PHARMAFull-time
Senior Medical Writer
By Admin · Medical & Scientific Writing
BANGALORE (IN)REMOTEPOSTED: 10/7/2026
PHARMAFull-time
HIRING ORGANIZATIONPAREXELBiosciences / Healthcare, Contract Research Organization (CRO)
ROLE OVERVIEW
Parexel is hiring a Senior Medical Writer for its India-Bengaluru-Remote team. The role focuses on clinical trial disclosure and transparency, with responsibilities spanning regulatory document writing, disclosure submissions, client guidance, project management, and mentoring.
ROLE DEFINITION & RESPONSIBILITIES
- •Independently prepare and review clinical trial transparency submissions
- •develop protocol registrations and results postings
- •prepare plain language summaries and lay protocol synopses
- •manage anonymization, redaction, and CCI justification documentation
- •author and review clinical and regulatory documents
- •advise clients and internal teams on disclosure requirements
- •manage complex disclosure projects through delivery
- •mentor junior team members and support disclosure process improvements
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- Medical writing experience with expertise in clinical trial disclosure and transparency
- thorough knowledge of global clinical trial disclosure and transparency regulations
- experience with protocol registration, results reporting, registry maintenance, and disclosure compliance strategies
- bachelor's degree in life sciences, health sciences, or related field or equivalent professional experience
REQUIRED VERIFIED SKILLS
Clinical trial disclosure and transparency
ClinicalTrials.gov
EudraCT
EU-CTR/CTIS
EMA Policy 0070
Health Canada requirements
protocol registration
results reporting
registry maintenance
health literacy
data protection
anonymization
redaction
Personally Identifiable Data (PPD)
Confidential Commercial Information (CCI)
regulatory document authoring
client communication
mentoring
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
ORGANIZATION CONTEXT & CULTURE
Parexel is a global clinical research organization serving biopharmaceutical companies, medical device manufacturers, and academic institutions through clinical research and clinical development services.
TEAM SIZE: 20,000+ employees
INDUSTRY: Biosciences / Healthcare, Contract Research Organization (CRO)
APPLICATION ADVISORY
Highlight experience in clinical trial disclosure and transparency, particularly protocol registration, results reporting, registry maintenance, and disclosure compliance. Emphasize familiarity with ClinicalTrials.gov, EudraCT, EU-CTR/CTIS, EMA Policy 0070, Health Canada requirements, anonymization, redaction, PPD, and CCI. Clinical and regulatory document authoring experience should also be clearly demonstrated.
RECOMMENDED TRAINING
1/2
READY TO SUBMIT?
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