
Clinical Trial Management System, Microsoft Office
Responsibilities
Conduct on-site and virtual monitoring activities to identify site deviations and mitigate risks; Verify investigator qualifications and resources; Review medical records and source documentation against case report forms; Assess patient recruitment and retention success; Complete monitoring reports and follow-up letters regarding significant findings and deviations.
Seniority
Entry-level to Mid-level, training provided