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Research Support Assistant (Per Diem) - Heart Institute - Bairey-Merz Lab

Job Description - Research Support Assistant (Per Diem) - Heart Institute - Bairey-Merz Lab

Description

Grow your career at Cedars-Sinai!


The Smidt Heart Institute reflects Cedars-Sinai's steadfast dedication to heart disease and research innovation giving patients access to the highest level of care. Year after year, thousands of people trust their hearts to Smidt Heart Institute at Cedars-Sinai. Our cardiologists, cardiac surgeons and niche care teams treat the full spectrum of heart disease and disorders, while our investigators continue to advance the field with groundbreaking, life-saving research. From genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures, Cedars-Sinai continues to stand at the forefront of technology, innovation and discovery improving patient outcomes.


Are you ready to be a part of breakthrough research?


The Research Support Assistant provides clerical support to Clinical Research Associate, Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Research Manager. This role will provide the administrative support for research protocols by providing document management, obtaining proper signatures, and maintaining samples, kits, and study supplies. This role will comply with all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care.


Primary Duties and Responsibilities:



  • Completes data entry and manages documents for research activities and provides clerical support to the department.

  • Handles the process of obtaining the proper signatures for research grants and protocols.

  • Provides administrative support for research protocols.

  • Completes sample preparation and shipping and maintains study supplies and kits.

  • Responsible for obtaining outside research records for patients enrolled in protocols.

  • Schedules research meetings.

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

  • Maintains research practices using Good Clinical Practice (GCP) guidelines.

  • Maintains strict patient confidentiality according to HIPAA regulations and applicable law.

  • Participates in required training and education programs.



Qualifications

Education:



  • High School Diploma/GED is required.


Experience and Skills:



  • No experience is required. Previous coursework and experience in related field is preferred.



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