Bengaluru Karnataka Medical director, mpmd, pspv Jobs – 268 Open Jobs Today

Medical Director, MPMD, PSPV
Takeda Pharmaceutical —Bengaluru, Karnataka
- Full-time
- Doctoral degree
- Bachelor's degree
- Travel
Director, Shared Services
Terex Corporation —Bengaluru, Karnataka
- Full-time
- Human resources
- Manufacturing
- AI
5d
Director of Product
Serko Ltd —Bengaluru, Karnataka
- ₹75,00,000 - ₹84,00,000 a year
- Full-time
- Hybrid work
- Product management
- APIs
- AI
- Health insurance
Quick apply
Director - Post Merger Integration and Carve Out
Alvarez & Marsal —Bengaluru, Karnataka
- Master's degree
- Project management
- Bachelor's degree
Director of Engineering
Serko Ltd —Bengaluru, Karnataka
- ₹75,00,000 - ₹84,00,000 a year
- Full-time
- Hybrid work
- Computer Science
- Master's degree
- Bachelor's degree
- Health insurance
Quick apply
Department Director
ALSTOM —Bengaluru, Karnataka
- Full-time
- Engineering
- Master's degree
- AI
Senior Medical Reviewer
AstraZeneca —Bengaluru, Karnataka
- Full-time
- Medicine
- Doctoral degree
- Project management
9d
Director, Country Clinical Operations Management
AbbVie —Bengaluru, Karnataka
- Full-time
- Hybrid work
- Customer service
- Analysis skills
- Project management
Director, Support (Bengaluru)
GitLab —Bengaluru, Karnataka
- Full-time
- Remote
- Salesforce
- AI
- Communication skills
- Health insurance
- Paid time off
3d
Assoc Medical Safety Dir
IQVIA —Bengaluru, Karnataka
- Research
- Bachelor's degree
Director/ Senior Director - Operations
Alvarez & Marsal —Bengaluru, Karnataka
- Full-time
- Public speaking
- Master's degree
- Project management
Director, Engineering
Reltio —Bengaluru, Karnataka
- Remote
- Computer Science
- Master's degree
- Analysis skills
- Health insurance
- Cell phone reimbursement
Quick apply
Associate Director-Highways
AECOM —Bengaluru, Karnataka
- Full-time
- Hybrid work
- Engineering
- Master's degree
- Leadership
- Health insurance
- Paid time off
Senior Director - Governance, Risk, & Compliance (GRC)
Unisys —Bengaluru, Karnataka
- Full-time
- Leadership
Senior Director - Authoring
ZS —Bengaluru, Karnataka
- Online application
- Travel
- AI
- Work from home
Director, Business Transformation & Product Management
Palo Alto Networks —Bengaluru, Karnataka
- Full-time
- Master's degree
- Analysis skills
- Bachelor's degree
Senior Delivery Manager / Delivery Lead
Accellor —Bengaluru, Karnataka
- Full-time
- Remote
- Azure
- PMP
- AWS
- Health insurance
- Paid time off
Quick apply
Director - AIG
Alvarez & Marsal —Bengaluru, Karnataka
- Full-time
- Public speaking
- Manufacturing
Director - CFO Services Practice
Alvarez & Marsal —Bengaluru, Karnataka
- Master's degree
- Business development
- Project management
Medical Lead, India
Guardant Health —Bengaluru, Karnataka
- Weekend availability
- Microsoft Powerpoint
- Microsoft Word
- Medicine

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Medical Director, MPMD, PSPV

Takeda Pharmaceutical -
Bengaluru, Karnataka

Apply Now

Job details

Full-time

Qualifications

Doctoral degree
Clinical experience
Quality assurance
Bachelor's degree
EMR systems
AI
Communication skills
FDA regulations

Full job description

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description

Objective:

Provide strategic and medical leadership for global patient safety across assigned products within the MPMD portfolio. Act as the Global Safety Lead (GSL), accountable for end-to-end safety strategy, benefit-risk evaluation, and delivery of high-quality, regulator-ready safety outputs that support development and lifecycle management.

Principal responsibilities include:

Serve as Global Safety Lead (GSL) and the Company-wide subject matter expert in patient for assigned pharmaceutical, biological, drug-device combination products. Accountable for defining and executing the safety strategy and for delivering major safety outputs across the product lifecycle.
Lead PSPV Global Safety Team (GST) and Safety Management Team (SMT), ensuring alignment on safety priorities, timely decision-making, and clear accountability across functions.
Represent the cross-functional program team as a product safety profile and risk mitigation expert for internal (e.g., Takeda Safety Board) and external (e.g., Independent Data Monitoring Committee, regulatory agencies).
Manage cross-functional assessment of benefit-risk profile and ensure consistent, accurate, and timely communication of safety information to internal and external stakeholders.
Provide proactive, science-based guidance on emerging safety issues and risk minimization strategies, ensuring early identification and mitigation of potential risks.

Accountabilities:

Analyze and interpret safety data from various sources including non-clinical, clinical, post-marketing real-world evidence, and scientific literature.
Conduct signal detection, monitoring, evaluation, interpretation, and management, ensuring compliance with global regulatory expectations and internal procedures.
Develop strategy for and lead preparation of responses to safety-related inquiries from regulatory agencies and ethics committees, ensuring responses are scientifically robust, consistent, and inspection-ready.
Ensure communication of all safety information that may impact the benefit-risk profile of assigned products to senior management and governance bodies.
Provide medical safety expertise, medical interpretation, review, and authorship of appropriate sections for critical documents (e.g., protocols and amendments, informed consent forms (ICFs), investigator brochures (IBs), IMPDs, clinical studies reports (CSR), Health Hazard Evaluations (HHE), Signal Evaluation Reports (SER), INDs, NDAs, BLAs, and CTAs) in collaboration with cross-functional colleagues.
Integrate safety considerations into clinical development program for assigned products and development compounds, including input into study design, statistical analysis plans, and key endpoints to ensure appropriate safety characterization.
Manage benefit-risk profile, including authoring and maintaining regulatory documents such as Risk Management Plans (RMPs).
Collaborate and with and influence cross-functional partners, including Clinical Development, Regulatory Affairs, Quality Assurance, Medical Affairs, Marketing, Manufacturing, and Legal, to ensure aligned and consistent safety messaging and decision-making.
Interact with Regulatory Authorities as part of a cross-functional team to support submissions and effectively defend safety positions during regulatory interactions.
Ensure up-to-date representation of safety information in Company Core Data Sheet (including Reference Safety Information) and Investigator Brochure, as well as other labeling documents.
Demonstrate knowledge of regional and global pharmacovigilance regulations and evolving safety expectations.
Support PSPV in maintaining a high-performing, inspection-ready global safety organization, ensuring full compliance with worldwide regulations and internal standards..
Train, mentor, and provide scientific guidance to Pharmacovigilance Physicians and Safety Scientists, helping to build capability and ensure consistency of safety assessments.
Maintain professional knowledge and accreditation by active participation in continuing medical education activities and contribute to a culture of continuous learning and scientific.
Preferred to have capability in leveraging quantitative methodologies and emerging technologies, including artificial intelligence, to enhance signal detection and safety surveillance, while ensuring scientific validity and regulatory acceptability.

Qualifications:

M.D. or D.O. or internationally recognized equivalent, with relevant clinical experience following post-graduate training and appropriate grounding and knowledge of general medicine, epidemiology and biostatistics. Board certification and licensure preferred.
A minimum of 5 years of experience in Drug Safety/Pharmacovigilance, including 3 years in post-marketing safety, with demonstrated expertise in aggregate reporting, safety surveillance, signal management, safety labeling, benefit-risk assessment and risk management is required.
Knowledge and understanding of national and international PV and regulatory guidelines (e.g., FDA, EMA, PMDA, ICH guidelines).
Experience in responding to safety-related inquiries of various regulatory authorities.
Strong scientific judgment and ability to make decisions in the context of uncertainty and incomplete data.
Excellent verbal and written communication skills, with strong interpersonal abilities to effectively engage cross-functional stakeholders and operate in high-visibility, high-stakes governance environments.
Demonstrated ability to influence without authority and drive alignment across global, matrixed teams.

Travel Requirements: Local and international travel across Takeda sites may be required based on business needs.

Work arrangement: Flexible work environment, including hybrid working as per Takeda’s Work policy. Flexibility to support US Eastern Time zone activities may be required occasionally to enable effective global collaboration and urgent regulatory responses.

Locations

IND - Bengaluru

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

Apply Now

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medical director, mpmd, pspv jobs in bengaluru karnataka

Medical Director, MPMD, PSPV

Director, Shared Services

Director of Product

Director - Post Merger Integration and Carve Out

Director of Engineering

Department Director

Senior Medical Reviewer

Director, Country Clinical Operations Management

Director, Support (Bengaluru)

Assoc Medical Safety Dir

Director/ Senior Director - Operations

Director, Engineering

Associate Director-Highways

Senior Director - Governance, Risk, & Compliance (GRC)

Senior Director - Authoring

Director, Business Transformation & Product Management

Senior Delivery Manager / Delivery Lead

Director - AIG

Director - CFO Services Practice

Medical Lead, India

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