Senior Medical Writer
2 days ago
Job Title: Senior Medical Writer Location: MS Clinical Research (MSCR),Department: Medical & Scientific AffairsReporting To: DirectorExperience Required: Minimum 10 years in medical/scientific writingEngagement Type: Consultant – Part-time/Project-based/RemoteRole Summary:MSCR is seeking a highly experienced Senior Medical Writer to oversee the medical writing function and mentor a growing team of in-house writers. This strategic role will involve managing complex writing projects, reviewing and enhancing document quality, and providing expert guidance to ensure scientific accuracy, regulatory compliance, and writing excellence across all deliverables.Key Responsibilities:Lead and manage medical writing assignments including protocols, clinical study reports, regulatory documents, manuscripts, abstracts, and presentations.Mentor and supervise junior and mid-level medical writers providing developmental feedback, training, and quality review.Ensure consistency, clarity, and scientific accuracy across all documents.Review and approve materials related to clinical trial registration (e.g., CTRI entries) and ethics committee submissions.Guide the team on best practices for literature review, referencing, and scientific integrity using sources like PubMed, NIH Library, and NLM databases.Provide strategic input on publication planning, conference material development, and stakeholder communications.Collaborate closely with cross-functional teams including researchers, project managers, and external consultants to align on deliverables.Maintain up-to-date knowledge of global regulatory writing standards (e.g., ICH-GCP, GPP3, CONSORT).Recommend and implement process improvements, templates, and SOPs for documentation.Provide oversight for version control, formatting, and adherence to SOP MSCR/GEN/03-03.Required Qualifications:PhD/MD/MPharm/MSc in Life Sciences, Medicine, or Pharmacy.Minimum 6 years of medical writing experience, preferably in a CRO or clinical/preclinical research setting.Demonstrated experience managing or mentoring a team of writers.Strong command of written English and scientific communication.Proficiency with referencing tools (e.g., EndNote) and document management systems.Excellent organizational and project management skills.Preferred Skills:Experience in preclinical (in-vitro/in-vivo) and clinical trial documentation.Exposure to publication strategy and submission to peer-reviewed journals.Familiarity with tools like CTD structure, CTRI submission portals, and regulatory publishing platforms.Benefits:Competitive salary and compensation package.Flexible working hours and remote work options.Opportunity to work with a dynamic and collaborative team.Professional development and growth opportunities.
-
Senior Medical Writer
7 hours ago
Bengaluru, India MS CLINICAL RESEARCH Full timeJob Title: Senior Medical Writer Location: MS Clinical Research (MSCR), Department: Medical & Scientific Affairs Reporting To: Director Experience Required: Minimum 10 years in medical/scientific writing Engagement Type: Consultant – Part-time/Project-based/Remote Role Summary: MSCR is seeking a highly experienced Senior Medical Writer to oversee the...
-
Senior Medical Writer
16 hours ago
Bengaluru, India MS CLINICAL RESEARCH Full timeJob Title: Senior Medical Writer Location: MS Clinical Research (MSCR),Department: Medical & Scientific AffairsReporting To: DirectorExperience Required: Minimum 10 years in medical/scientific writingEngagement Type: Consultant – Part-time/Project-based/RemoteRole Summary:MSCR is seeking a highly experienced Senior Medical Writer to...
-
Senior Medical Writer
16 hours ago
Bengaluru, India MS CLINICAL RESEARCH Full timeJob Title: Senior Medical WriterLocation: MS Clinical Research (MSCR),Department: Medical & Scientific AffairsReporting To: DirectorExperience Required: Minimum 10 years in medical/scientific writingEngagement Type: Consultant – Part-time/Project-based/RemoteRole Summary:MSCR is seeking a highly experienced Senior Medical Writer to oversee the medical...
-
Senior Medical Writer
16 hours ago
Bengaluru, India MS CLINICAL RESEARCH Full timeJob Title: Senior Medical WriterLocation: MS Clinical Research (MSCR),Department: Medical & Scientific AffairsReporting To: DirectorExperience Required: Minimum 10 years in medical/scientific writingEngagement Type: Consultant – Part-time/Project-based/RemoteRole Summary:MSCR is seeking a highly experienced Senior Medical Writer to oversee the...
-
Senior Medical Writer
53 minutes ago
Bengaluru, India Celegence Full timeJob Description Company Description Celegence provides services and solutions to support the Life Sciences industry with regulatory affairs operations and strategy, helping companies navigate global regulatory requirements. With expertise across all phases of the product lifecycle, including regulatory strategy, submission management, and health authority...
-
Senior Medical Writer
1 week ago
Bengaluru, India ICON Full timeSenior Medical Writer ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Senior Medical Writer to join our diverse and...
-
Senior Medical Writer
1 week ago
Bengaluru, Karnataka, India Ergomed Full time ₹ 20,00,000 - ₹ 25,00,000 per yearCompany Description Ergomed is a rapidly expanding full service mid-sized CRO specializing in Oncology and Rare Disease. Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia. Our company allows for employee visibility (you have...
-
senior medical writer
3 weeks ago
bengaluru, India Randstad Full timeMedical Communication Writer to lead content development across scientific, branded, and consumer-friendly formats. This role involves scientific communication, medical storytelling, and omnichannel asset creation for pharma, medical device, and healthcare. Responsibilities:· Draft, review, and edit high-quality content: research...
-
Medical Writer
3 weeks ago
Bengaluru, India Trigent Software - Professional Services Full timePosition: Senior Medical Writer – RWELocation: Bangalore Job Type: Full-time Department: Medical Writing – MCAPLJob DescriptionThe Senior Medical Writer – RWE will be responsible for authoring, reviewing, and managing high-quality scientific and regulatory documents. The role requires strong scientific understanding, writing expertise, and the ability...
-
Medical Writer
3 weeks ago
Bengaluru, India Trigent Software - Professional Services Full timePosition: Senior Medical Writer – RWELocation: BangaloreJob Type: Full-timeDepartment: Medical Writing – MCAPLJob DescriptionThe Senior Medical Writer – RWE will be responsible for authoring, reviewing, and managing high-quality scientific and regulatory documents. The role requires strong scientific understanding, writing expertise, and the ability to...
