Fortrea

Analytics Corrective Action GCP Performance Management Process Improvement +2 skills

Manager, Centralized Monitoring

RemoteAPAC, LATAM

Job Overview: Reviews trip reports, proactively identifies risks and communicate any trends, outstanding issues, safety concerns to the study team. Responsible for the execution of key Central monitoring activities…

Associate Manager, Clinical Research

LATAM

Job Overview: The aCRM is accountable for execution and oversight of local operational clinical trial activities and has ownership, oversight and impact on local regulatory and financial compliance, at a country…

GCP

Project Manager Drug Safety

LATAMFellowship

Data Quality GCP Regulatory Compliance

Job Overview: Manage ‘Client’ or ‘Project’ specific PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post…

Clinical Trial Coordinator (Finance / Supplies)

LATAMContract

ERP Financial Reporting GCP Stakeholder Management

Job Overview The Clinical Trial Coordinator (CTC) serves as a key liaison between investigative sites, sponsors, vendors, and internal study teams, supporting financial and operational activities throughout the…

last month

Clinical Research Associate II

LATAM

Corrective Action GCP Technical Writing

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including…

GCP Microsoft Project Risk Assessment Vendor Management

last month

Project Coordinator I

Open 36d LATAMContract

Job Overview: The mission of the Project Management Academy (PM Academy) is to identify and develop potential clinical project management leaders of the future. Within a face-to-face, continuous learning environment,…

2 months ago

Medical Contact Center Assistant I

Open 58d LATAM

Summary of Responsibilities: To respond to medical information queries/product quality complaints/general queries that may be received over the telephone call, email, fax etc. Receive information, record, and report…

GCP

Open 99d LATAMFellowshipSenior

5 months ago

Senior Drug Safety Associate

Data Quality GCP Process Improvement Regulatory Compliance

Job Overview: Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post…