Job Summary
The Clinical Research Associate II/III plays a vital role in the execution and management of clinical trials. This position involves working closely with clinical sites to ensure that studies are conducted in compliance with regulations, protocols, and company standards. The successful candidate will contribute to the overall success of clinical research initiatives by overseeing monitoring activities and ensuring data integrity throughout the study lifecycle.
Responsibilities
- Conduct site monitoring visits and ensure adherence to study protocols.
- Review and verify clinical trial data for accuracy and compliance.
- Assist in the preparation and submission of regulatory documents.
- Provide support in training site personnel on study protocols and procedures.
- Collaborate with cross-functional teams to facilitate project timelines and objectives.
Qualifications
- Bachelor’s degree in life sciences or a related field.
- Previous experience in clinical research, with specific knowledge of GCP and ICH guidelines.
- Strong organizational and problem-solving skills.
- Excellent communication abilities, both written and verbal.
- Proficiency in using clinical trial management systems and electronic data capture tools.
