Clinical Research Associate
Remote · from Germany
Core
Monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocol, SOPs, and regulations.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trials for oncology and rare disease
Domain
Biopharmaceuticals / Clinical Research
Deliverable
client delivery
Required skills
Site management, regulatory submissions, risk identification, conflict resolution, study monitoring, protocol adherence
Preferred skills
Study start-up, CAR-T, FIH phase III, medical device
Technologies
ICH-GCP, SOPs
Responsibilities
Conduct pre-study and initiation visits, coordinate study setup activities, monitor study progress at sites, ensure data recording and reporting per protocol, identify and mitigate study risks
Seniority
Entry to Mid-level
