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.
Optimapharm d.o.o. 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.
