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Clinical Research Study Administrator

City of Hope
Posted 8 months ago, valid for 11 days
Location

Duarte, CA 91010, US

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • Join City of Hope as a Study Administrator and contribute to innovative research in the fight against cancer and other life-threatening illnesses.
  • The position requires at least three years of experience in clinical research, medical research, or public health, with a Bachelor's Degree or relevant certification.
  • Key responsibilities include managing research staff, overseeing data collection, and ensuring regulatory compliance.
  • Candidates with a Master’s Degree and prior experience in leading teams in a research setting are preferred.
  • Salary is based on work experience, qualifications, and work location, with a commitment to equal opportunity employment.

Join the forefront of groundbreaking research at City of Hope where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research.

A Study Administrator position is currently available.

As a successful candidate, you will:

  • Manage a team of research staff for multi-center research study and/or multiple research studies. 

  • Compilate, register and submit study data. Monitor project databases and maintain a system of effective data flow associated with research protocol(s).

  • Facilitate and manage multi-faceted data collection projects, which include preparation and quality control of the data as well as result tabulation.

  • Takes a lead role in preparing for IRB review of protocol(s) or maintaining continuing IRB approval of protocol(s), as well as assisting study staff to maintain regulatory compliance.

  • Oversee DPS Clinical Research Assistants (CRAs) and/or Phlebotomists’ specimen and data collection activities. 

  • Maintain a system for effective study management and tracking of data and specimen collection.

  • Serve as a resource for CRAs and/or Phlebotomists, and as a liaison between faculty, staff and other sites.

  • Serve as a technical resource for the assigned project and assists in training new staff members.

  • Be able to function independently and proficiently as defined in the position accountabilities.



Your qualifications should include:

  • Bachelor’s Degree or Certified CRA or Certified Tumor Registrar in lieu of degree.

  • Experience may substitute for minimum education requirements.

  • At least three years’ experience working in clinical research, medical research, or public health, or related field.

  • Experience managing multiple tasks.

Preferred education, experience and skills:

  • Master’s Degree.

  • Prior experience leading or supervising team members is strongly preferred, especially in a research or clinical setting.

 

City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.

City of Hope is an equal opportunity employer.

To learn more about our Comprehensive Benefits, pleaseCLICK HERE.




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