Job Description

Work Schedule Standard (Mon-Fri)
Environmental Conditions Office

What makes this opportunity outstanding
At Thermo Fisher Scientific, we offer you an outstanding opportunity to be part of a world-class team that is driven by innovation and collaboration. You'll have the chance to work on groundbreaking projects and contribute to research that makes a real difference. Our dedication to excellence ensures that you will thrive in a dynamic and inclusive environment where your ideas are valued and your career can flourish!
Responsibilities

• Coordinate and lead all aspects of clinical trials to ensure data integrity and compliance with regulatory requirements.
• Collaborate with cross-functional teams to successfully implement study protocols and achieve project achievements.
• Monitor and report on the progress of clinical research projects, ensuring timely completion of deliverables.
• Maintain accurate and comprehensive documentation of all research activities.
• Strictly adhere to industry standards and company guidelines to achieve flawless execution of clinical studies.

Requirements

• Proven experience in clinical research, specifically in a on-site monitoring role for minimum of 3 years
• Strong understanding of Indian regulatory requirements and Good Clinical Practices (GCP).
• Outstanding organizational and time management skills to manage multiple projects effectively.
• Ability to determine priorities and compete tasks under tight deadlines.
• Excellent communication and interpersonal skills to collaborate with diverse teams.
• Ambitious and motivated to contribute to the success of our research initiatives.
• Willing to be based in a major metro city (Mumbai, Delhi NCR, Bengaluru, Hyderabad, Ahmedabad)

Join us
If you are passionate about advancing science and making a positive impact, we invite you to join our team at Thermo Fisher Scientific. Together, we can achieve outstanding outcomes and drive scientific innovation to new heights.

Skills Required