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Cedars-Sinai Clinical Research Coordinator II/CPT - Medically Associated Science & Technology Program (MAST) - Mathur Lab in Los Angeles, California

When the work you do every single day has a crucial impact on the lives of others, every effort, every detail, and every second matters.

This shared culture of happiness, passion, and dedication pulses through Cedars-Sinai, and it’s just one of the many reasons why we rank as one of the top hospitals in the nation by U.S. News & World Report. From working with a team of committed healthcare professionals to using state-of-the-art facilities, you’ll have everything necessary do something incredible—for yourself and for others.

Do you have a passion for helping human kind?

The MAST program at Cedars-Sinai Medical Center is dedicated to the development of novel drugs and devices to diagnose and treat patients. This innovative program is working to develop new diagnostics and therapeutics to treat patients with illnesses related to imbalances or alterations in the microbiome. Over the last 20 years, the MAST team has made many discoveries that benefit millions of patients, and we hope to help millions more with our growing fleet of novel diagnostics and therapeutics. To learn more, please visit: https://www.cedars-sinai.org/research/areas/science-tech.html

Our research is focused on associates between acute gastroenteritis and disruption of gut flora, impairment of GI tract motility, and small intestinal bacterial overgrowth in the pathophysiology of irritable bowel syndrome. There is a strong focus on clinical and translational research. Projects may include, but are not limited to invetigator-initiated protocol development including protocol writing, case report form development, budget development, and coordination of departmental research committees.

Additional Job Duties and Responsibilities:

  • Responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries.

  • Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; presents this information at regular research staff meetings.

  • May plan and coordinate strategies for increasing research participant enrollment, improving efficiency, training of personnel, or identifying new research opportunities.

  • Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB).

  • Communicates project status and improvement areas with leadership in a timely manner.

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Educational Requirements:

  • Bachelor of Arts or Sciences degree, required

Experience:

  • Four (4) years minimum of directly related experience required

License/Certification/Registration Requirements :

  • California Certified Phlebotomy Technician I or Certified Phlebotomy Technician II certification, or a valid California Nursing License

  • ACRP/SoCRA (or equivalent) certification preferred

Cedars-Sinai is an EEO employer. Cedars-Sinai does not unlawfully discriminate on the basis of the race, religion, color, national origin, citizenship, ancestry, physical or mental disability, legally protected medical condition (cancer-related or genetic characteristics or any genetic information), marital status, sex, gender, sexual orientation, gender identity, gender expression, pregnancy, age (40 or older), military and/or veteran status or any other basis protected by federal or state law.

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