Company

GlobalMedicalManager,Gastro

Mumbai, Maharashtra, India FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“Global Medical Manager, Gastro. Skills: medical affairs strategy, KOL management, scientific liaison. Supports Global Medical Director. Provides scientific / medical liaison”

Industry & Context.

Eligibility Requirements

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)

What They're Looking For.

Must Have

minimum 5 years’ experience in the relevant field of the pharmaceutical industry, minimum of 7 years’ experience in the relevant field of the pharmaceutical industry, minimum of 5 years’ experience in the relevant field of the pharmaceutical industry, Good understanding and experience in conduct of clinical trials or in medical research in the pharmaceutical industry or academia or equivalent, Knowledge of clinical / medical trial methodology, oversight/evaluation of safety and regulatory requirements governing clinical / medical trials, experience in KOL management and scientific society relations are required, understanding of compliance requirements, English proficiency (oral and written)

Nice to Have

Prior experience in country/regional medical role is desirable, other languages considered an advantage

What You'll Do.

Supports Global Medical Director

Provides scientific / medical liaison

Drives and generates innovative medical ideas

Identifies suitable mid- and long-term differentiating opportunities

Continuous medical evaluation of products

Provides sound and up-to-dated medical information

Prepares therapeutic area target product profiles

Drives medical scientific knowledge

Drives TA medical plans

Responsible for global medical affairs research projects

Secures and maintains good collaboration

Drives & oversees establishment and maintenance of scientific collaborative relationships

Oversees TA medical content generation

Initiates and leads medical affairs activities

Leads safety monitoring

Provides medical evaluation and propose scientific strategies

Develops and maintains proper and up to date product and disease state trainings

Oversees medical expert opinion

Supports the process of product-specific medical queries

Safeguards that marketing activities are done in compliance

How You'll Work.

Team & Collaboration

Provides scientific / medical liaison to internal stakeholders; Prepares therapeutic area target product profiles (TPP) with a cross-functional team; Supports internal cross-functional teams (brand teams, project teams, product safety team, labeling sub-team); Provides scientific liaison to these teams; Ascertains a proper alignment of medical, I&D and marketing activities; Secures and maintains good collaboration with the regional and local medical directors; As a member of the scientific review and approval board; As a member of the Product Safety Team

Communication Scope

written and verbal communication skills; presentation skills

Full Job Description

## **JOB DESCRIPTION:** **Primary Job Function:** * Supports Global Medical Director to define medical affairs strategy and medical activities related to GI&H TA. **Core Job Responsibilities:** * Supports and conducts following responsibilities under supervision of Global Medical Director * Provides scientific / medical liaison to internal stakeholders. * Drives and generates innovative medical ideas regarding potential new development opportunities in the respective therapeutic area based on key insights and perspectives from multiple stakeholders. * Identifies suitable mid-and long-term differentiating opportunities with a potential of meeting unmet current medical needs. * Continuous medical evaluation of products under scope of responsibility, identifying potential substances to fill gaps in portfolio (including in-licensing opportunities to fully address patients’ needs based on latest scientific knowledge) * Provides sound and up-to-dated medical information, disease knowledge and medical training to stakeholders such as e.g. I&D departments, Public Affairs, Marketing/Commercial departments, affiliate (medical) teams * Prepares therapeutic area target product profiles (TPP) with a cross-functional team. * Drives medical scientific knowledge, evaluates, and reviews medical literature, generates potential new differentiated ideas (incl. digital) to enhance and maximize potential benefit for disease management and patient care. * Drives TA medical plans, incorporating therapeutic area strategy, areas of research interests, publication planning, tactical plans, study initiatives. * Responsible for global medical affairs research projects, and reviews and jointly approves all medical research activities that are primarily led by the medical affairs as a member of the scientific review and approval board. * Secures and maintains good collaboration with the regional and local medical directors for alignment of local activities with the global brand strategies. * Driv

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