Clinical Research Associate (CRA) 60-80% — Universität Bern
- Location
- Bern
- Contract
- full-time
- Posted
- 2 days ago
Role overview
UniBE is networked.
- UniBE is networked.
- Support for the planning, organisation and implementation of the clinical trial
- Submission of documents to the Ethics Committee (BASEC) and Swissmedic
- With us you are part of an international community and benefit from interdisciplinary cooperation.
Main responsibilities
- Support for the planning, organisation and implementation of the clinical trial
- Submission of documents to the Ethics Committee (BASEC) and Swissmedic
- Preparation and maintenance of study-relevant documents (e.g.
- Investigator Site File, Trial Master File, SOPs, QMS)
- Monitoring regulatory compliance, ICH-GCP guidelines and study protocol
- Data collection and maintenance in electronic study databases (eCRF) and data quality assurance
- Close exchange with study centers, including regular center visits Support and training of study teams Initiation of study centres
- Conduct of monitoring visits and documentation and tracking of deviations Requirements
- Completed training in health care or natural sciences
- Experience in clinical research (including Good Clinical Practice Certificate) Interest in the topic
What the company offers
- With us you are part of an international community and benefit from interdisciplinary cooperation.
Additional details
- Close exchange with study centers, including regular center visits Support and training of study teams Initiation of study centres
- Conduct of monitoring visits and documentation and tracking of deviations
- Experience in clinical research (including Good Clinical Practice Certificate) Interest in the topic
- Initiative, reliability and organisational capacity High quality awareness
- Experienced handling of MS-Office and databases (e.g.
- Good teamwork skills and good communication skills
Notes and original content
- Close exchange with study centers, including regular center visits
- Support and training of study teams
- Initiation of study centres
- Requirements
- Experience in clinical research (including Good Clinical Practice Certificate)
- Interest in the topic
- Initiative, reliability and organisational capacity
- High quality awareness
- REDCap, SecuTrial)
Questions about this listing
What salary does Universität Bern offer for this role?
Universität Bern lists CHF 54'800 - 83'200 gross per year for this position in Bern. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Universität Bern offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Universität Bern during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Bern?
EU/EFTA residents living in the border zone of the country adjoining Canton Bern can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Bern's cantonal migration office or with HR during the application.
How do I apply for this position at Universität Bern?
Use the "Apply now" button on this page — it links directly to Universität Bern's original listing at jobs.unibe.ch, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
