Job Description
Job Description: • Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager • Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy • Compile and maintain project-specific status reports within the clinical trial management system • Interact with the internal project team, Sponsor, study sites, and third-party vendors • Provide oversight and quality control of our internal regulatory filing system • Provide oversight and management of study supplies • Create and maintain project timelines • Coordinate project meetings and produce quality minutes Requirements: • PhD in Life Sciences area is required; upcoming PhD graduates or Postdocs are welcome to apply! • A background in one of our key therapeutic focus areas: Cardiovascular, Renal / Nephrology, GI/Gastrointestinal/Gastroenterology • Fluency in English with solid presentation skills • Ability to work in a fast-paced dynamic industry Benefits: • Flexible work environment • Competitive PTO packages, starting at 20+ days • Competitive compensation and benefits package • Company-sponsored employee appreciation events • Employee health and wellness initiatives • Community involvement with local nonprofit organizations • Discounts on local sports games, fitness gyms and attractions • Modern, ecofriendly campus with an on-site fitness center • Structured career paths with opportunities for professional growth • Discounted tuition for UC online programs • Awards Named a Top Workplace in 2024 by The Cincinnati Enquirer • Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility Apply tot his job
Ready to Apply?
Don't miss out on this amazing opportunity!
🚀
Apply Now