Clinical Research Associate

We are looking for an experienced Clinical Research Associate to join the Roche team in our efforts to develop and improve our treatments. As a Clinical Research Associate, you will be responsible for monitoring clinical studies to ensure compliance with Good Clinical Practices (GCPs). The ideal candidate will have a Bachelor's Degree in a relevant field and a minimum of two years' experience in clinical research. A strong understanding of medical terminology and the ability to effectively communicate both orally and in writing are also essential. If you are detail-oriented, have a passion for clinical research, and want to help Roche develop treatments that improve the lives of patients around the world, this may be the perfect opportunity for you.

Responsibilities:

1. Monitor clinical studies to ensure GCP compliance.
2. Maintain records and provide progress reports on study status.
3. Communicate with investigators and other clinical research staff.
4. Ensure accurate and timely data collection, entry, and management.
5. Prepare and submit safety reports to the regulatory authorities.
6. Review and evaluate clinical protocols and amend as necessary.
7. Assist in the preparation of submissions for regulatory approval.
8. Participate in the development of study budgets and timelines.
9. Support the development of new protocols and modifications to existing protocols.
10. Participate in clinical site selection and initiation visits.
11. Monitor study progress and provide ongoing support to investigators.
12. Develop and maintain relationships with clinical investigators.
13. Develop and maintain effective working relationships with sponsors.
14. Provide input to the development of clinical research materials.
15. Manage the collection, review, and submission of study documents.
16. Identify and resolve any issues that may arise during the course of the study.

According to JobzMall, the average salary range for a Clinical Research Associate in South San Francisco, CA, USA is between $97,000 and $125,000 per year. The average hourly wage for this position is between $45 and $60 per hour. Job duties typically include conducting clinical trials, reviewing data, developing protocols, and providing feedback to clients and sponsors. Additional skills that can increase salary range include project management, regulatory affairs, and experience in clinical trial management.

Roche Holding AG operates as a research healthcare company. It operates through the diagnostics and pharmaceuticals segments. The pharmaceutical segment refers to development of medicines in the field of oncology, immunology, ophthalmology, infectious diseases and neuroscience. The diagnostic segment refers to diagnosis of diseases through an in vitro diagnostics process.