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the right place for you

We are vital links. Between an idea for a new medicine and the people who need it. 

We are Cohortias — a niche CRO motivated by bringing Clinical Research to regions that needs it the most. 

Hands-on Positions

Clinical Operations

Clinical Research Associate II (CRA II)
Based in Mexico City

The CRA II based in Mexico City, will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol.

This role will be based in Mexico City

Key responsibilities include:

• Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out.

• Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan.

• Developing effective relationships with investigator site staff to ensure that key clinical metrics are met.

• Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues.

• Ensuring the integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines.

Requirements:

• Prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment.

• Working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential.

Clinical Research Associate II (CRA II)
Based in Bogota, Colombia

The CRA II based in Bogota (working from home), will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol.

This role will be based in Bogota, Colombia

Key responsibilities include:

• Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out.

• Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan.

• Developing effective relationships with investigator site staff to ensure that key clinical metrics are met.

• Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues.

• Ensuring the integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines.

Requirements:

• Prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment.

• Working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential.

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