medical-writer

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.  
 
We bring together a talented team of professionals with a deep understanding of patient and physician behaviors and market dynamics. 

Together we share insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients. 
 
Syneos Health supports a diverse, equitable and inclusive culture that cares for colleagues, customers, patients, communities and the environment.

Syneos Health

• Support accurate and compliant document filing within Veeva RIM
• Perform eTMF filing activities while adhering to GxP guidelines
• Manage document handling activities within Veeva
• Ensure documents meet quality and integrity standards
• Categorize documents systematically for retrieval

Medical Writer I – Project Specialist

Medical Writer I role focusing on document management within Veeva systems for clinical projects. Supporting compliance and adherence to GxP guidelines while collaborating with stakeholders.

• Conducts data integrity reviews of assigned documents to ensure accuracy and consistency across text, tables, and figures
• Cross-checks scientific content against cited references
• Verifies correct interpretation of scientific data from referenced sources
• Ensures all statements are appropriately source annotated
• Participates in internal and client-facing meetings
• Monitors timelines and budgets for assigned projects
• Serves as a member of the medical writing team for projects
• Provides feedback to the lead medical writer
• Copyedits assigned documents
• Manages assigned projects according to medical writing standard operating procedures

Medical Writer I, Quality Check

Medical Writer I ensuring data integrity and quality checks for clinical documents in a biopharmaceutical company. Collaborating with medical writing teams and participating in stakeholder meetings.

We are uniting science, technology and talent to get ahead of disease together.
Our community guidelines: https://gsk.to/socialmedia

• Completes assignments independently or for more complex documents, under guidance of a mentor
• Authors a range of clinical documents, including regulatory documents following defined templates
• Ensures high integrity of data interpretation, following negotiation with document team.
• Ensures the consistency and quality level of all documents that are issued.
• Actively participates in all planning, coordination and review meetings.
• Ability to work on 2-3 assignments simultaneously.
• Proactively raises and discusses concerns/ issues in an open and timely manner and within the global team.

Senior Medical Writer

Senior Medical Writer authoring and coordinating clinical documents for a biopharma company. Ensuring data integrity and quality of diverse regulatory submissions.

• Mentors and leads less experienced medical writers on complex projects
• Acts as lead for assigned writing projects
• Manages medical writing activities associated with individual studies
• Develops or supports a variety of documents
• Identifies and proposes solutions to resolve issues arising during the writing process
• Serves as peer reviewer on internal review team
• Performs on-line clinical literature searches as applicable
• Maintains familiarity with current industry practices and regulatory requirements

Senior Medical Writer – Abstracts, Manuscripts

Senior Medical Writer leading complex writing projects and managing writing activities at Syneos Health. Collaborating with medical teams while adhering to regulatory standards.

CorroHealth is a leading provider of clinically led healthcare analytics and technology-driven solutions, focused on enhancing the financial performance of hospitals and health systems. Their integrated solutions and advanced technologies aim to optimize the entire revenue cycle, offering services such as revenue cycle management, clinical documentation, medical coding, and denials management. With a commitment to improving financial health through intelligent technology and expert guidance, CorroHealth addresses complex payer-provider relationships and supports efficient healthcare operations.

CorroHealth is the leading provider of clinically led healthcare analytics and technology-driven solutions, dedicated to positively impacting the financial performance for physicians, hospitals, and health plans. With over 11,000 employees worldwide, CorroHealth offers integrated solutions, proven expertise, intelligent technology, and scalability to address needs across the entire revenue cycle. Our global presence extends over 10 locations, including the United States, India, and the United Kingdom, enhancing our ability to deliver exceptional service on a large scale.

CorroHealth

• Perform all or most of the primary duties listed below.
• Specific tasks and responsibilities may be outlined by the Leadership Team Member.

Senior Executive – Clinical Documentation Review

Sr Executive in Clinical Documentation helping clients with financial health goals in a hybrid work setup. Performing essential duties and responsibilities as per team objectives.

Allucent is a leading partner for small and mid-sized biotech companies, offering innovative regulatory and clinical development solutions. With over 30 years of experience, Allucent specializes in therapeutic expertise, clinical pharmacology, regulatory strategy, drug safety, and the pharmacovigilance processes needed to bring new therapies to market. Their comprehensive services address challenges from early-phase drug discovery through clinical trials and post-marketing surveillance, supporting various therapeutic areas such as oncology, infectious disease, neurology, autoimmune diseases, and rare diseases. Allucent's commitment to fostering breakthrough science helps biotech companies navigate the complexities of drug development efficiently and effectively.

Allucent is on a mission to help bring new therapies to light by solving the distinct challenges of small and mid-sized biotech companies. The company is purpose-built through the convergence of leading providers to address this unmet need. Today, Allucent is a global provider of comprehensive drug development solutions, including consulting, clinical operations, biometrics and clinical pharmacology across a variety of therapeutic areas. With more than 30 years of experience in over 60 countries, Allucent’s individualized partnership approach provides experience-driven insights and expertise to assist its clients in successfully navigating the complexities of delivering novel treatments to patients.

Allucent

• Assists with writing, editing and compiling written deliverables in the disciplines of chemistry, manufacturing, and controls (CMC), nonclinical, clinical, medical and regulatory for submission to regulatory agencies (e.g., U.S. Food and Drug Administration), sponsor use, or for publication or presentation 
• Contributes to scientific discussions regarding the planning, production and review of written deliverables 
• Develops knowledge of applicable regulatory agency requirements and guidance, applicable International Council on Harmonization (ICH) Guidelines, and other industry best practices 
• Develops knowledge of company templates, requirements, and resources related to the production of written deliverables 
• Assists in the development of templates and guidelines for regulatory and other written deliverables 
• Performs literature searches as applicable

Senior Medical Writer assisting in writing and compiling regulatory submissions in a hybrid environment at Allucent in Chennai, India.

• Collaborate with passionate problem solvers in biopharmaceutical solutions
• Accelerate the delivery of therapies while simplifying work processes
• Lead writing projects and manage related activities
• Compile and edit medical writing deliverables
• Maintain familiarity with current industry practices and regulatory requirements
• Perform on-line clinical literature searches, as applicable

Senior Medical Writer at Syneos Health translating insights into outcomes in medical writing. Collaborating to simplify work while leading medical writing projects within the biopharmaceutical industry.

Hybrid Medical Writers roles in India

Browse 7 hybrid medical writers roles hiring in India plus related opportunities such as medical reviewer and medical director.

7 jobs found

Medical Writer I – Project Specialist

Syneos Health

Medical Writer I, Quality Check

Syneos Health

Senior Medical Writer

GSK

Senior Medical Writer – Abstracts, Manuscripts

Syneos Health

Senior Executive – Clinical Documentation Review

CorroHealth

Senior Medical Writer

Allucent

Senior Medical Writer

Syneos Health