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Clinical Project Lead

5+ years
Not Disclosed
10 Feb. 17, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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 Project Lead

Location: Hyderabad, India
Job Type: Permanent, Full-time
Posted On: January 31, 2025
Expiration Date: March 27, 2025


Hiring Manager:

Project Lead – ESR and Grants

Travel Requirement:

Travel required based on business needs


About the Job:

Sanofi Business Operations (SBO) is an internal Sanofi resource organization, set up to centralize processes and activities supporting various functions within Sanofi globally, including Specialty Care, Vaccines, General Medicines, CHC, CMO, R&D, Data & Digital. SBO strives to become a strategic and functional partner to medical, HEVA, and commercial teams, and works toward reducing reliance on external service providers by developing internal expertise.


Main Responsibilities:

Feasibility Activities:

  • Assist in country and site selection processes in collaboration with Registries Team and Local Medical Affairs.

Study Start-up Activities:

  • Arrange necessary registry materials such as protocols, Case Report Forms (CRFs), Protocol Agreement Forms (PAFs), etc., for ethical and regulatory submissions.

  • Ensure financial contracts are executed for each site and assist in the contracting process.

Project Management:

  • Oversee all registries within assigned countries.

  • Maintain status updates on registries for the Global Registries Team.

  • Coordinate with Clinical Research Associates.

  • Monitor data quality and prepare project tracking and reporting systems.

  • Monitor contract issues and arrange payments in accordance with agreed-upon milestones.

  • Liaise with Medical Affairs Teams for applicable topics.

Safety & Quality:

  • Ensure proper safety reporting processes according to country regulations and SOPs.

  • Maintain an audit/inspection readiness mindset, addressing issues and deviations through Corrective and Preventive Actions (CAPA) when necessary.

Study Administration:

  • Train new Clinical Research Associates (CRAs) and additional temporary resources.

  • Maintain study tables, trackers, and databases, ensuring compliance with eTMF processes throughout the study.

  • Participate in study team meetings and international investigator meetings (as required).

People and Performance:

  • Align with internal and external stakeholders to prioritize registry study activities.

  • Support team initiatives and recommend process improvements.

  • Ensure compliance with regulatory requirements, including ICH/GCP guidelines.

  • Address and resolve issues during registry execution using strong problem-solving skills.

Stakeholder Communication:

  • Ensure effective communication with internal and external stakeholders, providing regular updates and addressing concerns.

  • Actively involve stakeholders in project planning and decision-making processes.


Experience and Qualifications:

Experience:

  • Minimum of 5 years of experience in clinical research & development, with at least 2 years in clinical trial project management.

  • Experience in working on global projects in an international matrix environment.

  • Project management certification is preferred.

  • Strong quantitative, analytical, and problem-solving skills.

Skills:

  • Soft Skills: Excellent written and oral communication, organizational skills, cross-functional collaboration, and stakeholder management.

  • Technical Skills:

    • Familiarity with ICH-GCP principles and local regulatory requirements.

    • Proficiency in CTMS and EDC systems.

    • Knowledge of FDA regulations and ICH/GCP guidelines.

    • Experience in data management, including data cleaning and validation.

    • Ability to mitigate risks associated with registries to ensure smooth project execution.

Education:

  • Degree in Pharma/scientific discipline or related Life Science degree.

  • Substantial project management or clinical trial experience in drug development.