Global Medical Development Managers

5+ years

Not Disclosed

India

10 Jan. 16, 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

Job Title: Global Medical Development Manager
Job ID: REQ-10006184
Posted On: 08/01/2025
Location: Telangana, India
Job Type: Full-Time
Employment Type: Regular
Shift Work: No

Job Description

Sandoz is seeking a Global Medical Development Manager to provide leadership in medical development, contribute to clinical study design, and support product development through scientific expertise. This role involves close collaboration with cross-functional teams and external experts to drive product optimization, regulatory compliance, and clinical excellence.

Key Responsibilities:

Analyze pre-clinical findings, drug formulation data, and regulations to support product development.
Engage in the optimization of formulations, medical devices, and medical therapies to improve clinical outcomes and value propositions.
Provide medical expert assessments to support the selection of new product opportunities.
Offer medical input during product development and provide training on medical issues such as indications, pharmacokinetics, and safety.
Collaborate with internal teams, including Regulatory Affairs, Clinical Development, and Commercial Operations.
Contribute to the design of clinical studies and preparation of scientific documents, including Investigator's Brochures and patient consent forms.
Participate in risk management plans and annual safety reports.
Represent Global Medical Development as a subject matter expert and contribute to external partnerships.
Perform Medical Monitoring for clinical studies and resolve development issues affecting patient safety.
Manage medical writing for registration purposes, including the preparation of clinical documentation for new submissions and life cycle management.
Participate in the Sandoz Study Board and collaborate on post-marketing studies and research.
Contribute to continuous improvement initiatives and stay updated with industry trends.

What You’ll Bring to the Role:

Education:

Academic degree in medicine, pharmacy, or life sciences.

Experience:

5+ years of experience in Product Development within the pharmaceutical industry.
Background in medical and clinical development, regulatory affairs, and drug development.
Expertise in clinical trial design and methodology, with a solid understanding of regulatory environments.
Experience in collaborating with regulatory authorities and reviewing scientific literature.
Strong communication, presentation, and cross-functional team collaboration skills.
Ability to work across different therapeutic areas with a strategic mindset.
Budget management and compliance expertise.
Proactive, solution-oriented approach with strong integrity and quality focus.

Why Sandoz?

Sandoz is a leader in Generic and Biosimilar medicines and is dedicated to improving global access to high-quality medicines. Join Sandoz to shape the future of healthcare and contribute to providing affordable, sustainable medicines to millions of patients worldwide.

Commitment to Diversity & Inclusion
Sandoz is committed to building a diverse and inclusive work environment to better represent the patients and communities it serves.

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Global Medical Development Managers

Job Description

Job Description

What You’ll Bring to the Role:

Why Sandoz?

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