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 2,500 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
Only CV's in English will be considered
We are looking for a CRA to join our team in Mexico. Here you will have the opportunity to develop yourself as a senior, 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.
Conduct onsite monitoring across clinical studies, oversee site communication and study progress, review clinical data, resolve queries, and support study startup and regulatory submissions.
Conduct onsite monitoring across Phase II and III clinical studies, manage site communications and study documentation, and coordinate with project teams, vendors, and support services.
Conduct onsite monitoring across Phase II and/or III clinical studies, manage site communications and study progress, and support study startup, data review, feasibility, and regulatory submissions.
Conduct clinical study monitoring across therapeutic areas, manage site communications and study progress, review clinical data, resolve queries, and support feasibility research and regulatory submissions.
Monitor clinical studies at investigative sites or remotely, ensuring trials are conducted, documented, and reported in compliance with protocols, SOPs, ICH-GCP, and applicable regulations.
