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 content referencing from PubMed, Embase, Medline, etc. Attend medical conferences, KOL discussions, and advisory boards for content development and insight gathering. Qualifications & Experience: B.Pharm / M.Pharm / PharmD / MBBS / BDS / BAMS / MSc (Life Sciences, Biotechnology, Microbiology) Certification or diploma in medical writing or scientific communication (preferred) Interested to apply can share you CV in Whatsapp/Call to 9342735755

Posted 1 day 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 (IIS/phase IV) in coordination with clinical operations teams. Eligibility / Qualifications: MBBS / MD / PharmD / Ph.D. / M.Pharm (Pharmacology / Clinical Pharmacy / Life Sciences) Knowledge of therapeutic areas, ICMJE, ICH-GCP, GVP , and Indian regulatory guidelines Strong experience in scientific writing, medical review, and stakeholder interaction Interested to apply can share you CV in Whatsapp/Call to 9342735755

Posted 2 days 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 clinical trial protocols, study reports, and regulatory submissions Collaborate with internal and external stakeholders to assess and manage safety risks Participate in safety signal detection and assessment activities Contribute to the development and implementation of risk management plans Provide medical review of adverse event reports and ensure timely reporting to regulatory authorities Skills and Qualifications Medical degree (MBBS/MD) with 3-8 years of experience in medical safety or pharmacovigilance Knowledge of global regulatory requirements and guidelines related to drug safety Experience in safety surveillance and risk management activities Excellent analytical and problem-solving skills Ability to work independently and collaboratively in a cross-functional team environment Strong communication and interpersonal skills Attention to detail and ability to manage multiple tasks simultaneously Experience in conducting safety reviews of clinical trial protocols, study reports, and regulatory submissions

Posted 1 month ago

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