6 Medical Information Jobs

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 product features effectively, and participate in promotional activities like doctor meetings and CMEs. Additionally, you will be responsible for gathering market intelligence on competitor products and market trends, providing feedback to the marketing team, and identifying new opportunities for product growth. Planning and executing daily call schedules, ensuring effective territory coverage, and maintaining accurate records of customer interactions are crucial for success in this role. Compliance with company policies, industry regulations, and ethical standards is mandatory. You will need to maintain detailed records of all interactions with healthcare professionals and submit regular reports on sales activities, product promotion efforts, and territory performance to the Area Sales Manager. Key Skills & Qualifications: - Education: Bachelors degree in pharmacy, life sciences, or related field. - Experience: 1-3 years of experience in pharmaceutical sales preferred. - 2+ years" experience in Cardio Diabetic/Respiratory Segments. - Skills required include excellent communication and interpersonal skills, strong sales and negotiation abilities, clear explanation of complex medical information, self-motivation, target-driven mindset, and good organizational and time management skills. No of openings: - Cochin: 2 - Kottayam: 1 - Kollam: 1 - Trivandrum: 2 - Calicut: 2 - Kannur: 1 - Malappuram: 1 - Thrissur: 2,

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 internal stakeholders and healthcare professionals, as well as preparing and organizing scientific data and clinical information. Your role will also involve conducting thorough literature reviews to support discussions on product positioning, safety, and efficacy. You will analyze clinical data to derive insights relevant to therapy areas, contributing to the advancement of healthcare solutions. Furthermore, you will assist in developing and delivering training materials, staying updated on the latest developments in assigned therapeutic areas, and engaging with Key Opinion Leaders through advisory board meetings and Continuing Medical Education activities. To excel in this role, you should hold MBBS and MD degrees in Pharmacology, with a solid understanding of clinical pharmacology and therapeutic areas. Strong communication and presentation skills are essential, along with the ability to work collaboratively in a cross-functional environment. Attention to detail, a strong analytical mindset, and knowledge of regulatory and ethical guidelines in medical affairs would be advantageous. If you are a motivated and detail-oriented individual who has recently completed their MBBS and MD in Pharmacology, this opportunity offers a great start to your career in medical affairs. Join us to contribute to the pharmaceutical industry, engage with healthcare professionals, and make a difference in advancing healthcare solutions.,

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 Technology. You will serve as a critical interface with identified scientific leaders, building regional, national, or international relationships to enhance understanding of diseases, research trends, clinical practice guidelines, and treatment patterns relevant to Pfizer's business objectives. With support from mentors or Line managers, you will provide tactical and strategic inputs to Product Management for the ethical promotion of assigned products. Your operational responsibilities will include engaging with Key Opinion Leaders and organizations in alignment with medical affairs colleagues to support medical activities related to brand plan strategies. This involves developing presentations tailored to specific programs/regional requests, obtaining approval from Medical Advisors before rollout, and establishing relationships with key opinion leaders/organizations for collaborative clinical and research activities in select therapeutic areas. You will participate in promotional and educational interactions with Health Care Professionals, focusing on stage shifting for Key Opinion Leaders as per business unit objectives. Additionally, you will support efforts to identify new investigators and institutions for Clinical Research, provide medical support for local studies, and assist in the development and execution of publication plans. Medical Initiatives will involve participating in key opinion leader meetings, advisory boards, Customer Launch Meetings, round table discussions, and conducting Continuing Medical Education activities as required. Ensuring the provision of useful, timely, accurate, and balanced medical information to internal and external customers is a key aspect of this role, in adherence to relevant SOPs and policies. Pfizer is an equal opportunity employer, complying with all applicable equal employment opportunity legislation in each jurisdiction of operation. Join us in our mission to make a positive impact on healthcare practices and research, while enhancing Pfizer's reputation in the scientific community.,

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 responding to technical and clinical questions from internal teams and external healthcare professionals under the guidance of Clinical and Medical Affairs. Success in this role will require strong skills in scientific writing, literature review, data analysis, and clear communication, as well as a proactive and collaborative mindset. Your responsibilities may include independently creating and maintaining clinical evaluation documents in compliance with relevant regulations and company procedures, supporting Medical Information activities by responding to inquiries, conducting literature searches and reviews, reviewing scientific materials for accuracy and compliance, developing reports, identifying and reporting complaints or adverse events, and collaborating with key stakeholders to drive evidence-based scientific decisions. To excel in this position, you are required to have a mastery of a specialty area and full knowledge of industry practices, typically obtained through advanced education combined with experience. A Baccalaureate degree and a total of 8 years of experience with a minimum of 4 years of relevant experience, or an advanced degree with a minimum of 2 years of relevant experience are also required. Medtronic offers a competitive salary and flexible benefits package as part of its commitment to employees. The company values the contributions of its employees and offers various benefits, resources, and competitive compensation plans designed to support you at every career and life stage. The position is also eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). Medtronic is a global leader in healthcare technology that aims to address the most challenging health problems facing humanity by seeking out innovative solutions. With a mission to alleviate pain, restore health, and extend life, Medtronic unites a global team of passionate individuals who are committed to making a difference. The company values diversity and is dedicated to engineering extraordinary solutions for real people by leveraging talent, diverse perspectives, and ambitious ideas. To learn more about Medtronic's business, mission, and commitment to diversity, please visit their website.,

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, social media posts, and more. For ATL materials, you will support with messaging and claims for advertisements while ensuring scientific compliance and clarity. Your role will also involve providing regulatory and medical review support to ensure all content meets medical, legal, and regulatory standards. You will collaborate with medical, legal, and regulatory (MLR) teams to address feedback and finalize compliant material. As part of the collaboration and project management aspect of the role, you will work closely with cross-functional teams including marketing, medical affairs, creative, and design to ensure alignment of communication. You will participate in brand meetings and campaign discussions to align messaging with brand objectives and manage timelines and content delivery schedules across multiple brands/projects. Scientific storytelling and message framing will be a key component of your responsibilities, where you will translate complex scientific data into easy-to-understand messaging tailored for different audiences such as HCPs, field force, and patients. You will develop core claims, taglines, and campaign messaging based on product USPs and evidence base. Quality control and final checks will also be part of your duties, where you will conduct thorough QC of all assets for scientific accuracy, grammatical correctness, visual alignment, and brand consistency. To succeed in this role, you should have the ability to communicate scientific or medical information clearly and concisely, possess extensive knowledge of English grammar, and be familiar with a standard style guide. Previous experience in medico marketing and development of in-clinic, omnichannel, and CME collaterals is required. Proficiency in Word, Excel, PowerPoint, email, and the internet is essential, along with familiarity with basic principles of clinical research and the ability to interpret and present complex clinical data. The basic qualifications required for this position include a Bachelor's degree in biotechnology, BPharma, or life sciences with 2-3 years of medico-marketing writing experience, or a Master's degree in public health (MPH), M Pharma, BDS/MDS, or related fields with a minimum of 1 year of relevant experience.,