Regulatory Documentation Specialist CLIN BIOSCIENCES

1.0 - 5.0 years

0 - 0 Lacs

bangalore, chennai, hyderabad

On-site

Roles and Responsibilities Prepare, edit, format, and manage regulatory documents including: Clinical study protocols & reports Investigator brochures Common Technical Documents Modules 25 Risk Management Plans Briefing documents and response packages. Work closely with regulatory affairs, clinical, safety, medical writing, and quality assurance teams. Maintain version control and document tracking using electronic document management systems. Review, QC, and validate documents to ensure scientific accuracy and editorial consistency. Required Skills: Excellent written communication and technical documentation skills. Knowledge of regulatory submission processes and eCTD structure. Familiarit...

Posted 2 months ago

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Scientific Affairs Executive CLIN BIOSCIENCES

1.0 - 3.0 years

0 - 0 Lacs

bangalore, chennai, united arab emirates

On-site

Roles and Responsibilities; Provide scientific support for internal teams, marketing, and field medical teams Prepare scientific documents including slide decks, Q&A documents, clinical summaries, product dossiers, and white papers Review promotional and medical materials for scientific accuracy and compliance Stay up to date with the latest scientific literature and product-related publications Collaborate with Medical Affairs, Regulatory, and Pharmacovigilance departments Respond to medical information queries from field force and customers Ensure compliance with medical, ethical, and promotional guidelines Eligibility / Qualifications: B.Pharm / M.Pharm / M.Sc. in Life Sciences, Microbiol...

Posted 2 months ago

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Medical Communications Specialist CLIN BIOSCIENCES

1.0 - 6.0 years

0 - 0 Lacs

hyderabad, bangalore, united arab emirates

On-site

Roles and Responsibilities; Develop and review scientific content for clinical/scientific presentations, brochures, product monographs, patient education materials, slide decks, and white papers. Translate complex medical/scientific data into clear, engaging, and compliant communication for various audiences. Assist in the creation of publication plans, scientific abstracts, peer-reviewed articles, and regulatory documents. Collaborate with cross-functional teams including medical affairs, regulatory, pharmacovigilance, marketing, and clinical research. Ensure all content complies with company SOPs, regulatory standards, and industry codes. Conduct literature reviews, gap analysis, and conte...

Posted 3 months ago

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Medical Affairs Manager CLIN BIOSCIENCES

3.0 - 7.0 years

0 - 0 Lacs

bangalore, united arab emirates, hyderabad

On-site

Roles and Responsibilities; Provide scientific and clinical support to internal teams, field force, and external stakeholders. Develop and deliver medical education, scientific slide decks, advisory boards , and KOL engagement plans . Lead product monograph development , scientific publications , and medical content review . Collaborate with regulatory, R&D, pharmacovigilance, and marketing on product lifecycle. Participate in medical strategy development , ensure compliance with promotional practices. Ensure all materials meet global and local medical, ethical, and regulatory standards . Work with Medical Science Liaisons (MSLs) for field-based scientific engagement. Manage clinical studies...

Posted 3 months ago

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Medical Safety Physician Diensten Tech Limited

3.0 - 8.0 years

4 - 7 Lacs

Gurgaon / Gurugram, Haryana, India

On-site

Description We are seeking a highly motivated Medical Safety Physician with 3-8 years of experience to join our team. As a Medical Safety Physician, you will be responsible for ensuring patient safety and compliance with regulatory requirements. You will work closely with cross-functional teams to develop and implement safety strategies for our products. Responsibilities Develop and implement medical safety strategies for our products Manage safety-related issues and concerns from clinical trials through to post-marketing surveillance Ensure compliance with regulatory requirements and guidelines Provide medical expertise and guidance to cross-functional teams Conduct safety reviews of clinic...

Posted 4 months ago

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