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  • ID
    #52635058
  • Salary
    TBD
  • Source
    Dignity Health
  • Date
    2024-10-04
  • Deadline
    2024-12-02
 
Full-time

OverviewHello humankindness (https://hellohumankindness.org/)St. Joseph's Hospital and Medical Center is a 576 bed non-profit facility providing quality health care to patients and communities in and around Phoenix, Arizona. We are part of CommonSpirit Health which operates 139 hospitals and more than 1,000 care sites across 21 states, making our services accessible to nearly 1 in 4 U.S. residents.For the health of our community we are proud to be a tobacco-free campus.ResponsibilitiesYou will have the opportunity to play a critical role in ensuring that the Ivy Brain Tumor Center is able to deliver on its mission to identify new, lifesaving therapies for brain cancer patients. Your position will have the operational responsibilities as outlined below. It is expected that you will serve as a role model to the Ivy staff by demonstrating professionalism, maturity, effective communication skills, and sound judgment.

Serve as a clinical investigator role model by participating in clinical research.

Provide medical input into clinical development plans, study designs, and data analysis.

Facilitate innovative design, execution, and interpretation of clinical trials.

Build strong relationships with a network of principal investigators, external scientific specialists, and key opinion leaders.

Provide medical oversight to ensure the safety of study participants, including review of Adverse Events of Special Interest, Serious Adverse Events, and review of safety narrative reports.

Provide medical oversight for clinical trial medical activities outsourced to third party vendors.

Provide expert medical input for the preparation of regulatory documents and interactions with regulatory authorities.

Provide expert medical and scientific analysis and interpretation of data from ongoing studies and in literature.

Participate in the preparation of publications and presentations at scientific meetings.

Ensure compliance with GCP, FDA regulations and other relevant guidelines.

Provide didactic training for physicians and trainees on effective performance as site investigators and principal investigators.

Provide oversight of clinical research organization (CRO) activities.

Collaborate with the Director to generate interim progress reports for industry partnerships.

Provide oversight of trial data management, including review of patient-specific data collection.

Enhance the culture of patient safety, data integrity, and quality assurance within the clinical operations team.

QualificationsMinimum Education:

Medical Doctor or DO

Pay Range$80.00 - $750.25 /hourWe are an equal opportunity/affirmative action employer.

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