Medical Director - Investigator - San Antonio, TX - Office Based Join to apply for the Medical Director - Investigator - San Antonio, TX - Office Based role at Worldwide Clinical Trials
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Who We Are
Read on to find out what you will need to succeed in this position, including skills, qualifications, and experience.
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.
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.
Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law . Seniority level Seniority levelMid-Senior level
Employment type Employment typeFull-time
Job function Job functionHealth Care Provider
IndustriesResearch Services
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