Roivant Sciences

👥 501-1000💰 $230,000,000 Post-IPO Equity about 2 years ago🫂 Last layoff about 2 years agoPharmaceuticalBiotechnologyBiopharmaProduct ResearchHealth Care📈 Public Company
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Roivant Sciences is a biopharmaceutical company accelerating the development of promising late-stage drug candidates. We achieve this by building and supporting nimble, entrepreneurial biotech companies (Vants), leveraging a unique approach to talent acquisition, incentive alignment, and technology deployment. Our focus is on reducing the time and cost of bringing new medicines to market, ultimately improving patient lives and benefiting the healthcare system. We've successfully launched VTAMA®, achieved multiple FDA approvals, and secured significant global partnerships. This rapid growth has been fueled by strategic in-licensing, acquisitions, and a commitment to innovation. Our tech-enabled approach is central to our success. We utilize a robust technology stack including iPhone/Mobile compatibility, Google Tag Manager, Google Analytics, and a Content Delivery Network (CDN), ensuring efficient data management and streamlined operations. We foster a dynamic, collaborative environment, embracing both remote and in-person work models. Our engineering culture values agility, innovation, and a data-driven approach to problem-solving. Roivant's mission is to dramatically improve healthcare outcomes. We are a large company, currently employing between 501 and 1000 people, and we strive to create a rewarding and impactful workplace. We value both individual achievement and collaborative teamwork. We offer a range of exciting opportunities across multiple therapeutic areas, in both clinical development and tech-focused operations. Our significant funding and consistent success position us for continued growth and leadership in the biopharmaceutical industry. Roivant prioritizes diversity, equity, and inclusion. We are proud of our diverse workforce and offer a supportive and inclusive environment where every employee's contributions are valued. We embrace remote work, offering flexibility and empowering employees to perform at their best, regardless of location. With offices globally, we're a dynamic organization continually seeking talented and passionate individuals to join our mission.

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📍 United States

🔍 Pharmaceutical

  • MD, DO, or non-US equivalent with residency in Internal Medicine or equivalent.
  • Minimum 5 years at the Medical Director or Senior Medical Director level in CRO or Pharma.
  • Experience in planning and conducting clinical trials.
  • Familiarity with cross-functional teams including pharmacovigilance and regulatory affairs.
  • Desirable: late phase clinical trial experience in autoimmune disorders; board certification in Rheumatology.
  • Provide clinical scientific leadership for the clinical study team.
  • Oversee medical safety and CRO medical monitors.
  • Collaborate in pharmacovigilance and clinical operations.
  • Lead the design and writing of clinical protocols and documents.
  • Prepare and present safety data to monitoring boards.
  • Contribute to manuscripts and publications.

LeadershipGCPCommunication SkillsCollaborationAttention to detailCross-functional collaboration

Posted 2 months ago
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🧭 Full-Time

🔍 Pharmaceutical

  • Bachelor's Degree in a scientific discipline; advanced degree preferred.
  • 15+ years of clinical operations management experience, including trial leadership experience.
  • Demonstrated ability to set and prioritize goals, with excellent time management and problem-solving skills.
  • Strong leadership skills with a track record of delivering on-time execution and results.
  • Proven excellence in managing multiple trials and vendors in dispersed project team environments.
  • Leadership responsibility for Clinical Operations strategy, initiation, and execution of clinical trials across all phases, including CRO/vendor selection.
  • Oversee all aspects of study progress, ensuring adherence to Good Clinical Practice and regulatory guidelines.
  • Serve as Clinical Operations point of contact for strategic governance bodies and support regulatory filings.
  • Identify and qualify CROs and vendors for clinical trials, establishing governance procedures for continuous performance oversight.
  • Implement technologies and tools to improve enrollment projections and support effective communication with stakeholders.
Posted 3 months ago
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