Senior Medical Writer
Location: Remote, India
Job ID: R-01332283
Employment Type: Full-Time
Category: Clinical Research
Work Mode: Fully Remote
Work Schedule: Standard (Monday to Friday)
About the Role
A leading global clinical research organization is seeking an experienced Senior Medical Writer to support high-impact clinical research and drug development programs. This role plays a critical part in delivering high-quality medical and scientific documents that support regulatory submissions, clinical studies, and strategic communications across multiple therapeutic areas.
As part of a globally recognized clinical research services team, the Senior Medical Writer will collaborate closely with internal and external stakeholders to ensure accurate, compliant, and timely delivery of clinical and regulatory documentation. The position offers the opportunity to contribute directly to advancing innovative therapies addressing complex global health challenges.
Key Responsibilities
Serve as the primary author for clinical and scientific documents, including clinical study reports, study protocols, and summaries of clinical data
Research, write, and edit complex regulatory and program-level documents such as Investigator’s Brochures (IBs), Investigational New Drug applications (INDs), and Marketing Authorization Applications (MAAs)
Manage the medical writing process from document planning and coordination through final delivery to internal and external clients
Demonstrate subject matter and therapeutic area expertise across assigned projects
Review and provide quality oversight for documents prepared by junior medical writers
Mentor and train junior team members and program managers on document preparation, regulatory standards, and medical writing best practices
Ensure full compliance with internal quality systems, client-specific processes, and global regulatory guidelines
Contribute to the development and continuous improvement of medical writing standards, methodologies, and best practices
Support program management activities, including scope management, timeline development, budget forecasting, and contract modifications when required
Represent the medical writing function in project launch meetings, review meetings, and cross-functional team discussions
Education and Experience Requirements
Bachelor’s degree in a scientific discipline or related field (advanced degree preferred)
Minimum of 5 or more years of professional medical writing experience, with demonstrated ability to independently author clinical and regulatory documents
Prior experience in the pharmaceutical, biotechnology, or Contract Research Organization (CRO) industry is strongly preferred
Formal certifications in medical writing or regulatory affairs (AMWA, EMWA, RAC) are advantageous
Equivalent combinations of education, training, and relevant experience may be considered
Required Skills and Competencies
Excellent medical and scientific writing skills, including data interpretation, grammar, editing, and proofreading
Strong understanding of global, regional, and national regulatory and document development guidelines
In-depth knowledge in at least one specialty area, such as clinical development, regulatory submissions, therapeutic areas, or scientific communications
Proven project management skills with the ability to manage multiple deliverables and deadlines
Strong interpersonal, problem-solving, and decision-making capabilities
Effective negotiation and stakeholder management skills
Exceptional written and verbal communication skills, including presentation abilities
Proficiency with document management systems and client templates
Strong computer skills, including Microsoft Word, Excel, Outlook, and related applications
Working Environment
Fully remote role based in India
Office-based work environment with virtual collaboration across global teams
Why This Opportunity
This role offers the chance to work within a high-performing global clinical research organization at the forefront of bringing new therapies to market. The Senior Medical Writer will play a vital role in supporting regulatory success, operational excellence, and scientific integrity across diverse clinical programs.
Equal Employment Opportunity
The organization is committed to providing equal employment opportunities to all qualified individuals without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other legally protected status.
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