Job Summary
The individual in this role will oversee and coordinate research trials, ensuring effective participant recruitment and adherence to study protocols. This includes the management of biological samples and the maintenance of meticulous study records while ensuring adherence to regulatory guidelines.
Responsibilities
- Coordinate and oversee all aspects of research trials.
- Facilitate participant recruitment and manage study procedures.
- Handle biological specimens and uphold the integrity of study records.
- Ensure compliance with regulatory standards and study protocols.
Qualifications
- A Bachelor’s degree or an equivalent combination of education and experience is necessary.
- 1-3 years of relevant experience in a related field.
- A minimum of 2-3 years specifically in clinical research is required.
Northwell 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.
