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Thermo Fisher Scientific

Compare

3.9

based on 802 Reviews

155 Thermo Fisher Scientific Jobs

Trial Activation Approval Specialist I

PPD

3.9

based on 802 Reviews

3-7 years

Kolkata, Mumbai, New Delhi + 4 more

1 vacancy

Trial Activation Approval Specialist I

Thermo Fisher Scientific

posted 1d ago

Job Role Insights

Flexible timing

Key skills for the job

Pharmacy Research Clinical Research Life Sciences Packaging GCP

+ 2 more

Job Description

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.

Employment Type: Full Time, Permanent

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