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Team Lead - Registry Site Operations

10+ years
Not Disclosed
10 Feb. 6, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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Team Lead - Registry Site Operations at Sanofi (Hyderabad, India)

Location: Hyderabad, India
Job Type: Permanent, Full-time
Posted On: Jan. 31, 2025
Closing On: Mar. 25, 2025

About the Team:
Sanofi Business Operations (SBO) is an internal resource organization based in India, focusing on centralizing processes to support various global functions, including Specialty Care, Vaccines, General Medicines, CHC, CMO, R&D, Data & Digital. SBO aims to reduce reliance on external service providers while fostering internal expertise to deliver tactical support across Medical, HEVA, and Commercial organizations worldwide.

Main Responsibilities:

As the Team Lead – Registry Site Operations, you will be responsible for overseeing the full project lifecycle, managing a team of 10-15 members. Your key duties will include stakeholder engagement, resource planning, team mentoring, and ensuring that ongoing projects meet agreed timelines and quality standards.

People Management:

  • Mentor and guide the team in Registry Study project management and site management.
  • Oversee day-to-day project activities, address technical glitches, and offer solutions to challenges.
  • Ensure business continuity through effective resource and backup planning.
  • Promote innovation and operational excellence within the team and external partners.
  • Act as the primary point of contact for contracting-related activities.
  • Allocate tasks effectively and share best practices to facilitate continuous improvement.

Project Management:

  • Collaborate with global stakeholders to project future needs and set timelines.
  • Ensure timely delivery of projects while adhering to quality standards.
  • Monitor progress and maintain audit-ready trackers, QC processes, and document repositories.
  • Support the team in resolving issues and ensuring accurate data management.

Process Optimization:

  • Propose and implement automation solutions to enhance project management workflows.
  • Simplify processes for stakeholders and provide real-time updates and outputs.
  • Foster innovation within the team and stay updated on operational excellence techniques.

Stakeholder Collaboration:

  • Support global stakeholders in planning, resource allocation, and business continuity.
  • Identify opportunities for process improvements and risk mitigation.
  • Maintain strong relationships with stakeholders, offering solutions for ongoing challenges.
  • Coordinate with internal and external leaders for regular project, site, and data management reviews.

About You:

  • Experience: 10+ years in global clinical trial management, quality review, project tracking, and people management.
  • Soft Skills: Strong communication, organizational skills, and the ability to meet deadlines while managing multiple stakeholders.
  • Technical Skills: Proficiency in ICH-GCP principles, CTMS, EDC systems, and data management. Familiarity with regulatory requirements and risk assessment for registry projects is essential.
  • Education: Post-graduate degree in Life Sciences, Pharma, or Medicine with over 10 years of relevant experience.
  • Languages: High proficiency in written and spoken English.

Why Sanofi?
Sanofi is dedicated to fostering an inclusive, diverse work environment where all employees can thrive and contribute to advancing better science, better medications, and better outcomes. If you are passionate about making a difference and driving change, Sanofi is the place for you.

Apply today and join us in making extraordinary things happen!