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Form of workWho 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 3,000 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.
What the Medical Director/Nurse Practioner Department Does at Worldwide
The Medical Director and Nurse Practioner department is responsible for providing the highest quality of care for all subjects enrolled in clinical studies. This department ensures all study participants are safe, meets with study participants, and reviews all study protocols for compliance.
What the Principal Investigator/Medical Director, Early Phase does at Worldwide
Ensures adherence to protocol requirements, protects the rights and welfare of subjects, and 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
- Possess a thorough understanding of the requirements of each protocol
- Assess the subject's response to therapy and evaluate for adverse experiences
- Secure written IRB approval before initiating the study or instituting any changes to the protocol as approved
- Document deviations from the approved protocol
- Assume responsibility for the investigational product at the trial site
What you will bring to the role
- At least 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.
- At least 2 years' experience in clinical research as an investigator or sub-investigator.
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.
Interested in hearing more about Worldwide or our roles? Check out our careers page at www.worldwide.com/careers!
