14 Scientific Expertise Jobs

As an Associate Scientific Editor at STM Journals, you will be utilizing your PhD and author experience to support researchers in scholarly publication. Your role within the Author Heroes team involves collaborating with researchers to facilitate the publication of impactful scientific discoveries, focusing on rigorous peer review, ethics, and reproducibility. With a portfolio of 2700+ hybrid and open ACCESS scientific journals, you will actively contribute to advancing science, improving health outcomes, and fostering equitable participation in publishing. **Role Overview:** In this role, you will evaluate content as a partner to external editors, improve the editorial process for editors a...

As a Medical Affairs Specialist, you will play a pivotal role in supporting the marketing and sales teams with scientific expertise. You will collaborate across functions to ensure the accuracy and scientific integrity of marketing materials, product launches, and ongoing brand management. This role requires a deep understanding of scientific data and the ability to communicate it effectively to non-scientific stakeholders. - Conduct comprehensive literature reviews to support the creation of medical manuals, presentations, and marketing materials. - Lead the development of product launch presentations, delivering insights on therapy areas and product specifics to the marketing and sales tea...

As the Scientific Communications MLR Technical Reviewer at the company, your role involves checking all medical content for data and scientific accuracy, and reference appropriateness for materials submitted through the Medical, Legal, and Regulatory (MLR) process. It is your responsibility to ensure that all content aligns with Amgen's scientific and compliance standards, facilitating timely review and approval of assets that educate and engage healthcare providers, patients, and internal stakeholders. Working in collaboration with the US Scientific Communications MLR Reviewer, your scientific expertise, attention to detail, and compliance awareness play a crucial role in evaluating submiss...

As a Clinical Development Trial Lead (CDTL) at Lilly, you will play a crucial role in leading study teams of internal and external partners to plan and execute studies within the clinical plan. Your primary responsibility will be to ensure the quality, on-time, and on-budget fulfillment of study deliverables. Additionally, you may support non-study project assignments aimed at transforming and improving the business. You will be expected to seek knowledge from internal and external sources to shape development plans and identify continuous improvement opportunities. **Key Responsibilities:** - **Project Management and Regional Operational Knowledge:** - Understand the scope of work required ...

Role Overview: As the Evidence Generation Director at Novartis, you will play a crucial role in contributing to the product medical strategy and leading integrated evidence planning. Your expertise in evidence generation will empower cross-functional teams to excel in developing and executing integrated evidence strategies. You will need to possess strong scientific and technical knowledge in evidence generation across clinical trials and real-world settings, along with a deep understanding of product strategies, business dynamics, and healthcare environments. Success in this role hinges on your strategic thinking, leadership, collaboration, communication skills, and entrepreneurial mindset ...

As a Medical Science Liaison (MSL) in the field of oncology, your role will involve establishing and maintaining peer-level relationships with Key Opinion Leaders (KOLs) in both academic and private institutions. Your responsibilities will include delivering impactful, compliant, and timely scientific interactions aligned with the medical strategy. You will serve as the therapeutic guide for products spanning across various cancer indications such as renal, lung, breast, prostate, and ovarian. Additionally, you will provide clinical and scientific expertise to cross-functional teams and support regional medical education programs. Key Responsibilities: - Establish and maintain relationships ...

As a Toxicology and Ingredient Data Maintenance Analyst at Colgate-Palmolive, you will play a crucial role in maintaining the accuracy and integrity of product ingredient data to ensure compliance with global regulations. Your responsibilities will include managing and updating ingredient databases, collaborating with Research & Development and Supply Chain teams, conducting risk assessments, and providing toxicological support for product development and innovation. Additionally, you will be expected to respond to internal and external inquiries regarding product safety and ingredient information, ensuring data accuracy and consistency across various products and platforms. Adapting to the ...

The Clinical Reporting Unit at Novo Nordisk is seeking a skilled and experienced individual to join their team. As a Medical Writer, you will be responsible for performing high-complexity medical writing tasks and acting as a project manager. Your role will involve planning, developing, and overseeing various regulatory documents, including Protocols, Clinical Trial Reports, Investigator Brochures, and Regulatory response documents. Additionally, you will lead discussions, drive project strategy, and ensure clear communication of clinical data. In this position, you will also be expected to contribute to process improvements, knowledge sharing, and mentorship of other medical writers. Mainta...

We are looking for talented Scientific writers with a strong drive for results and enthusiasm for content creation, publication process, and healthcare to join our dynamic team. If you have a knack for breaking down complex medical concepts and transforming them into clear, concise content, we would love to have you on board. Key Details: Experience: 3-5 years of experience in medical writing with a proven record of delivering high-quality, accurate content. Salary: Competitive salary with attractive incentives for each assignment. Positions Available: 3 (on-site, Dr. D.Y.Patil Medical College, Hospital & Research Centre) Roles & Responsibilities: Utilise your scientific knowledge to profici...

Would you like to leverage your PhD and author experience to assist researchers in their scholarly publication journey About our Team At STM Journals, we collaborate closely with researchers to facilitate the publication of their impactful scientific discoveries. We prioritize rigorous peer review, ethics, and reproducibility. By supporting our extensive portfolio of 2700+ hybrid and open ACCESS scientific journals, you will actively contribute to advancing science, enhancing health outcomes, and promoting equitable participation in publishing. About the Role The Associate Scientific Editor position is part of the Author Heroes team. Team members utilize their scientific expertise and proble...

As a member of our team in the Diagnostic/Healthcare/Clinical Research industry, you will be responsible for leading and supporting the Research & Development efforts in clinical biochemistry. Your role will involve validating and optimizing biochemical assays and laboratory protocols, working closely with the laboratory, Quality Assurance, and medical teams. It will be essential to ensure compliance with NABL and other regulatory standards, while also providing scientific expertise to drive innovation and improvement in diagnostic services. This is a full-time position with benefits including Provident Fund. The schedule for this role is during day shifts, and the work location is in person...

As a member of our team in the Diagnostic/Healthcare/Clinical Research industry, you will be responsible for leading and supporting the Research and Development activities in clinical biochemistry. Your role will involve validating and optimizing biochemical assays and laboratory protocols, working closely with the laboratory, Quality Assurance, and medical teams. It will be your responsibility to ensure compliance with NABL and other regulatory standards while providing scientific expertise to drive innovation and improvement in diagnostic services. This is a full-time position with benefits including Provident Fund. The work schedule is during day shifts and the job location is in person. ...

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 the Lead Specialist GOE CAL at dsm-firmenich in Mumbai, you play a crucial role in bridging the gap between taste, texture, and health through innovative ingredients and solutions. Diversity, Equity & Inclusion is at the core of our values, ensuring equal access to opportunities, a sense of belonging, and authenticity celebrated across the organization. Your responsibilities include planning and conducting analytical techniques such as GC-MS, LC-MS for flavors, perfumes, and natural products, contributing to method development and the team's technical growth. You will manage analytical instruments, lab operations, ensure SOP compliance, accurate documentation, and collaborate closely with...