Scientific Writer Clinforge Clinical Research Solutions Pvt. Ltd.

13.0 - 17.0 years

0 Lacs

lucknow, all india

On-site

You will be responsible for the following key tasks: - Developing, writing, and editing scientific manuscripts, review articles, case studies, and conference abstracts/posters. - Preparing regulatory and clinical documents such as clinical study reports, investigator brochures, patient information leaflets, and regulatory dossiers. - Creating medical communication materials like slide decks, CME content, and white papers tailored for healthcare professionals. - Collaborating with researchers, clinicians, and regulatory teams to ensure accuracy, consistency, and compliance with journal/regulatory requirements. - Conducting literature reviews and ensuring referencing accuracy using platforms l...

Posted -1 days ago

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Scientific Writer Clinforge Clinical Research Solutions Pvt. Ltd.

13.0 - 17.0 years

0 Lacs

lucknow, uttar pradesh

On-site

You will be responsible for the following key tasks: - Develop, write, and edit various scientific manuscripts, review articles, case studies, and conference abstracts/posters. - Prepare regulatory and clinical documents such as clinical study reports, investigator brochures, patient information leaflets, and regulatory dossiers. - Create medical communication materials including slide decks, CME content, and white papers tailored for healthcare professionals. - Collaborate effectively with researchers, clinicians, and regulatory teams to ensure accuracy, consistency, and compliance with journal/regulatory requirements. - Conduct thorough literature reviews and ensure precise referencing usi...

Posted 2 months ago

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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...

Posted 3 months ago

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