Medical Director, Phase I Clinical Research, Entry Level or Experienced

Requisition Number: 2380

Position Title: Medical Director - Investigator

External Description:

Summary: Do you love helping people and making a difference through research? Are you an M.D. with a focus in Family Medicine or Internal Medicine? Are you tired of dealing with insurance and just want to focus on the patient? Then apply today for our Medical Director opportunity located in San Antonio, TX

About Worldwide Clinical Trials, Early Phase: Located in San Antonio, TX Worldwide’s Clinical Pharmacology Unit (CPU) is a top-notch full-service phase 1 clinical research facility focused on providing superior customer service to our subjects, sponsors, and developing our internal team members to grow their careers. Founded by physicians we are focused on offering a #uncommon experience to our employees and our customers.

About You: You will be a forward-thinking, people-focused individual with a passion for helping people and making a difference in the research industry. To be a great fit for this opportunity, you will have your Medical Doctor degree and an active license in the state of Texas. You will really stand out if you have experience in Clinical Research, Family Medicine, or Internal Medicine, interfacing with upper-level management and sponsors. For more of the day-to-day responsibilities see below.

Responsibilities:

Tasks may include but are not limited to:

• Possesses a thorough understanding of the requirements of each clinical protocol. Determine whether inclusion/exclusion criteria apply to the study population,
• Maintains protocol compliance and does not implement any protocol deviations or changes without agreement by the sponsor and prior review and approval by the IRB (except to eliminate immediate hazards to the subject),
• Reviews the inclusion/exclusion criteria, schedules visits, endpoint criteria, and investigational article use with the research team.
• Provides the IRB with adequate information to review the study. Secures written IRB approval before initiating the study or instituting any changes to the protocol as approved,
• Ensures that a qualified physician is responsible for all trial-related medical decisions, assesses subject response to therapy, evaluates and addresses adverse experiences
• Meets regularly with the research team to discuss subject participation and protocol progress,
• Trains Sub-Investigators.
• Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

Skills & Abilities:

• At least 2 years experience in performing physicals, assessing, and treating patients.
• Strong supervision, interpersonal and communication skills. 
• Must be punctual and have a flexible work schedule.    

Education Requirements:

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

 

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City:

State: Texas

Employment Type: Regular

Community / Marketing Title: Medical Director, Phase I Clinical Research, Entry Level or Experienced

Company Profile:

We’re a global, mid-size CRO that pushes boundaries, innovates and invents — because the path to a cure for the world’s most persist diseases is not paved by those who play it safe, but by those who take pioneering, creative approaches, and implement them with quality and excellence. We are experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs, in the best possible way.

Location_formattedLocationLong: San Antonio, Texas US

CountryEEOText_Description: 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 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. Worldwide is committed to working with and providing reasonable accommodations to applicants with disabilities. We are proud to be an equal opportunity workplace where people thrive by being themselves and are inspired to do their best work every day.