ResponsibilitiesThe Associate Manager will develop with support and supervision, relevant medical affairs content, including abstracts, manuscripts, congress posters/presentations, graphical abstracts, systematic literature reviews, plain language summaries, slide decks, medical education resources, social media, infographics, video, multi-media and other types of external-facing medical content. Responsibilities may include researching, organizing, compiling, interpreting, and quality check of various types of technical and/or medical content. Provide solutions to stakeholders in alignment with manager for all projects and collaborate with other teams to drive these solutions (Graphics, Compliance agency, Statistics teams, etc.).  Ensure execution of all projects within expected timelines while adhering to all quality and compliance requirements for medical content. Ensure training on relevant tools and processes, including new generative AI technology platforms, that ensure efficient and compliant execution of all medical affairs content.  Track the progress of projects and resolve any issues/problems with guidance from manager.  Identify and train to become an expert on one new tool/skill for content creation representing the latest trends in the industry.    Qualification & ExperienceAdvanced scientific degree, (eg, MS, MRes, MPharm, PhD, PharmD, MBBS/MD) 2+ years experience in pharmaceutical medicine, including medical affairs, medical compliance. Proven ability to take ownership of individual work and align with more experienced colleagues on scope, timelines, quality expectations, etc.  Strong interpersonal skills to quickly build rapport and credibility with colleagues and key external stakeholders cross culturally/regionally.  Experience in medical content writing /writing in academic settings/ communications experience within an agency, CRO, Pharma / Biotech Company.  Effective English verbal and written communication with flexibility to be clear, consistent, compliant, and appropriate for a variety of settings  Demonstrated ability to work effectively in a team and understand the applications of technology to medical content development  

ResponsibilitiesYou will be responsible to provide tactical and strategic inputs, and business/technical expertise, to Product Management towards ethical promotion of assigned products, in the operational areas listed.You will be responsible for providing strategic inputs for marketing and brand plans, overseeing the design and execution of medical-marketing programs, and facilitating interactions with healthcare professionals.You will be responsible for developing, reviewing, and approving protocol documents and supporting materials for various clinical projects.You will be responsible to provide useful, timely, accurate, and balanced medical information to internal (sales staff) and external customers.You will be responsible for training the Sales Force on basic sciences/assigned products and pre-launch and launch training for new products.You will be responsible to develop and share expertise in identified medical and/or scientific therapeutic areas.You will be one-point Medical Affairs contact for Customer Relationship Management and operational liaison in various functional domains.You will be responsible forfostering a culture of learning and development and managing the Medical Affairs staff, providing training, guidance, and support across various functional domains.You will be responsible to support the cluster Head Medical Affairs in budgeting, provisioning, and expense control.Qualification & Experience Post-graduate degree in Pharmacology or other Medical specialty/ Graduate degree in MedicineMinimum Work Experience6-10 years of relevant experience in medical affairs handling brand medical strategy with at least 2-3 years in a people management roleSkills & Attributes Technical SkillsBasic knowledge of the pharmaceutical industry, drug discovery, research & development, commercialization, promotion, and applicable policies, procedures, regulations, and guidelines.Expertise in clinical trial design and methodology, and understanding of interfaces, and conduct.Behavioral SkillsCommunication skills, both written and verbal (including medical writing and presentation skills).Interpersonal skills, internal & external networking, and the ability to impact and influence.Analytical skills and reasoning, and sound medical judgment/decision making.

Responsibilities• You will be responsible for the engagement of identified key thought leaders through medical affairs activities, in alignment with the overall strategic plan?• You will be responsible to execution of strategic medical affairs plan including but not limited to medical education, product education, medical evidence generation, advisory boards, pre-license activities and special projects??• You will be a therapeutic area scientific expert, responsible for discussing the scientific data pertaining to products on proactive and reactive basis, patients’ treatment trends and studies in the therapeutic areas in which the Company is?? involved, with defined audience of leading specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other Stakeholders) and to be considered a trusted scientific counterpart?• You will be responsible with therapy area lead to support optimal patient outcomes through communication of data, information, knowledge and insights in support of healthcare professional needs and organizational goals??• You will have to represent the organization in various internal & external scientific platforms??• You will have to gather deep insights on disease trends and treatment patterns from key thought leaders and conveying them back to the therapy lead and commercial teams.??• You will need to proactively conduct disease trend analysis in identified disease segments and contribute effectively to the development of annual Medical Affairs Strategy Plan?• You will be receiving and processing scientific information requests received from physicians?• You will have to ensure that all activities in the region are conducted in alignment to organisation’s COBE (Code of Business Ethics) Policy and compliance guidelines.• You will need to collaborate with thought leaders to conduct therapy specific reviews, meta-analysis, case studies, case series, patient reported outcomes and publish them in reputed journals.• You will be responsible for devising an optimal training plan to ensure the flow of the latest medical developments to the sales and marketing teams.• You will jointly be responsible with the therapy area lead to support optimal patient outcomes through communication of data, information, knowledge, and insights in support of healthcare professional needs and organizational goals.• Representing the organization in various internal and external scientific platforms will be among your responsibilities.• You will be responsible for developing the Medical Affairs strategic plan for identified therapeutic areas and products.• Your ability to convert insights on disease trends and treatment patterns from key thought leaders into viable and formidable strategic plans to shape the therapeutic areas of interest will be vital.• You will be responsible for identifying knowledge gaps, practice gaps, and data gaps and developing strategic medical action plans, including but not limited to medical education, product education, evidence generation, and special projects, will fall under your responsibility.• Collaborating with thought leaders to conduct therapy-specific reviews, meta-analysis, case studies, case series, patient-reported outcomes, and publishing them in reputable journals will be part of your role.• Handling complex questions from healthcare professionals related to GGI products or disease areas to satisfaction will be a key responsibility.• You will be responsible for ensuring that all activities in the therapeutic area are conducted in alignment with Dr. Reddy's COBE (Code of Business Ethics) Policy and compliance guidelines will be essential.• You will be responsible for ensuring that all promotional, physician, and patient education materials are approved within stipulated timelines and in alignment with Dr. Reddy's Promotional Material approval policy.• As a product pipeline champion, you will have the ability to identify unmet needs through active stakeholder interactions and actively contribute to the new product ideation and development of differentiated products. Qualification & Experience• Educational Qualification- MBBS with full time post-graduate qualification of at least 2-years’ duration in any discipline of medicine/ M.B.B.S with M.B.A. from a reputed institute • Minimum work experience- Fresh postgraduate or up to 2 years of experience in Field based Medical Affairs.• Strong academic record with deep knowledge of the therapeutic area, strength in research with knowledge of research methodologies and interpretation of medical data?• Experience with scientific acumen and communication skills in order to be accepted by leading specialists in peer-to-peer relationship?• Experience with complex business environments preferred?• Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards.

ResponsibilitiesPreparation, review and approval of of Standard Operating Procedures (SOPs).Preparation, review and approval of various protocols and reports, including:Confirmatory Batch ProtocolHold Time ProtocolProcess Evaluation (Pre-validation) ProtocolTrial ProtocolProcess Performance Qualification/Validation ProtocolStability ProtocolPreparation of Master Production Records (MPRs) such as:Master Formula Record (MFR)Manufacturing Instructions (MI)Production Order Raw Materials (PORM)Good process knowledge of OSD and semi solids processes.Good Expert in MES - PASIX Design and troubleshooting Designing of Master Batch Records (MBRs) in PASIX, ESP, GMBR, PVL, and PMBR based on MPR/PIS/MPC for new products as well as site transfer products, following SOPs and GMP requirements.Document circulation to cross-functional teams (CFT), follow-up for review, corrections, and approval.Creation and modification of Bill of Materials (BOM) and Recipes in SAP.Follow-up for BOM and Recipe-related tasks for Exhibit, Validation, and Commercial products.Creation of codes in SAP, such as:Coated, Core, Blend, Enteric, Sub Coating and Drug LoadingCreation of reservations in SAP.Inter and intra communication for sending BOM messages to CFTs. Qualification & ExperienceB.Pharm/M.Pharm/M.ScMES Design Exposure good to have

ResponsibilitiesMedical Strategy & PlanningExecute the Medical Affairs plan for DRL new product launch in EM countriesProvide strategic inputs to cross-functional teams including marketing, strategy, regulatory, portfolio and clinical developmentSupport the creation of target patient profiles, CLM contents and contribute to product differentiation strategiesScientific Engagement & CommunicationBuild and maintain relationships with a set of KOLs globally and support country teams (MSL/ commercial) to address HCP queriesOrganize and lead COE-driven scientific events such as advisory boards, global webinars, and ISPsDisseminate scientific updates at internal and external meetings on product and therapy areaEvidence Generation & PublicationsSupport DRL sponsored or investigator initiated studies, real-world evidence generation, and post-marketing surveillance, as and when requiredContribute to scientific publications, conference proceedings, and subsequent development of HCP communication on those studiesOther Core Internal and Administrative SupportReview and approve promotional materials/ events/ FMV calculation/ KOL tiering and ensure compliance with SOPs and regulatory standardsConduct training sessions for internal teams (MSLs/ commercial) on disease area, product knowledge, guidelines, differentiation etc. at regular intervalProvide scientific and clinical support to sales, marketing, portfolio and strategy teamsMarket Insights & Future Strategy DevelopmentGather and analyse customer insights and market trends to further strengthen medical and commercial strategiesEvaluate new products and provide medical rationale for portfolio expansion in related disease areaSupport digital content creation, review, and approval for DRL platforms and leverage technology for scientific exchange and stakeholder engagementQualification & ExperienceMBBS + MD Pharmacology from a recognized medical institute in IndiaMinimum 2 years of experience in Medical Affairs in pharmaceutical industryMust have prior experience in handling products in Diabetes and Cardiovascular therapy areas, preferably launching novel entitiesGood understanding of clinical research, medical statistics, regulatory standards, and therapeutic area expertiseExcellent English communication, presentation skills, and project/stakeholder management skills.

ResponsibilitiesYou will be responsible to provide tactical and strategic inputs, and business/technical expertise, to Product Management towards ethical promotion of assigned products, in the operational areas listed.You will be responsible for providing strategic inputs for marketing and brand plans, overseeing the design and execution of medical-marketing programs, and facilitating interactions with healthcare professionals.You will be responsible for developing, reviewing, and approving protocol documents and supporting materials for various clinical projects.You will be responsible to provide useful, timely, accurate, and balanced medical information to internal (sales staff) and external customers.You will be responsible for training the Sales Force on basic sciences/assigned products and pre-launch and launch training for new products.You will be responsible to develop and share expertise in identified medical and/or scientific therapeutic areas.You will be one-point Medical Affairs contact for Customer Relationship Management and operational liaison in various functional domains.You will be responsible forfostering a culture of learning and development and managing the Medical Affairs staff, providing training, guidance, and support across various functional domains.You will be responsible to support the cluster Head Medical Affairs in budgeting, provisioning, and expense control.Qualification & ExperienceEducational QualificationPost-graduate degree in Pharmacology or other Medical specialty/ Graduate degree in MedicineMinimum Work Experience6-10 years of relevant experience in medical affairs handling brand medical strategy with at least 2-3 years in a people management roleBasic knowledge of the pharmaceutical industry, drug discovery, research & development, commercialization, promotion, and applicable policies, procedures, regulations, and guidelines.Expertise in clinical trial design and methodology, and understanding of interfaces, and conduct.Communication skills, both written and verbal (including medical writing and presentation skills).Interpersonal skills, internal & external networking, and the ability to impact and influence.Analytical skills and reasoning, and sound medical judgment/decision making.

Responsibilities• You will be responsible for the engagement of identified key thought leaders through medical affairs activities, in alignment with the overall strategic plan?• You will be responsible to execution of strategic medical affairs plan including but not limited to medical education, product education, medical evidence generation, advisory boards, pre-license activities and special projects??• You will be a therapeutic area scientific expert, responsible for discussing the scientific data pertaining to products on proactive and reactive basis, patients’ treatment trends and studies in the therapeutic areas in which the Company is?? involved, with defined audience of leading specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other Stakeholders) and to be considered a trusted scientific counterpart?• You will be responsible with therapy area lead to support optimal patient outcomes through communication of data, information, knowledge and insights in support of healthcare professional needs and organizational goals??• You will have to represent the organization in various internal & external scientific platforms??• You will have to gather deep insights on disease trends and treatment patterns from key thought leaders and conveying them back to the therapy lead and commercial teams.??• You will need to proactively conduct disease trend analysis in identified disease segments and contribute effectively to the development of annual Medical Affairs Strategy Plan?• You will be receiving and processing scientific information requests received from physicians?• You will have to ensure that all activities in the region are conducted in alignment to organisation’s COBE (Code of Business Ethics) Policy and compliance guidelines.• You will need to collaborate with thought leaders to conduct therapy specific reviews, meta-analysis, case studies, case series, patient reported outcomes and publish them in reputed journals.• You will be responsible for devising an optimal training plan to ensure the flow of the latest medical developments to the sales and marketing teams.• You will jointly be responsible with the therapy area lead to support optimal patient outcomes through communication of data, information, knowledge, and insights in support of healthcare professional needs and organizational goals.• Representing the organization in various internal and external scientific platforms will be among your responsibilities.• You will be responsible for developing the Medical Affairs strategic plan for identified therapeutic areas and products.• Your ability to convert insights on disease trends and treatment patterns from key thought leaders into viable and formidable strategic plans to shape the therapeutic areas of interest will be vital.• You will be responsible for identifying knowledge gaps, practice gaps, and data gaps and developing strategic medical action plans, including but not limited to medical education, product education, evidence generation, and special projects, will fall under your responsibility.• Collaborating with thought leaders to conduct therapy-specific reviews, meta-analysis, case studies, case series, patient-reported outcomes, and publishing them in reputable journals will be part of your role.• Handling complex questions from healthcare professionals related to GGI products or disease areas to satisfaction will be a key responsibility.• You will be responsible for ensuring that all activities in the therapeutic area are conducted in alignment with Dr. Reddy's COBE (Code of Business Ethics) Policy and compliance guidelines will be essential.• You will be responsible for ensuring that all promotional, physician, and patient education materials are approved within stipulated timelines and in alignment with Dr. Reddy's Promotional Material approval policy.• As a product pipeline champion, you will have the ability to identify unmet needs through active stakeholder interactions and actively contribute to the new product ideation and development of differentiated productsQualification & Experience• Educational Qualification- MBBS with full time post-graduate qualification of at least 2-years’ duration in any discipline of medicine/ M.B.B.S with M.B.A. from a reputed institute • Minimum work experience- Fresh postgraduate or up to 2 years of experience in Field based Medical Affairs.• Strong academic record with deep knowledge of the therapeutic area, strength in research with knowledge of research methodologies and interpretation of medical data?• Experience with scientific acumen and communication skills in order to be accepted by leading specialists in peer-to-peer relationship?• Experience with complex business environments preferred?• Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards.

ResponsibilitiesDrive new product launch excellence and medical execution for priority oncology and haematology brands across Emerging Markets (EM) for Dr. Reddy’s Laboratories (DRL). Provide strategic growth levers and scientific insight for new and existing key products by translating clinical and real-world evidence into clear value narratives and practical field/commercial application. Enable high-impact scientific engagement (international speaker programs/ISP-CME, webinars, advisory boards, and in-country KOL visits) to strengthen scientific exchange and evidence utilization. Provide guidance and enablement to country teams for RWE generation and pharmacoeconomic/HEOR planning to support market access readiness. Ensure compliant execution through timely approvals and governance for scientific/promotional materials and external engagements in line with internal processes and applicable regulations.Provide guidance, governance and decision support to country medical teams for RWE generation, and pharmacoeconomic/HEOR planning. Support development of country-specific medical plans, study concepts, and evidence roadmaps to strengthen payer, access, and clinical value narratives.Ensure timely, high-quality compliance reviews and approvals for scientific/promotional materials and external engagements (e.g., ISP/CME, webinars, advisory boards, speaker nominations, FMV inputs, HCP classification/eligibility) in line with internal processes and applicable regulations. Qualification & ExperienceMBBS and MD with Pharmacology or Medicine with overall experience of ?3 years in medico-marketing function, preferably with exposure to oncology/haematology Past experience of conducting KOL interactions/ Advisory Board meetings/ CMEs with thought leaders Experience of real-world clinical studies is desirable In-depth understanding about various cancers and principles of cancer therapy including latest products as well as upcoming treatment options and therapy modalities

ResponsibilitiesYou will be responsible to foster relationships with key opinion leaders and doctors, gathering feedback and competitor information, while providing medical support through Continuing Medical Education (CME) and resolving queries. Collaborate with the project management team to organize Sparsh and life awareness programs, nurturing positive connections with stakeholders. You will be responsible of weekly goal setting for each product and each doctor, study market trend and competitors’ products to understand their influence on customers in order to ensure that goals set for each week are achieved and overall yearly sales targets are met. You will be responsible to coordinate field activities for Continuing Medical Education (CME) programs, persuading doctors to participate with the company.Arrange speakers and venues for CME events, collaborating with other divisions to jointly organize the sessions. You will be responsible to manage logistics for corporate social responsibility initiatives like the awareness for Life program, contributing to the establishment of the company's brand image within the medical community. You will be responsible to review the sales of existing products through weekly sales review meetings, weekly statements from stockiest and compare against set targets, take corrective actions in case of any shortfalls to ensure that weekly sales targets are achieved. You will be responsible to manage Territory Data by regularly engaging with pharmacy managers and distributors to collect sales data and input RCPA data into the Unnati portal. You will be responsible to maintain an updated list of doctors within the designated area via handheld devices, and regularly meet with retailers to track product status. You will be responsible to organize monthly schedules using palm-top devices, inputting visit data and generating reports as necessary to ensure the portal contains the latest information. Qualification & Experience B.Pharma Minimum work experience- 2 years of experience in Oncology preferably in that region.

Responsibilities  MI Operations Leadership – U.S. Focus and also Global Flexibility - End?to?end U.S. MI operations run per MI Control Docs and GMI SOPs; compliant, balanced, timely responses; documented separation of promotional/non?promotional; flexible support to other regions as assigned.  Content Governance & Change Control U.S. SRDs/FAQs and digital MI content aligned to current U.S. PI and evidence standards; controlled updates for label/safety changes; complete audit trails in repository; periodic content quality reviews passed.  Inquiry Handling Oversight, Documentation & Privacy Unsolicited, non?promotional fulfillment; accurate verbatim capture; documentation completeness; adherence to privacy expectations (incl. HIPAA?aligned handling where applicable); periodic QC shows ?95% documentation accuracy.  Assist GMI Head/ Designee in miscellaneous activities and projects as assigned Effective support for strategic and operational initiatives; tasks completed within agreed timelines  PV & Product Quality Integration Reliable intake and on?time routing of AEs/special situations and PQCs to PV/QA per SOPs and regulatory timelines; reconciliations completed; zero critical PV/QA findings linked to MI channels.  Vendor/Partner Management & QMS Alignment