Trial Activation Approval Specialist I
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
Want more jobs like this?
Get jobs that are Remote delivered to your inbox every week.

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.
Date Posted
01/13/2025
Views
0
Similar Jobs
Senior Specialist Senior Accountant Shared Financial Services - Make-A-Wish America
Views in the last 30 days - 0
The text describes Make a Wish Foundations mission to grant childrens wishes and their community efforts It outlines job positions with remotehybrid o...
View DetailsSenior Design Manager (Infrastructure) - Canonical
Views in the last 30 days - 0
Canonical a leading opensource provider seeks a Senior Design Manager to drive innovation in cloud and AI technologies The role offers remote work glo...
View DetailsSenior Product Designer - Org & Security - Typeform
Views in the last 30 days - 0
This job description outlines a role in developing an intelligent contact management system with AI capabilities The position involves designing user ...
View DetailsExecutive Director Patient Advocacy - Kyverna Therapeutics
Views in the last 30 days - 0
Kyverna Therapeutics is seeking an Executive Director for Patient Advocacy to lead initiatives in autoimmune disease treatment The role involves build...
View DetailsMedical Affairs Writer Contract - Kyverna Therapeutics
Views in the last 30 days - 0
Kyverna Therapeutics seeks a Medical Affairs Writer to develop scientific publications and communications for cell therapy innovations The role requir...
View DetailsProduct Manager Wallet SDKs - Startale
Views in the last 30 days - 0
The text describes a job alert system where applicants must mention UNSELFISH and use a specific tag to demonstrate they read the post It explains the...
View Details