Site Management Associate (Clinical Trials)
This role offers the chance to gain extensive clinical operations experience by serving as a key contact for investigative sites and supporting clinical study delivery.
We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,800 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information.
Only CVs in English will be accepted.
You will be responsible for:
Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.
This role offers the chance to gain extensive clinical operations experience by serving as a key contact for investigative sites and supporting clinical study delivery.
Coordinate clinical research site operations by supporting site teams and monitors, managing study documentation and supplies, tracking issues, and ensuring regulatory submissions and safety information flow.
Provide remote scheduling and administrative support for Veterans by coordinating appointments and referrals, maintaining accurate healthcare records, and communicating with patients, providers, and internal teams.
Operate a First Response Unit ambulance as a volunteer, responding to time-critical emergencies and providing immediate patient care until frontline ambulance crews arrive.
Support clinical research projects by streamlining communication, maintaining systems, and managing documents to ensure project success.