Clinical Trial Support Manager at Sanofi, candidates with a BSc in a scientific discipline can apply!
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Clinical Trial Support Manager at Sanofi, candidates with a BSc in a scientific discipline can apply!

Join Sanofi, a global healthcare leader committed to improving lives through innovative medicines and solutions, at our vibrant location in Hyderabad, India. Be an integral part of our mission to make a significant impact on global health, working with a diverse portfolio that spans established treatments and pioneering developments in areas such as immunology and chronic disease care. As a Clinical Trial Support Manager (CTSM), you will play a crucial role in the successful execution and delivery of our clinical studies, contributing your proactive approach and strong organizational skills to a collaborative cross-functional team.

Location: Hyderabad, India

About the Job

As a Clinical Trial Support Manager (CTSM) at Sanofi, you will be pivotal in supporting the end-to-end execution and successful delivery of our clinical studies. Your responsibilities will encompass a wide range of critical activities, including meticulous study documentation mana

gement, effective budget oversight, diligent vendor management, the organization and facilitation of key study team meetings, and the careful monitoring of sample management processes. This role demands a proactive and detail-oriented individual with exceptional organizational capabilities and a proven ability to collaborate seamlessly within a dynamic cross-functional team environment.

Main Responsibilities

  • Ensure the proper creation, maintenance, and availability of all essential study documentation.
  • Develop and actively manage the study budget under the guidance of senior team members.
  • Organize, schedule, and lead effective study-specific meetings, ensuring clear communication and action tracking.
  • Provide crucial support in the management of external vendors involved in the clinical trial process.
  • Diligently monitor and oversee the entire lifecycle of samples, from collection through to analysis.
  • Effectively manage the Investigational Medicinal Product (IMP) throughout the study.
  • Actively participate in Pre-Approval Inspection (PAI) activities to ensure regulatory readiness.

About You

  • Education: Bachelor’s degree in a scientific discipline is essential; an advanced degree is preferred.
  • Experience: A solid understanding of clinical development principles, Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) guidelines, and relevant regulatory requirements within the pharmaceutical industry.
  • Soft Skills & Technical Skills: Exceptional communication, collaboration, and problem-solving abilities are critical for success in this role.
  • Language: Fluency in English, with excellent written and verbal communication skills.

Why Choose Us?

At Sanofi, we foster a supportive and growth-oriented work environment where your contributions are valued, and your career can flourish. We offer comprehensive benefits and the opportunity to be part of a team dedicated to bringing groundbreaking scientific innovations to life, making a tangible difference in the lives of patients worldwide.

CLICK HERE TO APPLY ONLINE

Keywords: Clinical Trial Support Manager, Sanofi, Hyderabad, Clinical Operations, GCP, ICH Guidelines, Pharma Industry

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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