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Heart Institute Clinical Research Assoc I/CPT, Dr. Cheng Lab
Heart Institute Clinical Research Assoc I/CPT, Dr. Cheng LabCedars-Sinai • Los Angeles, CA, United States
Heart Institute Clinical Research Assoc I / CPT, Dr. Cheng Lab

Heart Institute Clinical Research Assoc I / CPT, Dr. Cheng Lab

Cedars-Sinai • Los Angeles, CA, United States
26 days ago
Job type
  • Full-time
Job description

Job Description

The Smidt Heart Institute reflects Cedars-Sinai's steadfast commitment 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 specialized 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 an increasing array of minimally invasive procedures, Cedars-Sinai continues to stand at the forefront of technology, innovation and discovery improving patient outcomes.

Join our team and use your experience with an organization known nationally for excellence in research!

The Clinical Research Associate I / CPT works under the direction of a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising staff to assist in tasks supporting the coordination / implementation of noncomplex research studies. Supports objectives of research studies through noncomplex tasks such as data collection, prescreening of potential and scheduling of current research participants, assisting in IRB submission activities, budget and billing, and ensuring overall compliance with all federal and local guidelines.

Primary Duties and Responsibilities

Works under the direction of a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising staff to assist in tasks supporting the coordination / implementation of noncomplex research studies.

Collects, evaluates and / or abstracts clinical research data. May assist in designing forms for data collection / abstraction. Enters and processes clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.

Completes Case Report Forms (CRFs)

Assists with prescreening of potential research participants for various clinical trials. Schedules research participants for research visits and research procedures. Provides supervised patient contact or independent patient contact for long term follow-up patients only.

Assists supervising staff with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines

Assists with clinical trial budgets and patient research billing

Responsible for sample preparation and shipping and maintenance of study supplies and kits.

Ensures compliance with protocol and overall clinical research objectives. 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

May serve as one point of contact for external sponsors for select trials. May respond to sponsor inquiries and attend meetings regarding study activity under the direction of supervising staff.

Qualifications

Educational Requirements :

High school diploma / GED required

Bachelor's degree in Science, Sociology or related degree preferred

Licenses :

  • CPT- Phlebotomy Certification license required

Experience :

1 year clinical research experience preferred

Physical Demands :

Able to perform moderate lifting.

Able to sit, stand and walk for prolonged periods of time.

Able to read papers and online documents.

Able to operate standard office equipment.

Able to exercise physical ability and perspective acuity to satisfactorily perform essential job functions.

Req ID : 9809

Working Title : Heart Institute Clinical Research Assoc I / CPT, Dr. Cheng Lab

Department : Heart Institute

Business Entity : Cedars-Sinai Medical Center

Job Category : Academic / Research

Job Specialty : Research Studies / Clin Trial

Overtime Status : NONEXEMPT

Primary Shift : Day

Shift Duration : 8 hour

Base Pay : $19.50 - $32.86

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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Research Institute • Los Angeles, CA, United States

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