38 Scientific Knowledge Jobs

As a Content Editor & Proofreader at Biocon Biologics, your role will be crucial in ensuring error-free content produced by GMC. Your responsibilities will include: - Reviewing and proofreading global marketing content to maintain consistency in scientific language, terminology, grammar, style, and tone. - Checking for alignment with approved label, medical references, and brand messaging. - Ensuring compliance with regulatory and legal requirements for pharmaceutical communications across key markets (US, EU, etc.). - Assisting in developing high-quality training materials supporting global branding efforts. - Supporting launch and lifecycle marketing initiatives across therapy areas such a...

As a Senior Medical Writer, you will be responsible for developing content for pharmaceutical and healthcare marketing and communications materials. Your expertise is crucial in creating promotional materials, video scripts, objection handlers, and more to align with the strategic objectives of the brands you work on. You will collaborate closely with various teams to ensure a thorough understanding of each project and deliver accurate and engaging content to the target audience. **Key Responsibilities:** - Participate in planning and project meetings with internal and client teams as required. - Plan, develop, and write materials in alignment with strategic objectives. - Learn product and d...

• Communicate and collaborate with subordinates on goals. • Ensure complete strategy/system implementations as per directives • Induct new employee as per companys policy, ensuring no deviation while practicing policies and code of conduct • Guide team members to resolve issues, dealing with stockist & chemist. • Prepare and submit the tour programme for self and team as per the guidelines • Monthly analysis of Primary/ Secondary sales, customer coverage etc • Build business relationships with key customers • Brief sub-ordinates on the incentive scheme • Ensure Annual target Achievement of all HQ • Ensure achievement of all New Launches If Interested and have relevant experience, requesting ...

• Communicate and collaborate with subordinates on goals. • Ensure complete strategy/system implementations as per directives • Induct new employee as per companys policy, ensuring no deviation while practicing policies and code of conduct • Guide team members to resolve issues, dealing with stockist & chemist. • Prepare and submit the tour programme for self and team as per the guidelines • Monthly analysis of Primary/ Secondary sales, customer coverage etc • Build business relationships with key customers • Brief sub-ordinates on the incentive scheme • Ensure Annual target Achievement of all HQ • Ensure achievement of all New Launches If Interested and have relevant experience, requesting ...

• Communicate and collaborate with subordinates on goals. • Ensure complete strategy/system implementations as per directives • Induct new employee as per companys policy, ensuring no deviation while practicing policies and code of conduct • Guide team members to resolve issues, dealing with stockist & chemist. • Prepare and submit the tour programme for self and team as per the guidelines • Monthly analysis of Primary/ Secondary sales, customer coverage etc • Build business relationships with key customers • Brief sub-ordinates on the incentive scheme • Ensure Annual target Achievement of all HQ • Ensure achievement of all New Launches If Interested and have relevant experience, requesting ...

As a technology-led healthcare solutions provider, you will be part of a purpose-driven organization focused on enabling healthcare organizations to be future-ready. Indegene offers accelerated global growth opportunities for individuals who are bold, industrious, and nimble. You will experience a unique career journey at the exciting intersection of healthcare and technology, driven by passion, innovation, collaboration, and empathy. Key Responsibilities: - Develop, review, and edit scientific and medical content to meet International Quality Standards and client organization guidelines across various capabilities - Create content for regulatory, safety, medical affairs, medico-marketing, t...

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 handling complex Medical Writing projects, providing review support for medical writing deliverables, training junior writers, and authoring a broad set of different clinical document types that support regulatory filings. Your role will also involve leading cross-functional teams, understanding the clinical development process, and possessing effective communication, time management, organizational, and interpersonal skills. Key Responsibilities: - Prepare and review clinical study reports, protocols, investigator brochures, submission documents, and other regulatory documents on investigational drugs in various stages of clinical development. - Ap...

Description The Scientific Team Lead, India , operates as a core member of the global Syneos Health medical communications business. This leader will have line management and content delivery responsibilities for a team of 3-5 local medical writers of varying levels of seniority and experience. They will require the ability to effectively partner with local leadership and other key stakeholders in the organisation's global medical communications ecosystem. For the group's medical communication agency, Cadent, the Scientific Team Lead, India is a discipline subject-matter expert, who will join the existing medical writing footprint in India to manage a highly effective medical writing team, d...

• Communicate and collaborate with subordinates on goals. • Ensure complete strategy/system implementations as per directives • Induct new employee as per companys policy, ensuring no deviation while practicing policies and code of conduct • Guide team members to resolve issues, dealing with stockist & chemist. • Prepare and submit the tour programme for self and team as per the guidelines • Monthly analysis of Primary/ Secondary sales, customer coverage etc • Build business relationships with key customers • Brief sub-ordinates on the incentive scheme • Ensure Annual target Achievement of all HQ • Ensure achievement of all New Launches If Interested and have relevant experience, requesting ...

• Communicate and collaborate with subordinates on goals. • Ensure complete strategy/system implementations as per directives • Induct new employee as per companys policy, ensuring no deviation while practicing policies and code of conduct • Guide team members to resolve issues, dealing with stockist & chemist. • Prepare and submit the tour programme for self and team as per the guidelines • Monthly analysis of Primary/ Secondary sales, customer coverage etc • Build business relationships with key customers • Brief sub-ordinates on the incentive scheme • Ensure Annual target Achievement of all HQ • Ensure achievement of all New Launches If Interested and have relevant experience, requesting ...

• Communicate and collaborate with subordinates on goals. • Ensure complete strategy/system implementations as per directives • Induct new employee as per companys policy, ensuring no deviation while practicing policies and code of conduct • Guide team members to resolve issues, dealing with stockist & chemist. • Prepare and submit the tour programme for self and team as per the guidelines • Monthly analysis of Primary/ Secondary sales, customer coverage etc • Build business relationships with key customers • Brief sub-ordinates on the incentive scheme • Ensure Annual target Achievement of all HQ • Ensure achievement of all New Launches If Interested and have relevant experience, requesting ...

• Communicate and collaborate with subordinates on goals. • Ensure complete strategy/system implementations as per directives • Induct new employee as per companys policy, ensuring no deviation while practicing policies and code of conduct • Guide team members to resolve issues, dealing with stockist & chemist. • Prepare and submit the tour programme for self and team as per the guidelines • Monthly analysis of Primary/ Secondary sales, customer coverage etc • Build business relationships with key customers • Brief sub-ordinates on the incentive scheme • Ensure Annual target Achievement of all HQ • Ensure achievement of all New Launches If Interested and have relevant experience, requesting ...

As a Lead Medical Writer, you will be responsible for developing and reviewing medical writing deliverables that support the clinical regulatory writing portfolio. Your role will also involve training junior writers. You must have 4 to 6 years of experience in writing Clinical & Regulatory documents supporting global filings, specifically with experience in CTD Module 2 and Module 5. Your responsibilities will include preparing/reviewing clinical study reports, protocols, investigator brochures, submission data summaries, and other regulatory documents on investigational drugs at various stages of clinical development. You will apply lean authoring principles and coordinate activities for do...

As a Scientific Sales Executive, your primary responsibility will be to promote the company's products to doctors across various specialties. You will need to establish a strong understanding of all the products being promoted and effectively communicate this information during your interactions with customers. It is important to utilize your selling skills to generate demand and ensure that your actions align with the company's mission, vision, and values. You will be required to work closely with the scientific sales manager to execute the agreed-upon plan and provide regular feedback. Conducting Continuing Medical Education (CME) sessions and group meetings as per the agreed schedule will...

The Department of Chemistry and the Centre of Excellence in Mass Spectrometry (CoEMS) are currently looking for a Senior Technical Specialist to take on the lead technician role within CoEMS. In this position, you will be responsible for overseeing all key aspects of your specialist skills in mass spectrometry, as well as engaging in significant project collaborations and providing support to our academic group leaders in the Department of Chemistry. The Department of Chemistry at the University of York is globally recognized for its research and is committed to fostering an inclusive working environment where both staff and students are encouraged to excel. Holding an Athena SWAN Gold Award...

As a Drug Regulatory Affairs Manager at Covalent, you will be responsible for leading the Global Regulatory Project Team, comprising internal team members and external partners, to ensure the planning, preparation, and delivery of both simple and complex regulatory submissions and response documents on a global and regional scale. This includes maintaining core labeling documents, corporate approval of EU SmPC and US PI, and ensuring consistency with internal standards and SOPs. Your role will involve liaising with internal functions and external partners, leading cross-functional delivery teams, identifying regulatory risks, supporting routine and non-routine interactions with health author...

As a Technical And Scientific Expert (TSE) at Datwyler, you will play a crucial role in the high visibility and high impact area of healthcare. Your primary responsibility will involve collaborating with global pharmaceutical and biotech companies to develop innovative and life-saving drug packaging solutions. Working as a part of the Technical and Scientific Services (TSS) Team within Datwyler Healthcare, you will be based in the US and report directly to the Global Head of TSS. This team, which is customer-focused and operates on a global scale, collaborates closely with Sales, Marketing, and Product Management to achieve the business objectives of Datwyler Healthcare. Your role will entai...

As a Community Associate at Inito, you will play a crucial role in nurturing a supportive and engaging community for our users. Your responsibilities will involve welcoming new members, encouraging interactions, creating engaging content, and moderating discussions on platforms like Facebook and Reddit. By fostering a safe and lively space, you will help our community members feel informed, supported, and connected as they navigate their health journey. Collaborating with the community team, you will brainstorm and implement campaigns and interactive experiences to enhance community engagement. Your role will also include actively listening to members, addressing queries, showing empathy, mo...

You are a technology-led healthcare solutions provider, driven by the purpose to enable healthcare organizations to be future-ready. You offer accelerated global growth opportunities for individuals who are bold, industrious, and nimble. At Indegene, you can experience a unique career journey celebrating entrepreneurship, guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, visit www.careers.indegene.com. Imagine moving to an exciting role in an entrepreneurial organization without the usual risks associated with it. At this stage of your career where growth and variety are important to you, Indegene inv...

The role involves serving as the single point of scientific, administrative, and regulatory control for the study. You will actively participate and supervise all study activities, including animal dosing, clinical signs observation, data collection, and analysis, ensuring compliance with relevant regulations, OECD Principles of GLP, and SOPs. Additionally, you will be responsible for the operation, maintenance, and proper utilization of various equipment/instruments like centrifuges, laminar air flow systems, anesthetic machines, and syringe pumps. Your duties will also include the preparation and updating of SOPs relevant to in vivo and in vitro experiments. Moreover, you will be expected ...

We are a technology-led healthcare solutions provider driven by the purpose to enable healthcare organizations to be future-ready. We offer accelerated global growth opportunities for talent that is bold, industrious, and nimble. At Indegene, you will gain a unique career experience that celebrates entrepreneurship and is guided by passion, innovation, collaboration, and empathy. If you are looking to explore exciting opportunities at the convergence of healthcare and technology, visit www.careers.indegene.com. Jump-start your career with Indegene where we understand the importance of the first few years in shaping your professional journey. We promise you a differentiated career experience ...

Alkem Laboratories Limited is an Indian multinational pharmaceutical company headquartered in Mumbai, that manufactures and sells pharmaceutical generics, formulations and nutraceuticals in India and globally over 50 countries. The company has been consistently ranked amongst the top five pharmaceutical companies in India, with a portfolio that includes renowned brands like Clavam, Pan, Pan-D, and Taxim-O, which are among the top 50 pharmaceutical brands in the country. As a Medical Advisor at Alkem Laboratories Limited, your primary role will be to actively contribute to the organization by ensuring the scientific, technical, and ethical soundness of all policies, statements, and endeavors....

As a Medical Writer at Novartis Healthcare Private Limited, you will be responsible for writing, reviewing, and managing the production of high-quality clinical and safety documentation for submission to regulatory authorities in support of marketing applications. Your role will also involve providing authoritative documentation-related consultancy to other line functions and coaching, mentoring, and training less experienced writers. In this position, you will author, review, and independently manage complex Clinical Study Reports (CSR), Risk Management Plans (RMP), and other documents for health authorities. You will lead writing teams for complex submissions, contribute to key messaging a...

Communicate and collaborate with subordinates on goals. Ensure complete strategy/system implementations as per directives Induct new employee as per companys policy, ensuring no deviation while practicing policies and code of conduct Guide team members to resolve issues, dealing with stockist & chemist. Prepare and submit the tour programme for self and team as per the guidelines Monthly analysis of Primary/ Secondary sales, customer coverage etc Build business relationships with key customers Brief sub-ordinates on the incentive scheme Ensure Annual target Achievement of all HQ Ensure achievement of all New Launches