Sr CRA Analyst I

at  Thermo Fisher Scientific

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.

• 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.