Senior Clinical Research Associate
P
Precision for MedicineClinical Trial Services
Poland, Hungary, United Kingdom, France and GermanyFull-TimeSenior
Salary not disclosed
Apply NowOpens the employer's application page
Job Details
- Languages
- Fluency in English and the local language is required
- Experience
- Minimum 5 years of CRA/SCRA experience
Requirements
- 4-year college degree or equivalent experience.
- Holder of CRA certificate.
- Minimum 5 years of CRA/SCRA experience within a CRO, pharmaceutical, biotechnology, or medical device environment.
- Experience monitoring clinical trials across a variety of therapeutic areas.
- Availability for domestic travel including overnight stays, up to approximately 50-60% travel commitment.
- Fluency in English and the local language is required.
- Understanding of financial management for Senior CRAs (preferred).
- Study start-up activities experience (preferred).
Responsibilities
- Monitor and own the progress of clinical studies at investigative sites.
- Ensure clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations.
- Coordinate all necessary activities required to set up and monitor a study, including identifying investigators and preparing regulatory submissions.
- Support clinical study teams with trials larger in scope.
- Train and mentor junior staff members.
- Interact directly with clients and initiate payments.
- Participate in proposal activities, including development and client presentations.
View Full Description & ApplyYou'll be redirected to the employer's site
