Worldwide Clinical Trials | Medical Director

1 week ago

san antonio, United States Worldwide Clinical Trials Full time

Who we are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.


We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.


Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.


Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us


What the Medical Director-Investigator does at Worldwide

  • Ensures adherence to protocol requirements, protects the rights and welfare of subjects, assures the integrity of data generated at the site. The role directs the conduct of the clinical investigation according to federal and state regulations including guidance documents. Directly supervises all full-time, part-time, and PRN Investigators and Sub-Investigators. Indirectly supervises and oversees all clinical staff


What you will do

  • Ensure protocol compliance
  • Supports review by a duly constituted IRB
  • Manage the medical care of subjects
  • Protect the rights and welfare of subjects
  • Ensure the validity of the data reported to sponsors
  • Ensure documentation of study-related procedures, processes, and events
  • Ensure the proper use and storage of investigational agents
  • Support site operations


What you will bring to the role

  • Minimum of 2 years’ experience in performing physicals, assessing, and treating patients.
  • Strong supervision, interpersonal and communication skills.
  • Must possess exceptional organizational and planning skills and good documentation skills.
  • Must have good conflict resolution skills and be committed to quality.
  • Must be punctual and have a flexible work schedule to include on call, weekends and holidays if needed
  • At least 2 years’ experience in clinical research as an investigator or sub-Investigator.
  • In-depth knowledge of the clinical research process, including Good Clinical Practices.


Your experience

  • Required: Medical (M.D.) degree with at least 2 years of clinical research experience.
  • Preferred: Medical degree plus at least 5 years of clinical research experience with 2 years in Phase 1 research.



We love knowing that someone is going to have a better life because of the work we do.


To view our other roles, check out our careers page at Discover a world of difference at Worldwide For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

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