Remote Pharma Clinical Trial Coordinator Job at Thermo Fisher Scientific, Apply Online
Clinical Trial Coord II
Location: Remote, India
Job Id: R-01261580
Job Type: Full time
Category: Clinical Research
Remote: Fully Remote
Work Schedule: Standard (Mon-Fri)
Environmental Conditions: Office
Job Description
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 II. 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 or 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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