Job Description
Are you ready to accelerate the development of life-changing therapies? Novus BioSciences AG is seeking a highly skilled and strategic Senior Clinical Research Associate (CRA) to join our dynamic team in Zurich. We are a global leader in biopharmaceutical innovation, dedicated to improving patient outcomes through rigorous clinical trial management.
In this pivotal role, you will oversee the initiation, execution, and close-out of clinical trials across multiple sites. You will act as a liaison between the sponsor, clinical investigators, and regulatory bodies, ensuring that every study meets the highest standards of quality, integrity, and compliance.
Why join Novus BioSciences?
- Competitive salary and comprehensive benefits package.
- Work with cutting-edge therapies in a collaborative environment.
- Professional development opportunities in a world-class pharmaceutical hub.
Responsibilities
- Manage the end-to-end clinical trial lifecycle, from site initiation to close-out, ensuring adherence to timelines and budgets.
- Conduct rigorous monitoring of clinical trials to ensure data integrity, patient safety, and protocol compliance in accordance with Good Clinical Practice (GCP).
- Act as the primary point of contact for Clinical Investigators and their study teams, fostering strong professional relationships.
- Prepare and submit clinical trial documentation, including Investigator Site Files (ISF) and annual safety reports.
- Monitor site performance and implement corrective action plans to mitigate risks and ensure study success.
- Collaborate with cross-functional teams including Data Management, Medical Writing, and Regulatory Affairs to ensure seamless trial execution.
- Facilitate communication between sponsors and regulatory authorities as required.
Qualifications
- Master’s degree in Pharmacy, Medicine, Nursing, Life Sciences, or a related field.
- 3-5 years of experience as a Clinical Research Associate in the pharmaceutical or biotechnology industry.
- Current RAC (Registered Clinical Research Associate) or CIP (Certified Clinical Research Professional) certification is highly preferred.
- Fluent in English and German (both written and verbal) is mandatory for this location.
- Strong working knowledge of ICH-GCP guidelines and regulatory standards (e.g., Swissmedic, FDA, EMA).
- Excellent organizational skills with the ability to manage multiple priorities and tight deadlines.
- Demonstrated ability to travel (up to 50%) to clinical trial sites within Switzerland and neighboring regions.