Sr. Clinical Research Associate (Germany)
- Role
- Research
- Experience
- Senior
Open to DE only. Set where you work from to check your eligibility.
No BS summary
Senior Clinical Research Associate for clinical site monitoring in Germany/Berlin. Must handle protocol/regulatory compliance under ICH/GCP and local regulation, sponsor/site liaison work, CRA assessment visits, audits/inspections, and mentoring CRA I/II.
Independently performs, coordinates and oversees all aspects of the clinical site monitoring services, assessing protocol and regulatory compliance as per Alimentiv’s and sponsor’s standard processes, ICH/GCP guidelines and local regulation. Serves as the primary liaison between the sponsor/Alimentiv and investigative sites by playing a critical role in the execution of clinical study plans. Provides guidance and mentoring CRA I and II, collaborating effectively with cross-functional stakeholders in a dynamic, results-driven and high-accountability environment. Perform CRA Assessment Visits and participate in audits/inspections, when required.
What you'll do
- Independently performs, coordinates and oversees all aspects of the clinical site monitoring services, assessing protocol and regulatory compliance as per Alimentiv’s and sponsor’s standard processes, ICH/GCP guidelines and local regulation.
- Serves as the primary liaison between the sponsor/Alimentiv and investigative sites by playing a critical role in the execution of clinical study plans.
- Provides guidance and mentoring CRA I and II, collaborating effectively with cross-functional stakeholders in a dynamic, results-driven and high-accountability environment.
- Perform CRA Assessment Visits and participate in audits/inspections, when required.
Healthcare company