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 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
We are looking for an experienced CRA ready to train and coordinate junior CRAs on site. Here you will have the opportunity to develop yourself as a trainer, mentor and leader. We are committed to develop our employees in their careers by providing tailored courses and mentoring.
Responsibilities will include:
If you like to train and support others on their clinical research steps, and are also looking forward to future Lead Monitor roles, this position may just be the right one for you.
Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with a rapid growing company that puts its people first.
Oversee clinical trial monitoring from pre-study through close-out, assess investigator site readiness, train site staff, support regulatory submissions, and mentor junior clinical research staff.
Oversee clinical trial monitoring from site qualification through close-out, train site staff, support regulatory submissions, and mentor junior colleagues across complex Phase 2/3 studies.
Independently oversee clinical trial monitoring from site initiation through close-out, maintaining GCP and regulatory compliance, strong investigator relationships, data quality, and trial integrity.
Monitor clinical trials across therapeutic areas, serving as the primary link between study teams, sponsors, and sites while ensuring site-level quality, compliance, data integrity, and study timelines.
Conduct clinical trial monitoring and site management across onsite and remote visits, taking ownership of study delivery, site performance, and quality while supporting strong site relationships.
