Clinical Trial Coord Ii

3 months ago


Remote, India Thermo Fisher Scientific Full time

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Office

**Discover Impactful Work**:
Thermo Fisher Scientific Inc. is seeking a highly motivated individual with a strong work ethic to join our team as a Clinical Trial Coordinator Level I. As a global leader in scientific research, we offer exceptional opportunities to contribute to impactful work on a global scale. In this role, you will be an integral part of our esteemed Clinical Operations team, providing comprehensive support for clinical trials from study start up to monitoring through to study close out. You will have the chance to collaborate with top professionals in the field and play a key role in the successful implementation of clinical programs, ensuring high-quality and cost-efficient clinical studies.

**Responsibilities**:

- Provide administrative and technical support to the Project Team.
- Support audit readiness by ensuring files are reviewed according to the organization's SOP and department guidance document.
- Assist in site activation activities and develop critical path for rapid site activations.
- Collaborate with investigators and site personnel to conduct feasibility assessments.
- Develop and review site lists based on strategic needs and local input.
- Support training of new staff and participate in departmental initiatives for process improvements/enhancements.

**Requirements**:

- Bachelor's degree in life sciences, pharmacy
- Minimum of 2 years of previous experience or a combination of education, training, and related experience.
- Strong organizational skills, attention to detail, and ability to handle multiple tasks efficiently.
- Proven ability to analyze project-specific data/systems for accuracy and efficiency.
- Strong communication abilities and ability to effectively connect with others.
- Proficiency in MS Office (Word, Excel, and PowerPoint) and ability to learn clinical trial database systems.
- Good working knowledge of applicable Country Regulations, ICH Good Clinical Practices, and SOPs for project implementation and execution.



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