Job Description
Are you a dedicated professional passionate about accelerating life-changing therapies? Novabio Therapeutics is seeking a highly skilled Senior Clinical Research Associate (CRA) to join our dynamic Clinical Operations team in the heart of Basel. We are at the forefront of biotechnology innovation, dedicated to developing breakthrough treatments for complex diseases.
In this pivotal role, you will oversee clinical trial sites, ensuring compliance with Good Clinical Practice (GCP) and regulatory standards while maintaining the highest standards of patient safety and data integrity. If you thrive in a fast-paced, collaborative environment and want to make a tangible impact on global healthcare, we want to hear from you.
Why Join Us?
- Work with a world-class team of scientists and medical experts.
- Competitive compensation package in CHF.
- Opportunities for professional growth and leadership development.
- State-of-the-art facilities in the Basel BioValley.
Responsibilities
- Monitor clinical trial sites to ensure adherence to protocol, Good Clinical Practice (GCP), and regulatory requirements.
- Conduct regular site visits, including monitoring visits, initiation visits, and close-out visits.
- Review and validate clinical data for accuracy, completeness, and timeliness.
- Manage communication between the sponsor, investigators, and study staff effectively.
- Identify and resolve clinical, operational, and regulatory issues in a timely manner.
- Prepare and submit clinical study reports and regulatory documents.
Qualifications
- Master’s degree in Life Sciences, Pharmacy, Medicine, or related field; Bachelor’s degree with significant experience may be considered.
- Minimum of 3-5 years of experience in Clinical Research, ideally within the pharmaceutical or biotechnology industry.
- Valid GCP certification (e.g., AAHRPP/ECOG) is mandatory.
- Fluency in English (written and verbal); German is a strong asset.
- Willingness to travel extensively (up to 75%) to trial sites across Europe.
- Strong analytical skills and attention to detail.
- Excellent interpersonal and stakeholder management abilities.