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Senior Clinical Research Professional
2 weeks ago
As a key member of our clinical research team, you will be responsible for ensuring the successful execution of clinical trials. This involves setting up and monitoring studies, completing reports, and maintaining accurate documentation.
Key Responsibilities:- Set up and monitor studies to ensure compliance with regulatory requirements
- Prepare and review study documentation, including protocols and consent forms
- Maintain accurate records and complete reports in a timely manner
- Identify and mitigate risks associated with trial conduct
- 12 months+ of experience in clinical research, preferably as a CRA
- Degree in medicine, science, or equivalent
- Excellent written and verbal communication skills in English and German
- Able to work independently and as part of a team
- Highly organized and able to prioritize tasks effectively
- Competitive salary and benefits package
- Opportunities for professional growth and development
- Flexible working arrangements to support work-life balance
- Global Employee Assistance Programme
We are committed to creating an inclusive and accessible environment for all candidates. If you have any questions or concerns, please do not hesitate to contact us.
