P

ProPharma Group

Regulatory sciences consultant for life sciences

Medical Information Writer

Technical WritingConfirmed live in the last 24 hours
Full-timeIndiaNo salary listed

About the Job

Requirements

  • A PharmD degree is required.
  • Excellent written communication skills are required.
  • Computer literacy is required.
  • Sound planning, prioritising and organisational skills are required.
  • Accuracy and attention to detail are required.
  • The ability to work within a team in an open and professional manner is required.

Responsibilities

  • Carry out comprehensive and accurate literature searches in Medline or other required databases for technical medical information letters or documents.
  • Prepare medical information letters and other documents using information gathered from literature searches or similar technical information, condensing technical data into concise and readable standard documents as needed.
  • Update existing written documents by checking that their information remains accurate and up to date, and incorporate new information from literature searches in appropriate places while maintaining readability and technical flow.
  • Ensure written items are accurate, readable, technically proficient, and compliant with ProPharma standard operating procedures and client-specific working practices.
  • Quality-check own work and, under guidance, check simple documents produced by others to ensure standards are met and maintained.
  • Maintain awareness of and comply with legal requirements and professional guidelines for providing medical information in the pharmaceutical and healthcare industries.
  • Adhere to the employment contract's confidentiality statement concerning ProPharma and client data and property.
  • Manage confidential information and personal data related to ProPharma and its clients in accordance with data privacy regulations and ProPharma standard operating procedures.
  • Work professionally with clients, customers, team members, and management.
  • Perform other duties as assigned.

About the Company

ProPharma Group

Regulatory sciences consultant for life sciences

ProPharma Group provides regulatory sciences consulting and related services for drugs, biologics, medical devices, and diagnostics on a global scale. Its offerings cover the full lifecycle, from early development and clinical trials to regulatory approval and post-market activities. The company’s services include regulatory sciences, clinical research, quality and compliance, pharmacovigilance, medical information, and R&D technology, delivered by a team of over 2,500 professionals with more than 20 years of operation. ProPharma Group differentiates itself by providing expert, end-to-end regulatory and life sciences solutions across multiple product types and stages, helping pharmaceutical, biotechnology, and medical device companies navigate complex regulatory and compliance challenges. The goal is to help clients bring safe and compliant products to market efficiently while maintaining ongoing lifecycle support.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Raleigh, NC
Founded
2001

Recently Posted Jobs

Explore more opportunities at ProPharma Group

See more jobs