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Clinical Research Lead

3+ years
Not Disclosed
10 Dec. 4, 2024
Job Description
Job Type: Full Time Education: MD 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

Job Title: Clinical Research Lead

Company: Sanofi
Location: India


About Sanofi Business Operations

Sanofi Business Operations, based in India, supports various divisions globally, including Specialty Care, Vaccines, General Medicines, CHC, and R&D. This centralized organization drives efficiency in medical, HEVA, and commercial activities, enabling Sanofi's mission to advance healthcare worldwide.


Main Responsibilities

Strategic Oversight:

  • Develop and implement the Clinical Development Plan (CDP) and provide input for the Integrated Development Plan (IDP).

  • Contribute to defining the product value proposition (TVP), target product profile (TPP), and market access strategy.

Clinical Study Support:

  • Provide medical expertise for clinical studies, including protocol development, informed consent creation, and amendments.

  • Offer training, feasibility analysis, and medical communication support to study teams and stakeholders.

  • Review and ensure the quality and compliance of clinical trial data, case safety events, and centralized monitoring activities.

Regulatory and Safety Compliance:

  • Prepare/review essential regulatory documents like the Investigator Brochure, Clinical Study Report, and Clinical Trial Authorization dossiers.

  • Address queries from Health Authorities, IRBs, and investigators while ensuring adherence to GCP, regulatory standards, and SOPs.

Cross-functional Collaboration:

  • Work with diverse teams, including biostatisticians, medical writers, pharmacovigilance, and regulatory affairs.

  • Collaborate with CROs, steering committees, and other stakeholders to drive successful study execution.

Team Leadership:

  • Mentor clinical scientists and manage team resources.

  • Provide strategic input and decision-making for trial-related challenges, ensuring adherence to timelines and objectives.


Required Qualifications

Education:

  • Medical Doctor (MD)

Experience:

  • Strong background in clinical development with Phase 3 experience preferred.

  • Expertise in clinical trial methodology, protocol development, and regulatory compliance.

  • Proven track record of publishing scientific findings and engaging with the medical community.

Skills:

Scientific & Technical:

  • Deep knowledge of Pulmonary, Allergy, or Immunology, or experience in drug development.

  • Critical evaluation of competitive medical literature and therapeutic area developments.

Soft Skills:

  • Advanced leadership, collaboration, and networking skills in a cross-cultural environment.

  • Strong problem-solving, conflict-resolution, and decision-making abilities.

  • Excellent teaching, presentation, and negotiation skills.

Technical Proficiency:

  • Familiarity with centralized monitoring, data quality assessment, and risk indicators.

  • Open to adopting new digital solutions for operational efficiency.

Language:

  • Fluent in English (written and spoken).


Why Join Sanofi?

Sanofi is committed to creating better outcomes through groundbreaking science and patient-centered solutions. At Sanofi, you will be part of a global team united by a passion for progress, inclusivity, and innovation.

What We Offer:

  • An inclusive work environment valuing diversity and equity.

  • Opportunities to drive meaningful change and contribute to medical advancements.

  • A global platform to grow professionally and personally.

Watch the 'ALL IN' video and explore Sanofi’s Diversity, Equity, and Inclusion initiatives here.

Be part of the extraordinary. Pursue progress with us.