Job Summary
The role of Senior Clinical Research Associate is focused on advancing healthcare intelligence within a clinical research organization devoted to its mission. This position involves close collaboration with investigators and site personnel to streamline the research process, contributing significantly to various clinical studies.
Responsibilities
- Collaborate with investigators and site staff to enhance the efficiency of clinical studies.
- Facilitate effective communication between all parties involved in the research process.
- Support clinical trial operations using expertise from prior experience, particularly in a study coordinator or nursing capacity.
Qualifications
- A minimum of 1 year of experience in clinical research roles, preferably as a study coordinator or nurse.
- Strong understanding of clinical trial protocols and procedures.
- Excellent communication skills for effective collaboration with site and study personnel.
ICON plc 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.
