Thermo Fisher Scientific

Thermo Fisher Scientific Hiring for Trial Activation Approval Specialist I

by

Thermo Fisher Scientific Hiring for Trial Activation Approval Specialist I

Trial Activation Approval Specialist I

Location Remote, India Job Id R-01286846 Job Type Full time Category Clinical Research Remote Fully Remote

Our team of colleagues in clinical research services are at the forefront of getting cures to market. We bring a high caliber of scientific and clinical expertise to the development of drugs that address the world’s most challenging health concerns. Our Clinical Research team, who powers our PPD® clinical research portfolio, are part of our leading global contract research organization (CRO). 

Work Schedule

Standard (Mon-Fri) 

Environmental Conditions

Office 

Job Description

Are you ready to embark on a fulfilling career journey with Thermo Fisher Scientific Inc.? We are looking for a motivated and ambitious individual to join our PPD team as a Country Approval Specialist?. This outstanding opportunity allows you to contribute to world-class clinical trials, making a significant impact on global clinical research.

Responsibilities

  • Prepares and performs the submissions to competent authorities including the ethics committees.
  • Collect essential documents for the trial and sites assigned.
  • Reviews, prepares the IP greenlight packages and works with the study team for the site activation readiness.
  • Drive timely clinical trial site activations. Ensure all trial activations are flawless and comply strictly with regulatory standards.
  • Collaborate with cross-functional teams. Work closely with research sites, regulatory, and clinical operations teams to successfully implement trial activation plans.
  • Maintain comprehensive documentation. Keep meticulous records of all trial activation processes and approvals.
  • Identify and address potential issues: Determine any barriers to trial activation and collaborate with teams to resolve them promptly

 

Requirements

  • Educational background: Bachelor’s degree or equivalent experience in Life Sciences, Pharmacy, or a related field.
  • Experience: Proven experience in clinical trial management, study startup activities or a related research role is preferred.
  • Skills: Outstanding attention to detail, strong organizational skills, and the ability to work collaboratively in a fast-paced, dynamic environment, understanding of clinical trial requirements, regulation and GCP guidelines. .
  • Communication: Excellent verbal and written communication skills to effectively interact with diverse teams, collaborators, and customers.
  • Technical proficiency: Familiarity with clinical trial management systems and regulatory requirements.

 

Join us on our mission to enable our customers to make the world healthier, cleaner, and safer. Your expertise and dedication will contribute to our continued success and innovation in the scientific community.

APPLY HERE

To Join In Whatsapp group Click below Link

https://chat.whatsapp.com/ERzsuXoDDnOLBZ3spkddn5

 

To Join Telegram Channel Click Below Link

https://t.me/careerpathwayjobs

To know the Latest Job updates  click below Link

Career Pathway – Guide to your success

Leave a Comment