Clinical Research Associate at PSI CRO

Ciudad de México, , Mexico -

Full Time

Start Date

Immediate

Expiry Date

24 Jul, 26

Salary

0.0

Posted On

25 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical research, Site monitoring, Source document verification, CRF review, Query resolution, Regulatory affairs, Site management, Investigator training, Feasibility research, Audit preparation, MS Office, Communication, Collaboration, Problem-solving, Project management

Industry

Pharmaceutical Manufacturing

Description

Company Description 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. Job Description 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: Preparation, conduct, and reporting of selection, initiation, routine and closeout monitoring visits Delivering training of investigators, site staff and project teams Work with complex studies Perform CRF review, source document verification and query resolution Be responsible for site communication and management Be involved in site identification process Contact for clinical investigators, vendors and support services in regard to study progress Participate in feasibility research Preparation and delivering of presentations at Investigator’s Meetings Preparation for and attendance at company’s audits; resolution of audit findings Support to Regulatory Affairs in procurement of site regulatory documents Maintenance of study-specific automated tracking systems Qualifications College/University Degree in Life Sciences; At least 2 years experience in patient care and/or health care or clinical environment Full working proficiency in English Experience in Clinical Research is a plus Availability to travel Proficiency in MS Office applications Ability to plan and work in a dynamic team environment Communication, collaboration, and problem-solving skills Additional Information 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.

Responsibilities

The Clinical Research Associate is responsible for the preparation, conduct, and reporting of clinical monitoring visits and site management. They will also facilitate investigator training, manage study-specific tracking systems, and support regulatory document procurement.