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Job Description
Primary Duties
Lead, design, develop and implement Country / Cluster Medical Brand Plans of an assigned portfolio in a focused disease area/s with multiple products
Provide credible scientific expertise, and drive the scientific exchange needs of Key Opinion Leaders, investigators and other stakeholders in patient care, establishing strong professional relationships with medical societies
Design and implement best-in-class scientific programs with external scientific societies, KOLs, investigators and stakeholders in line Global Medical Affairs and Global Clinical plans
Support MSLs team working in the GI portfolio under a therapeutic area through scientific expertise and implementation of Medical best practices.
Job Function and Descriptio n
% of time – 25%
Lead, design, develop and implement Country / Cluster Medical Brand Plans of an assigned portfolio in a focused disease area/s with GI products
Serve as SME in assigned portfolio and collaborate with Therapy Area Lead and Cross-Functional Team to create & execute Medical Plans
Define specific medical programs and activities (e.g., medical meetings, disease state education, advisory boards) and associated resource requirements/budgets
Define key performance indicators and metrics to track progress against the activity plan
Lead initiatives to optimize patient outcomes and product lifecycle within the GI portfolio.
Drive scientific exchange and insights with Key Opinion Leaders, focusing especially on the West region of India
% of time – 25%
Provide credible scientific expertise, and drive the scientific exchange needs of Key Opinion Leaders, investigators and other stakeholders in patient care, establishing strong professional relationships with medical societies
Develop and maintain “peer-to-peer” scientific relationships with key thought leaders in healthcare, academia and government organizations per KOL plans and as requested by KOLs, including the management of strategic scientific partnerships and scientific exchange
Provide support on scientific content for field medical team to help facilitate interactions with healthcare professionals
Serve presence at external meetings including scientific symposia and cooperative group meetings as SME
% of time – 25%
Design and implement best-in-class scientific programs with external scientific societies, KOLs, investigators and stakeholders in line Global Medical Affairs and Global Clinical plans
Collaborate appropriately with KOLs and Investigators to identify areas of shared scientific interest and advance partnerships per medical plan to improve patient outcomes and provide LCM in assigned portfolio.
Provide medical support to Takeda’s clinical research programs and registries including support for evidence gap analysis and clinical development in collaboration with clinical team
Maintain awareness of and access to internal and external information sources available to support best-in-class scientific exchange, and coordinate high-quality interactions between these resources and external customers
% of time – 10%
Respond effectively to requests for scientific exchange on an assigned product as SME for field medical and sales teams
Coordinate response within defined timeline and quality standards to unsolicited inquiries from HCPs and other stakeholders in collaboration with Medical Information.
Develop appropriate responses to unique inquiries as required, such as the presentation of scientific evidence and medical education
Mentor and train MSL team on fundament disease area knowledge and emerging evidence in assigned portfolio including elevating knowledge of medical literature and critical appraisal of scientific publications
% of time – 15%
Research Collaboration, Support, and Publication Planning:
Facilitate, lead, and manage research projects/studies including Phase IV studies, Real World Data (RWD) generation, and Investigator Initiated Trials (IITs) within the assigned therapy area.
Actively identify and establish need gap analysis on unmet needs related to scientific evidence in GI therapy.
Oversee the review, planning and execution of scientific publications, ensuring high-quality dissemination of research findings.
Responsible for the review of essential documents, including protocols, Case Report Forms (CRFs), Clinical Study Reports (CSRs), and manuscripts
Education and Experience Requirements
MBBS/MD is preferred.
3 years of medical affairs experience in biopharmaceutical medicine in Medical Affairs is preferred
Previous experience in customer-facing roles, team handling, and multiple therapeutic areas, preferred
Locations
IND – Gurgaon
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
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