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Trial Activation Approval Specialist I

AT Thermo Fisher Scientific
Thermo Fisher Scientific

Trial Activation Approval Specialist I

Remote

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

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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.

Job ID: ThermoFisher-R-01286846
Employment Type: Full Time

Perks and Benefits

  • Health and Wellness

    • Health Insurance
    • Dental Insurance
    • Vision Insurance
    • Life Insurance
    • Short-Term Disability
    • Long-Term Disability
    • FSA
    • HSA
    • HSA With Employer Contribution
    • Mental Health Benefits
    • Fitness Subsidies
  • Parental Benefits

    • Adoption Leave
    • Birth Parent or Maternity Leave
    • Non-Birth Parent or Paternity Leave
    • Fertility Benefits
    • Adoption Assistance Program
    • Family Support Resources
  • Work Flexibility

    • Flexible Work Hours
    • Hybrid Work Opportunities
    • Remote Work Opportunities
  • Office Life and Perks

    • Commuter Benefits Program
    • On-Site Cafeteria
  • Vacation and Time Off

    • Paid Vacation
    • Paid Holidays
    • Volunteer Time Off
  • Financial and Retirement

    • 401(K) With Company Matching
    • Stock Purchase Program
    • Financial Counseling
    • Performance Bonus
  • Professional Development

    • Tuition Reimbursement
    • Access to Online Courses
    • Internship Program
    • Mentor Program
  • Diversity and Inclusion

    • Employee Resource Groups (ERG)
    • Diversity, Equity, and Inclusion Program