Job Summary
The position of an On-site Clinical Research Associate is available in Newark, California. This role is integral to the collaborative efforts between Protagonist and Johnson & Johnson scientists, focusing on the advancement of clinical research initiatives with Protagonist taking the lead in development activities.
Responsibilities
- Engage in clinical research protocols and their implementations.
- Collaborate with research teams to ensure compliance with regulations.
- Monitor clinical trials to maintain high-quality standards and data integrity.
- Assist in the preparation and submission of regulatory documents.
- Contribute to the analysis and reporting of clinical study results.
Qualifications
- A degree in life sciences or a related field.
- Previous experience in clinical research or monitoring role.
- Strong understanding of clinical trial regulations and guidelines.
- Excellent communication and interpersonal skills.
- Ability to work collaboratively within a team environment.
