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Principal Med Writer

U73100MH2004PTC144454 PPD Pharmaceutical Development India Private Limited

LocationIndia
SeniorityPrincipal
CompanyU73100MH2004PTC144454 PPD Pharmaceutical Development India Private Limited
Verified recentlyChecked today
Compensation

Salary not listed

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Requirements and working style

Decision details from the source listing

Education

Master degree

Schedule

fixed

These fields are normalized from the employer's text. Confirm details on the employer site before applying.

WFH.team analysis

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.

Role lane

Data, Healthcare admin, Operations, Product, Sales, Security, Software, Writing and content

Where you can work

India

Working hours

Timezone overlap is not stated.

Arrangement

Principal · contract · full_time

Required signals
Medical writingClinical study reportsClinical study protocolsClinical and scientific document writing and reviewRegulatory documents (IBs, INDs, and MAAs)Regulatory requirementsQuality processesTherapeutic area expertise
Preferred signals
Program managementDocument development softwareProcess improvementProject timelines and budgetsClient presentations and proposal review
Confirm before applying
  • Required timezone overlap is not stated
  • Compensation is not listed
Market context

Data hiring on WFH.team

11,338active related roles
4,042new in the latest period
405.5jobs per 100 candidates
$165kmedian of comparable listed ranges

Category counts come from WFH.team's latest published remote job market snapshot.

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Skills and signals
Medical writingClinical study reportsClinical study protocolsClinical and scientific document writing and reviewRegulatory documents (IBs, INDs, and MAAs)Regulatory requirementsQuality processesTherapeutic area expertiseProgram managementDocument development softwareProcess improvementProject timelines and budgetsClient presentations and proposal reviewFully remote in India; listing also references a Mumbai office location.
Job description

Principal 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.