Clinical Research Assistant II

City of HopeDuarte, CA

About The Position

Join the forefront of groundbreaking research at the Beckman Research Institute of 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. The Research and Training Division is seeking a Clinical Research Assistant II to support supportive care, cancer and aging studies conducted by a multidisciplinary research team. You will work closely with Assistant Research Faculty to prepare, manage, and clean research data for analysis, with a strong preference for candidates who have experience with data management and basic statistical methods. Your responsibilities also include recruiting and consenting patients for supportive care and cancer and aging studies, coordinating study activities, and assisting with regulatory and study documentation. The ideal candidate is detail-oriented, comfortable working with clinical and research data, and able to collaborate effectively with investigators, clinicians, and research staff in a team-based environment. Experience in clinical research, patient-facing recruitment, and data/statistical work is strongly preferred.

Requirements

  • Associates degree. Experience may substitute for minimum education requirements.
  • 2 years of experience working in a health care setting, preferably in research.

Nice To Haves

  • Bachelors preferred.
  • Experience with medical record review, health information systems, and/or clinical trials is preferred

Responsibilities

  • Conduct protocol management of multiple research protocols.
  • Maintain current and accurate protocol documentation
  • Ensure participants are appropriately registered and maintain documentation of participant registration.
  • Compile and submit data on appropriate forms according to protocol requirements.
  • Ensure protocol compliance with intense monitoring of specific study requirements.
  • Play an active role in recruiting patients to study.
  • Help train and mentor new clinical research staff members.
  • Collect and deliver specimens for analysis
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