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:

Being the main point of contact between site personnel and CRA involved in the project helping on query resolution and EDC completion
Serves as the primary sites’ contact point for vendors, study supplies, and access management
Ensure that pre-study testing (scans, MRI/CT qualification questionnaires, test ECGs, etc.) of local site facilities is completed
Assists the Monitors in their prompt completion of all subject event and site event information in CTMS. Track the resolution status of site issues and action items in CTMS
Act as the one who will ensure the order, receipt, inventory storage, distribution, return/recall and reconciliation of clinical supplies
Ensures regulatory and ethics committee submissions and notifications, meaning you will need to be up to date on local regulations and dispositions
Coordinate preparation for and follow-up on site, TMF and systems´ audits and inspections
Manage the TMF on a site and a country level regularly and file documents. Prepare, distribute, and update Investigator Site Files (ISF) and ISF checklists
Arrange and track initial and on-going project training for site teams in all vendor-related systems
Document Management and translations status review of the study
Ensures proper safety information flow with investigative sites

College/University Degree in Life Sciences;
Administrative work experience, preferably in an international settings;
Prior experience working as CTA for CROs;
Prior experience working in Clinical Research;
Local regulations knowledge;
Full working proficiency in English and Spanish;
Proficiency in MS Office applications;
Ability to plan and work in a dynamic team environment;
Communication and collaboration skills.

Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.

Newsletter