Senior Clinical Research Associate
Core
Conduct onsite monitoring visits, manage study timelines, and ensure data compliance and subject safety across Phase I-III clinical trials.
Role type
Senior Clinical Research Associate (Oncology focus)
Builds
Clinical trial data integrity and regulatory compliance for medical science projects
Domain
Clinical Research / Oncology / Radiopharmaceuticals
Deliverable
client delivery
Required skills
Independent onsite monitoring, Phase I-III trial experience, complex Oncology trial monitoring, radiopharmaceuticals experience, breast cancer trial experience, GI studies experience (IBD, Chron's, UC), MS Office proficiency, travel management, regulatory document preparation
Preferred skills
Radiopharmaceuticals experience, breast cancer experience, GI studies experience
Technologies
MS Office
Responsibilities
Conduct and report all types of onsite monitoring visits, Perform CRF review and source document verification, Supervise study activities and schedules on the country level, Support regulatory team in preparing documents for study submissions, Participate in feasibility research (via careerplan.io/jobs/744000130795524-senior-clinical-research-associate-at-psi-cro)
Seniority
Senior, hands-on IC