3.0 - 7.0 years

0 Lacs

chennai, tamil nadu

On-site

Role Overview: As a Medical Writer at RRD GO Creative, you will be responsible for developing high-quality and scientifically accurate medical and regulatory documents, including clinical study reports, protocols, and brochures. Your role involves creating clear and concise medical content tailored for healthcare professionals, regulatory agencies, and internal stakeholders. Conducting thorough research and literature reviews to ensure content accuracy and compliance with industry standards is essential. Collaboration with subject matter experts, scientists, and regulatory teams is crucial to develop compelling and compliant medical writing materials. You will also need to adhere to client a...

Posted 1 month ago

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Global HEOR Systematic Literature Review Senior Associate Amgen

3.0 - 7.0 years

0 Lacs

hyderabad, telangana

On-site

Role Overview: As a Global Systematic Literature Review (SLR) Senior Associate in the Global Health Economics & Outcomes Research (HEOR) department at Amgen, your primary responsibility is to provide expertise in designing, executing, and managing literature review services. You will collaborate closely with the team lead and Global HEOR Product Leads to align with HEOR product strategy. Your role is crucial in supporting global access to Amgen's therapies by generating high-quality, evidence-based outputs across the product lifecycle. Key Responsibilities: - Refine literature review questions in alignment with the team lead and prepare research protocols. - Design literature searches for el...

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Lead Medical Writer Tatvacare

5.0 - 9.0 years

0 Lacs

ahmedabad, gujarat

On-site

As the Lead Medical Writer at Tatvacare, you will be responsible for developing and reviewing high-quality medical content, including scientific publications such as original research articles, consensus reports, review articles, and clinical trial documentation. Your role will involve collaborating with cross-functional teams, providing scientific expertise, and ensuring compliance with regulatory and industry standards. The ideal candidate for this position will have extensive experience in medical writing, particularly in clinical development, regulatory affairs, and digital health research. Your key responsibilities will include developing and finalizing medical writing documents, coordi...

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Consultant- Evidence Strategy Trinity Lifesciences

3.0 - 7.0 years

0 Lacs

haryana

On-site

You are a passionate and intellectually curious health economics and outcomes research (HEOR) research specialist looking to join Trinity's Evidence Strategy / HEOR team. In this role, you will provide strategic and tactical support to biotech, pharma, and medical device clients in evidence planning, value creation, and scientific communication through real-world HEOR. As a Consultant located in Gurgaon, India, you will be responsible for conducting systematic literature reviews using PRISMA guidelines, developing search strategies, screening and selecting studies, extracting and synthesizing data, and analyzing findings to draw evidence-based insights. Additionally, you will work on various...

Posted 3 months ago

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Medical Writer RRD GO Creative

3.0 - 7.0 years

0 Lacs

chennai, tamil nadu

On-site

RRD GO Creative is seeking experienced Medical Writers to join our team in Chennai. In this role, you will play a crucial part in developing high-quality and scientifically accurate medical and regulatory documents, such as clinical study reports, protocols, and brochures. Your responsibilities will also include creating clear and concise medical content tailored for healthcare professionals, regulatory agencies, and internal stakeholders. To excel in this role, you must conduct thorough research and literature reviews to ensure content accuracy and compliance with industry standards. Collaborating with subject matter experts, scientists, and regulatory teams is essential to develop compelli...

Posted 3 months ago

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