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Director, Regulatory and Medical Writing - Remote

Posted 10 weeks ago
All others
Full Time
USA

Overview

MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating.

Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.

MMS recognizes that a talented staff is what drives our business forward. Identifying and attracting top talent and continual training to strengthen core skills are essential to its core mission. At MMS, enthusiasm, collaboration, and teamwork are fostered, knowing that a global and diverse talent pool makes the company stronger. For more information, visit www.mmsholdings.com or follow MMS on LinkedIn.

We are looking for a motivated leader to join our Regulatory and Medical Writing Team!

In Short

  • Oversees a team of Regulatory and Medical Writers.
  • Accountable for performance, team engagement, coaching, and mentorship.
  • Proficient with QC, MW tools, training, and processes.
  • Works on complex issues requiring in-depth knowledge of the company.
  • Manages client meetings and CRMs.
  • Identifies and mitigates project risks.
  • Provides strategic input in Resource Management.
  • Functions as a Business Lead, promoting the service line.

Requirements

  • College graduate in Scientific, Medical, or Clinical discipline.
  • Minimum of 10 years’ experience in Regulatory or Medical Writing.
  • Prior direct line management experience required.
  • Ability to resolve potential problems with client demands.
  • Demonstrates managerial skill and experience.
  • Proficiency with MS Office applications.
  • Hands-on experience with clinical trial and pharmaceutical development preferred.
  • Good communication skills and willingness to work with others.
  • Excellent problem-solving skills.
  • Understanding of CROs and scientific and clinical data/terminology.

Benefits

  • High customer satisfaction rating.
  • Global footprint across four continents.
  • Focus on team collaboration and enthusiasm.
  • Opportunities for continual training and skill strengthening.

MMS

MMS

MMS is an award-winning, data-focused clinical research organization (CRO) that supports the pharmaceutical, biotech, and medical device industries. Recognized as a Great Place to Work certified organization, MMS boasts an exceptional culture and industry-leading employee retention rate. With a global presence across four continents, the company excels in providing scientific solutions to complex trial data and regulatory submission challenges. MMS is committed to fostering a collaborative and inclusive work environment, ensuring that employees can thrive while contributing to the future of clinical research.

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