Salary not listed
Salary details are shown when available from the source listing. Sign in before applying so the role can be reviewed against your resume, salary goals, seniority, timezone, and location eligibility.
Decision details from the source listing
Master degree
fixed
These fields are normalized from the employer's text. Confirm details on the employer site before applying.
What this posting tells you
Principal medical writer role leading and reviewing clinical and scientific documents, including study reports, protocols, IBs, INDs, and MAAs. Includes mentoring junior staff, advising on document strategy and regulatory practices, and potentially serving as backup program manager. Listed as fully remote in India, with a standard Monday–Friday schedule.
Data, Healthcare admin, Operations, Product, Sales, Security, Software, Writing and content
India
Timezone overlap is not stated.
Principal · contract · full_time
- Required timezone overlap is not stated
- Compensation is not listed
Data hiring on WFH.team
Category counts come from WFH.team's latest published remote job market snapshot.
Explore the remote job marketPrincipal Med Writer at U73100MH2004PTC144454 PPD Pharmaceutical Development India Private Limited
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. As the lead writer, reviews documents for the team and provides training and guidance to junior team members. Provides advice on document development strategy, regulations and industry best practices. Demonstrates subject matter and therapeutic area expertise. Acts as backup program manager. Collaborates with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.
Researches, writes, and edits clinical study reports and study protocols, and summarizes data from clinical studies.
Researches, writes, and edits clinical study reports and study protocols, and summarizes data from clinical studies.
- Serves as primary author who writes and provides input on complex clinical and scientific and program level documents, including IBs, INDs, and MAAs.
- Provides senior level review of routine and complex documents. Provides training and mentorship for other writers and program managers on document preparation, the use of software for document development, document types, regulatory requirements, and therapeutic area knowledge.
- Ensures compliance with quality processes and requirements for assigned documents. As the subject matter expert, develops and reviews best practices, methods and techniques for achieving optimal results, including various client-specific processes, and leads process improvement initiatives. May also develop, review and manage performance metrics for assigned projects.
- May serve as backup program manager. Identifies and resolves out-of-scope activities. Duties could include developing timelines, budgets, forecasts and contract modifications, and assisting business development with client presentations and proposal text review and attending bid defense meetings and capabilities presentations.
- Represents the department at project launch meetings, review meetings, and project team meetings.