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.
