Job Summary
The position of Clinical Research Associate II/III is located in Boston, Massachusetts, and offers an onsite work arrangement. As a key member of a mid-sized, global Contract Research Organisation (CRO), you will play a significant role in advancing patient-centered clinical development through robust scientific practices.
Responsibilities
- Oversee and ensure compliance in clinical trials, ensuring that all regulatory requirements are met.
- Collaborate with potential investigators and institutions to develop study budgets effectively.
- Facilitate communication between study sponsors and site staff to ensure project milestones are achieved.
- Contribute to the overall operational excellence of clinical studies.
Qualifications
- A background in life sciences, nursing education, or a related healthcare field is preferred.
- Demonstrated experience in clinical research, with knowledge of applicable regulations and guidelines.
- Strong organizational and communication skills to effectively manage multiple tasks and liaise with diverse teams.
- Ability to work independently and collaborate in a team setting, adapting to the dynamic needs of clinical research.
