Job Summary
The Clinical Research Associate (CRA) plays a vital role in ensuring the quality, compliance, and effective execution of clinical trials. This position involves participating in site visits, co-monitoring, interacting with investigators at meetings, and supporting selected international initiatives, particularly within the fields of life sciences, nursing, pharmacy, or a closely related discipline.
Responsibilities
- Ensure compliance and quality standards throughout the clinical trial process.
- Conduct site visits and co-monitoring activities to assess trial conduct.
- Facilitate communication during investigator meetings and collaborate with site personnel.
- Contribute to international project activities as required.
Qualifications
- A minimum of 4 years of experience in clinical research.
- Educational background in life sciences, nursing, pharmacy, or a closely related field.
- Strong understanding of clinical trial protocols and compliance norms.
- Excellent communication and organizational skills.
Monte Rosa Therapeutics provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
