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.
Thermo Fisher 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.
