15 Medical Information Jobs

Role Overview: You will be responsible for leading and managing the MI&E team(s) in the NoCC Site to ensure the delivery of high-quality, scientifically accurate, compliant, and timely responses to requests for information from Healthcare Professionals (HCPs). Key Responsibilities: - Co-lead the development and implementation of standards to ensure quality, accuracy, and compliance with industry standards and practice codes in collaboration with USMA Medical Information and Engagement Leadership. - Act as the designated business contact for MI&E systems in alignment with the USMA MI&E team. - Maintain quality and consistency of responses to Medical Response Documents (MRDs) and handle any re...

**Job Description** **Role Overview:** As a Medical Manager for Rare Blood Disorder at Sanofi, you will be responsible for executing the Medical and scientific strategy for the SE Asia & India MCO portfolio in alignment with the franchise strategy. Your role will involve being a strategic, solution-oriented, and flexible individual who can build strong relationships with key external experts and stakeholders. **Key Responsibilities:** - Act as a trusted scientific partner to external experts by conducting timely scientific exchanges to enhance understanding of product value - Develop and share medical insights to contribute to key medical messages - Keep abreast of medical developments to id...

Role Overview: As the Medical Safety Lead at Sandoz, you will be responsible for owning the safety strategy of assigned products and ensuring ongoing evaluation of the overall safety profile. You will serve as the medical safety representative for various safety documents and assessments, including Risk Management Plans, Periodic Safety Update Reports, and medical risk assessments. Additionally, you will collaborate with internal and external stakeholders to support safety-related activities and submissions. Key Responsibilities: - Own the safety strategy of assigned products and evaluate the overall safety profile - Serve as the medical safety representative for Risk Management Plans, Perio...

Role Overview: As an Associate Director Medical Information Group Lead at Novartis, you will be accountable for managing and leading a Medical Information delivery team to produce high-quality medical information documents and responses. You will play a key role in driving functional excellence, stakeholder management, and ensuring compliance with all relevant internal SOPs/guidelines and external regulatory requirements. Key Responsibilities: - Responsible for the performance of the assigned Medical Information team to deliver as designed with quality, timeliness, and in a compliant manner. - Track progress, identify improvement opportunities, and share best practices across the Medical Inf...

As a Medical Information Specialist at VIATRIS, your role is crucial in providing technical and scientific support for responding to unsolicited inquiries. Your responsibilities include researching, creating, and updating Global Scientific Response Documents (GSRDs) to ensure accurate and timely responses to medical inquiries. You will also manage escalated inquiries, peer review colleagues" work, provide literature services, and participate in global medical information projects. Key Responsibilities: - Create, maintain, and review GSRDs and related content to provide medically and scientifically accurate responses - Develop comprehensive knowledge of Medical Information (MI) work processes...

Overview CACTUS is a remote-first organization, and we embrace an accelerate from anywhere culture. You may be required to travel to our Mumbai office based on business requirements or for company/team events. If you are looking for challenging and rewarding work which combines your understanding of medical science and aptitude for writing into one unique job, the Senior Manager, Scientific Communications role is for you. This is an opportunity to grow your career and make a greater impact on the lives around you. Responsibilities Leading and taking ownership and responsibility for development (write, review, proofread, and data-check) of high-quality, client-ready scientific, medical, and e...

Summary In close collaboration with the Global Program Safety Lead (GPSL) provides robust safety evaluation expertise and medical innovation in order to improve patients lives and impact on overall Novartis results. As a member of the Medical Safety organization, prioritizes the safety of patients, ensures optimal patient safety for assigned compounds and shares responsibility for the integration, analysis, and evaluation of internal and external safety information through product lifecycle management, and evaluation of internal and external safety information through product lifecycle management About The Role Key Responsibilities Monitors the clinical safety of projects/products including ...

As a Medical Science Liaison Oncology with a Global Pharma MNC, your role will involve building and strengthening the medical affairs presence in oncology by engaging key stakeholders, supporting research, and sharing scientific insights on hard-to-treat cancers. This field-based position will primarily cover India. **Key Responsibilities:** - Engage with Key Opinion Leaders (KOLs), hospitals, and institutions to provide fair and balanced medical information. - Support company-sponsored studies, Investigator-Initiated Trials (IITs), registries, and Real-World Evidence (RWE) projects. - Offer medical expertise and field insights to internal teams. - Collaborate with sales, market access, and ...

Role Overview: You will be responsible for providing medical expertise and support to the Sales Force for Pharma, vaccines, and Nutrition. This includes offering expert medical and scientific input to both internal and external stakeholders, staying updated on the latest scientific literature and clinical developments, responding to medical inquiries from healthcare professionals, patients, and internal teams, as well as developing and maintaining medical information resources. Key Responsibilities: - Identify, develop, and maintain relationships with Key Opinion Leaders (KOLs). - Organize and participate in advisory boards, speaker programs, and other medical education activities. - Gather ...

The Medical Representative is responsible for promoting and selling the pharmaceutical products of the company to healthcare professionals such as doctors, pharmacists, and hospitals. You will work towards increasing product awareness, addressing queries, and providing guidance on product usage while meeting sales targets in the assigned territory. Your key responsibilities include achieving monthly, quarterly, and annual sales targets by promoting and selling pharmaceutical products to healthcare professionals. Building and maintaining strong relationships with doctors, pharmacists, and other stakeholders is essential. You will provide accurate information about the products, communicate pr...

As a Medical Advisor at our company, you will play a crucial role in supporting medical affairs through your scientific and clinical expertise. Your responsibilities will include providing scientific and clinical input to various teams, responding to medical queries, conducting literature reviews, developing training materials, engaging with Key Opinion Leaders, ensuring compliance with guidelines, and maintaining accurate records. You will be expected to collaborate effectively with cross-functional teams such as marketing, sales, and regulatory, ensuring the accuracy and compliance of promotional materials. Additionally, you will be responsible for responding to medical queries from intern...

As a medical data analyst, you will utilize data analytics to enhance healthcare outcomes. Your primary responsibilities will include gathering, analyzing, and interpreting medical information to support medical facilities in enhancing patient care, increasing efficiency, and reducing costs. This is a full-time position with benefits such as health insurance, leave encashment, and provident fund. The working hours are during the day shift, and the role requires you to work in person at the designated work location.,

As a Medical Affairs professional at Pfizer, your role involves providing scientific expertise and building relationships with Key Opinion Leaders to advance medical practice and research for the benefit of society. By actively contributing to the organization, you will take responsibility for ensuring the scientific, technical, and ethical soundness of all policies, statements, and endeavors. Your focus will be on delivering high-quality and timely service in various areas such as Interactions with Healthcare Professionals, Continuing Medical Education, Clinical Research, Sales Force Training, and support for New Product Development, Regulatory Affairs, Quality Standards, and Business Techn...

As a Clinical Evaluation Medical Writer at Medtronic, you will play a crucial role in developing and updating clinical evaluation documents to support CE Mark submissions and ensure compliance throughout the product lifecycle. Your work will involve close collaboration with cross-functional teams to gather and interpret data on device safety, performance, and benefit-risk according to MEDDEV 2.7/1 Rev. 4 and EU Regulation 2017/745. You will also be responsible for summarizing and disseminating clinical literature and other available data to share relevant evidence, while managing Medical Information activities. This includes tracking inquiries, monitoring key metrics, researching and respond...

As a Medico-Marketing Writer at Remedium, a healthcare strategy consulting firm in India, you will be responsible for creating accurate, engaging, and scientifically sound content tailored for healthcare professionals (HCPs), patients, and internal stakeholders. Your primary focus will be on developing scientific content that adheres to clinical evidence, therapy guidelines, product positioning, and brand strategy. In addition to scientific content development, you will be involved in end-to-end asset creation for below-the-line (BTL) and above-the-line (ATL) materials. This includes creating a variety of materials such as brochures, product dossiers, interactive visual aids, detailing aids,...