Job Description

Parexel's Regulatory Medical Writing Services works closely with our clients around the world to develop and launch new medicines and treatments that improve healthcare for millions of patients. We’re one of the largest providers of medical writing services worldwide, and have managed thousands of writing projects in more than 29 countries across North and South America, Europe, Asia, and Africa. As a result of continued customer satisfaction and business growth, this global team is expanding and offers many opportunities for career development. In this role, you’ll prepare clinical documents for comprehensive clinical trials and programs. Using compliant Parexel and sponsor formats, styles and management systems, you’ll manage clinical document deliverables such as model informed consent forms, clinical study reports, pharmacovigilance documents and more. Our Medical Writers also participate in ongoing professional development programs to maintain current knowledge in the various areas. Explore opportunities within our core Clinical Development, Biotech, or Functional Service Provider (FSP) teams below.

• Full Time
• Travel: No
• Glassdoor Reviews and Company Rating

Success Profile

Check out the top traits we’re looking for and see if you have the right mix.

• Detail-Oriented
• Deadline-Oriented
• Communicator
• Organized
• Versatile
• Tech-Savvy

Rewards

• Global Impact

  We are one truly global team working together to propel each client´s journey ahead faster.

• Work-life Balance

  We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.

• Career Development

  Opportunity to learn and grow through a performance and development goal-setting program.

• Home based

  Love where you work, and work where you love.

• Variety

  Opportunity to work on a wide range of therapeutic areas, document types and clinical projects.

Senior Medical Writer 7 or more years of regulatory medical writing experience and hands-on experience in CSRs, protocols, IBs, and submission documents These roles will require a good understanding of complex regulatory writing processes including analytical skills, data interpretation & skills to communicate information to target audiences. The ideal candidate must possess a good understanding of clinical trials and drug development, have a sound knowledge of scientific methodology and statistical principles in the design, conduct and description of clinical research. Must demonstrate a robust understanding of how to interpret, describe and document clinical data and must have excellent English language skills (verbal and written).