Senior Clinical Research Associate
P
Precision for MedicineClinical Trial Services
Poland, Hungary, United Kingdom, France and GermanyFull-TimeSenior
Salary not disclosed
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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.
- Fluency in English and the local language.
- Availability for domestic travel including overnight stays (up to approximately 50-60% commitment).
- Understanding of financial management for senior level.
- Study start up activities experience (preferred).
- Graduate or postgraduate degree in a scientific or healthcare discipline (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 applicable regulations.
- Coordinate activities for study setup including investigator identification and regulatory submissions.
- Conduct pre-study and initiation visits.
- Manage clinical trials of appropriate size and support larger trials.
- Train and mentor junior staff members.
- Interact directly with clients, initiate payments, and participate in proposal activities.
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