Associate Project Manager-Registry Study Managemnet

5+ years

Not Disclosed

Hyderabad

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

Here’s the rewritten job description with a unique slug:

Associate Project Manager – Registry Study Management | Hyderabad, India | Permanent | Sanofi

Posted on: Jan. 21, 2025
Closing on: Mar. 26, 2025

About the Job:

Sanofi is seeking an Associate Project Manager – Registry Study Management to join their team in Hyderabad. This role focuses on supporting the operational execution of global rare disease registries. As the Associate Project Manager, you will coordinate with internal and external teams, ensuring the successful execution of registry studies, from project planning to compliance, stakeholder management, and risk mitigation.

Key Responsibilities:

Project Planning & Coordination:
- Regularly review project updates, timelines, and resources.
- Coordinate with international/external teams to ensure effective collaboration.
- Develop dashboards and monitor project metrics.
Stakeholder Management:
- Communicate project progress and resolve issues with internal/external stakeholders.
- Ensure alignment with cross-functional teams, investigators, and regulatory bodies.
Regulatory Compliance:
- Ensure adherence to relevant regulations and compliance standards.
- Manage documentation to meet regulatory requirements.
Risk & Quality Management:
- Identify and manage potential risks, supporting mitigation strategies.
- Support quality assurance measures and manage audits/inspections.
Budget Management:
- Monitor site payments, reconcile budgets, and report financial metrics.
- Track project expenses and maintain relevant financial documents.
Reporting & Documentation:
- Maintain detailed records and prepare regular status reports.
- Support KPI tracking and ad-hoc assignments as needed.

About You:

Experience:
- 5+ years in project management, including 3+ years in clinical research or real-world evidence (RWE) management.
- Strong quantitative, analytical, and problem-solving skills.
Education:
- Degree in a scientific discipline, pharmacy, or related field.
Skills:
- Strong communication, project management, and organizational skills.
- Knowledge of clinical studies, GCP, ICH standards, and regulatory requirements.
- Proficiency in English (written and spoken).
Preferred:
- PM certification.
- Experience with Smart Sheets and global projects.

What We Offer:

At Sanofi, we offer equal opportunities and foster an inclusive environment. Join us to make extraordinary discoveries and progress together.

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Associate Project Manager-Registry Study Managemnet

Job Description

Associate Project Manager – Registry Study Management | Hyderabad, India | Permanent | Sanofi

About the Job:

Key Responsibilities:

About You:

What We Offer:

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