Work in Clinical Trials as A Country Approval Specialist at Thermo
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Country Approval Specialist at Thermo Fisher, Apply online

Are you experienced in study startup, clinical operations, or regulatory affairs? Thermo Fisher Scientific is hiring a Country Approval Specialist for a fully remote position based in India. This role is ideal for professionals looking to ensure efficient clinical trial approvals, maintain regulatory compliance, and contribute to life-saving research projects in a global scientific organization.

About the Company:

Thermo Fisher Scientific is the world leader in serving science, with a mission to enable customers to make the world healthier, cleaner, and safer. With a global team of over 125,000 professionals, the company delivers unparalleled access to technologies, purchasing convenience, and pharmaceutical services through its industry-leading brands and platforms. For those who are passionate about clinical research, regulatory operations, and helping drive innovation in healthcare, Thermo Fisher offers a purpose-driven culture, competitive benefits, and career growth opportunities across the globe.

Job Details: 

Job Title: Country Approval Specialist

Remote Type: Fully Remote

Locations: Remote, India

Time Type: Full-time

Job Requisition ID: R-01321978

Work Schedule: Standard (Mon-Fri)

Environmental Conditions: Office

Job Description

About the Role

Join Thermo Fisher Scientific Inc. as a Country Approval Specialist and play a vital role in the world of research

. Work alongside global professionals to ensure seamless implementation of research projects in India while meeting strict approval standards.

Key Responsibilities

  • Coordinate and manage country-specific approval processes for global clinical trials in India.
  • Ensure compliance with local, national, and international regulations.
  • Collaborate with cross-functional teams for successful project implementation.
  • Strictly adhere to project approval timelines.
  • Prepare and submit necessary documentation for regulatory approvals.
  • Maintain accurate records of approval processes.
  • Customize site contracts and negotiate study budgets with participating sites.

Requirements

  • Proven experience in study startup, clinical operations, or regulatory roles.
  • Strong understanding of Indian regulatory requirements and GCP guidelines.
  • Excellent organizational and communication skills.
  • Attention to detail and ability to adhere to regulatory guidelines.
  • Strong analytical skills and ability to work effectively in teams.

APPLY ONLINE HERE

Keywords: Thermo Fisher Scientific, Country Approval Specialist, Work in Clinical Trials, Remote, India, Full-time, Clinical Trials, Regulatory Requirements, GCP Guidelines

Shekhar
Shekhar Suman is the Co-founder of BioTecNika Info Labs Pvt. Ltd. He is an Entrepreneur, Writer, Public Speaker, and a Motivational Coach. In his career, he has mentored more than 100,000+ students toward success in the Biopharma Industry. He heads the BioTecNika Group, which comprises BioTecNika.com, BioTecNika.org, and Rasayanika.com. An avid reader and listener who is passionate about BioSciences. Today Biotecnika is India's largest Biotech Career portal, with over 5 Million subscribers from academia & Industry. It's ranked among the top 50 websites worldwide in the Biology category.

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