October 12, 2024

Thermo Fisher Scientific

Lagunilla

OTHER

Principal CRA

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description

What Makes This Opportunity Unique

Thermo Fisher Scientific offers a role with global impact. As a Principal CRA, you will play a vital part in our research initiatives, ensuring precise and regulatory-compliant clinical trials. Take the lead in critical studies to drive scientific progress and improve patient outcomes.

Job Responsibilities

Monitor and coordinate all site activities to ensure flawless execution.
Manage study data, including the review and tracking of study documents, drafting, compiling, and verifying clinical data for status reports.
Serve as the primary contact for study sites, promoting collaboration and inclusion.
Track distribution and accountability of study drugs and clinical supplies.
Ensure the trial is conducted, detailed, and reported according to the protocol, FDA GCPs, Global SOP/WPDs, ICH Guidelines, and regulatory requirements.
Ensure study timelines and deliverables are met strictly within contract time.

Job Requirements

RPh or equivalent experience, Bachelor’s degree or equivalent experience in life sciences or related field or certification in a related allied health profession from an appropriately accredited institution (e.g., RN, MT, PA, RPh, RT).
Proven experience in clinical research and trial management.
Outstanding organizational and communication skills.
Ability to collaborate with diverse teams and compete in a fast-paced environment.
Strong attention to detail and dedication to quality.