At Thermo Fisher Scientific, we offer meaningful work that makes a positive global impact. Our Clinical Research Services team powers the PPD® clinical research portfolio, helping develop therapies to address the world’s most pressing health challenges. Join us in delivering life-changing results!
Key Responsibilities:
- Provide administrative and technical support to clinical trials.
- Ensure audit readiness by reviewing files per SOPs and guidelines.
- Support rapid site activations through collaboration with project teams and sponsors.
- Conduct reviews of department, internal, country, and investigator files.
- Maintain current, accurate databases (e.g., Activate, eTMF).
- Process regulatory documents and provide system support as needed.
- Assist in scheduling meetings and maintaining vendor trackers.
- Collaborate with the start-up team for regulatory submissions and site document collection.
Qualifications:
- Education: Bachelor’s degree preferred.
- Experience: 6 months to 1 year of relevant experience.
- Skills:
- Strong knowledge of ICH Good Clinical Practices and applicable country regulations.
- Proficiency in MS Office (Word, Excel, PowerPoint) and clinical trial systems.
- Excellent communication skills in English and local languages.
- Ability to work independently or within a team.
- Flexibility to adapt to changing project timelines.
Benefits:
- Competitive remuneration with an annual bonus.
- Comprehensive healthcare and employee benefits.
- Excellent career growth and development prospects within an innovative and inclusive culture.
