Job Summary
The Clinical Research Associate II is responsible for fostering collaborative partnerships with investigational sites in the realm of clinical research. This role requires a keen understanding of clinical operations and the ability to navigate complex trial protocols effectively.
Responsibilities
- Establish and maintain strong working relationships with various investigational sites.
- Oversee the integrity and accurate execution of clinical research protocols.
- Ensure compliance with regulatory guidelines and company policies.
- Provide guidance and support to site personnel throughout the trial process.
- Monitor patient enrollment and data quality to meet study objectives.
Qualifications
- A Bachelor’s degree in a relevant scientific discipline or a Registered Nursing certification.
- Experience in clinical research, preferably in a monitoring role.
- Strong understanding of Good Clinical Practice (GCP) and relevant regulatory requirements.
- Excellent communication and interpersonal skills to collaborate effectively with investigators and site staff.
- Proficiency in clinical trial management software and data entry systems.
