Clinical Trials Regulatory Specialist.

October 29, 2020

The Clinical Trials Regulatory Specialist is responsible and accountable for ensuring that inpatient and outpatient research protocols are coordinated through the regulatory process at study start-up and through the life of the study.

Job Description:

Full time
Knowledge in COFEPRIS Submission Process
Knowledge in Submitting to Local IRBs and Ethics Committees
Handling documents for the Regulatory Process
Preparing Documents for the Regulatory Process
Coordinating and assisting with contact database activities, including maintaining updated contact information for organization

Requirements:

Academic level of education; Bachelors Degree in areas related to Medical Science, Pharmacology, Biology or similar
2 Years Experience in Clinical Research Industry
Adequate command of written and spoken Spanish and English

Our vision is to become leaders in providing clinical research services in Latin America. Cohortias combines academic roots with our experience and a large pool of patients from an extensive network of sites. Join the Cohortias family in Mexico City!.

Apply here: https://www.linkedin.com/jobs/view/2249637449/

Cohortias – Your ally to conduct clinical research in Latin America.

Mexico Has Immense Clinical Research Capabilities And Benefits. Conducting Clinical Trials In Mexico Grants You Affordable Costs And A Robust Regulatory System.