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\xe2\x80\x99re 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\xe2\x80\x99ll prepare clinical documents for comprehensive clinical trials and programs. Using compliant Parexel and sponsor formats, styles and management systems, you\xe2\x80\x99ll 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\xe2\x80\x99re 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\xc2\xb4s 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.

Medical Writer II - 4+ years of Experience. The Medical Writer II will research, create, edit, and coordinate the production of clinical documents associated with submissions to regulatory authorities, including but not limited to: study protocols, model informed consents, interim and final clinical study reports, and safety update reports. The Medical Writer II will also be responsible for the production of clinical study documentation associated with clinical trials that may not be included in a regulatory submission. The Medical Writer II may serve as the primary client contact. Bachelor\'s degree in Life Sciences/Health Related Sciences or equivalent.
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