Join our Medical Writing team and play a key role in delivering high-quality scientific and regulatory documents that support clinical development programmes worldwide. As a Medical Writer (Consultant), you will lead and contribute to a variety of medical writing projects, collaborating with cross-functional teams and clients to ensure the delivery of accurate, compliant, and impactful documentation. What You'll Do Medical Writing & Document Development - Author, review, and quality-check a range of regulatory and scientific documents, including clinical study reports and other medical writing deliverables. - Ensure all documents accurately reflect source data, meet regulatory requirements, and comply with company and client standards. - Manage document review cycles, resolve reviewer comments, and coordinate feedback from multiple stakeholders. - Provide editorial support, proofreading, and quality control reviews where required. - Project Leadership & Delivery - Manage multiple writing projects simultaneously, ensuring delivery within agreed timelines and budgets. - Track project milestones, risks, and progress using project management tools. - Collaborate closely with project teams, reviewers, and subject matter experts to ensure efficient project execution. - Maintain accurate project records, including time reporting and tracking metrics. Client Partnership & Business Support - Serve as a point of contact for clients on assigned projects. - Build and maintain strong client relationships through professional communication and high-quality delivery. - Mentoring & Knowledge Sharing - Provide training, guidance, and mentorship to junior Medical Writers and team members.



- Support process improvement initiatives and help drive innovation within the Medical Writing function. Regulatory & Industry Expertise - Stay current with evolving regulatory requirements, GCP standards, and scientific communication guidelines. - Share regulatory updates and industry best practices with colleagues and clients. - Engage with relevant industry forums and skilled networks to maintain expertise and awareness of emerging trends. Quanticate is the world leading data-focused CRO, and we often work with our customers on their complicated clinical trials which require a high level of statistical programming, statistics and data management input. We need talented individuals to help us fulfil our customers’ needs. Our customers range from top global pharmaceutical companies where you can work as an integrated team member on a world leading clinical program, to small biotechs that are taking their first steps in clinical development. We strongly advocate career development providing membership to professional societies, encouraging your involvement in their activities and committees. Together we can help you build the career you want – developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter. Requirements What You'll Bring Qualifications - Master's degree in Life Sciences, Medical Sciences, Pharmacy, or a related scientific discipline. - A PhD, PharmD, MD, MVSc, or equivalent advanced qualification is desirable. Experience - 4+ years of medical writing experience within the pharmaceutical, biotechnology, CRO, or healthcare sector. - Strong experience preparing regulatory and scientific documents.

📌 Clinical Trials Medical Writer (India)
🏢 Quanticate
📍 India