Senior Medical Writer

Lever, Inc.; India; Remote; INR 1,800,000 - 3,000,000; Full time

Benefits offered by this job

Remote work in Bengaluru, India

Global project exposure

Mentoring and knowledge sharing

Competitive compensation

Job summary

Lever, Inc. in Bengaluru, India, is seeking a Senior Medical Writer with deep expertise in clinical trial disclosure and transparency. The role will lead complex submissions across multiple jurisdictions, including protocol registrations, results postings, and anonymization packages.

You will provide strategic regulatory guidance to clients and internal teams, mentor junior colleagues, and drive process improvements to raise quality standards in disclosure workflows.

Qualifications

• Demonstrated professional experience in medical writing with specialization in clinical trial disclosure and transparency.
• Thorough knowledge of global clinical trial disclosure requirements and platforms.
• Extensive experience with protocol registration, results reporting, registry maintenance, and disclosure compliance strategies.
• Strong understanding of health literacy principles for patient-facing disclosures.
• Knowledge of data protection and anonymization techniques.
• Ability to mentor colleagues and lead complex disclosures across jurisdictions.

Responsibilities

• Lead preparation, review, and delivery of disclosure submissions across multiple jurisdictions.
• Develop and review protocol registrations, results postings, PLS, LPS, redaction and anonymization packages, and CCI tables.
• Apply medical writing expertise to CSRs, IBs, ICFs, clinical overviews, and safety reports.
• Provide regulatory guidance to clients and internal teams on disclosure requirements.
• Manage client interactions and complex disclosure projects from initiation to delivery.
• Interpret regulations and provide practical strategic recommendations.
• Ensure submissions comply with global regulatory requirements.
• Contribute to process improvements and best-practice development.
• Mentor junior team members on disclosure requirements and quality standards.

Skills

Medical writing

Clinical trial disclosure

Regulatory guidance

Stakeholder management

Data protection & anonymization

Planned/regulated documentation

Clear scientific communication

Education

Bachelor’s degree in life sciences

Tools

ClinicalTrials.gov

EudraCT

EU-CTR/CTIS

EMA Policy 0070

Health Canada requirements

Job description

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Medical Writer based in India.

This is a strategic opportunity for an experienced medical writer specializing in clinical trial disclosure and transparency.
You will lead complex disclosure projects from initiation through delivery, helping global clients meet evolving regulatory requirements.
The role combines advanced medical writing, regulatory interpretation, clinical document review, and client consulting.
You will work across submissions such as protocol registrations, results postings, plain language summaries, anonymization packages, and CCI justification documentation.
Your expertise will directly support transparency, data protection, and patient access to meaningful clinical trial information.
You will also contribute to process improvements while mentoring junior colleagues and raising quality standards across the team.
The position is well suited to a detail-oriented professional who can navigate complex regulations while communicating clearly with both technical and non-technical stakeholders.

Accountabilities:

• Independently lead the preparation, review, and delivery of clinical trial transparency and disclosure submissions across multiple jurisdictions.

• Develop and review protocol registrations, results postings, plain language summaries (PLS), lay protocol synopses (LPS), redaction and anonymization packages, anonymization reports, and CCI justification tables.

• Apply advanced medical writing expertise to clinical and regulatory documents, including study protocols, Clinical Study Reports (CSRs), Investigator Brochures (IBs), Informed Consent Forms (ICFs), clinical overviews, clinical summaries, and safety reports.

• Provide strategic and regulatory guidance to clients and internal teams on clinical trial disclosure and transparency requirements.

• Lead client interactions and provide consultation on complex disclosure and regulatory matters.

• Manage complex disclosure projects independently from initiation through final delivery, ensuring timelines, quality expectations, and regulatory requirements are met.

• Interpret applicable regulations and provide practical, strategic recommendations that support informed client decision-making.

• Ensure submissions and disclosure materials comply with applicable requirements across multiple global jurisdictions.

• Contribute to process improvement initiatives, best-practice development, and the continuous enhancement of disclosure workflows.

• Mentor and train junior team members on disclosure requirements, document preparation, regulatory compliance, and quality standards.

Requirements:

• Demonstrated professional experience in medical writing, with significant specialized expertise in clinical trial disclosure and transparency.

• Thorough knowledge of global clinical trial disclosure requirements and platforms, including ClinicalTrials.gov, EudraCT, EU-CTR/CTIS, EMA Policy 0070, and Health Canada requirements.

• Extensive experience with protocol registration, results reporting, registry maintenance, and clinical trial disclosure compliance strategies.

• Strong understanding of health literacy principles and proven ability to develop clear, accessible, patient-facing disclosure documents.

• Thorough knowledge of data protection requirements and their practical application to anonymization and redaction activities.

• Advanced expertise in identifying, assessing, and justifying personally identifiable data (PPD) and confidential commercial information (CCI) redactions.

• Strong understanding of clinical and regulatory documentation, with advanced writing and review capabilities.

• Excellent written and verbal English communication skills, with the ability to explain complex scientific and regulatory concepts clearly.

• Strong client-facing and stakeholder management skills, including the ability to provide confident regulatory guidance.

• Excellent attention to detail, organization, and ability to manage multiple complex projects independently.

• Bachelor’s degree in life sciences, health sciences, or a related field, or equivalent professional experience.

• Ability to mentor colleagues and contribute proactively to team knowledge, process improvement, and best-practice development.

Benefits:

• Full-time remote position based in Bengaluru, India.

• Opportunity to work on global clinical research and clinical trial transparency projects.

• Exposure to complex regulatory requirements across multiple international jurisdictions.

• Opportunity to collaborate with global clients and multidisciplinary clinical research teams.

• Professional development through mentoring, regulatory expertise, and involvement in process improvement initiatives.

• Meaningful opportunity to contribute to greater clinical research transparency and patient access to trial information.

• Opportunity to work within a global clinical research environment focused on advancing healthcare and life-changing therapies.