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Cedars-Sinai Clinical Research Associate I in Los Angeles, California

Job Description

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.

We invite you to consider this phenomenal opportunity!

As a Clinical Research Associate I, you will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the study. This role evaluates and abstracts research data, and ensures compliance with protocol and research objectives. Position is responsible for completing case report forms (CRFs), entering clinical research data, and assisting with regulatory submissions to the Institutional Review Board (IRB). The CRA I may have limited contact with research participants as needed for study and assists with study budget and research participant billing. This role follows all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care.

Primary Job Duties and Responsibilities:

  • Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.

  • Provides supervised patient contact or patient contact for long term follow-up patients only.

  • Works closely with supervising research staff or directly with the Institutional Review Board to submit Adverse Events, Serious Adverse Events, and Safety Letters following local and federal guidelines.

  • Assists with clinical trial budgets and patient research billing.

  • Schedules patients for research visits and research procedures.

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

  • 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 including CSMC phlebotomy-specific clinical oversight which encompasses initial training, monthly assessments, six-month assessments, and annual assessments.

  • Performs phlebotomy services according to CSMC policies and procedures.

  • Verifies specimen identification, assesses appropriateness of test orders and quality of specimen by recognizing factors that affect procedures and results; takes appropriate action when corrections are indicated

  • Identifies patients and patient specimens by strict adherence to established procedures; labels samples accurately and completely.

  • Reports test results to appropriate individuals and exercises professional discretion with patient information.

Department-Specific Responsibilities:

  • Works directly with principal investigator in various clinical research studies

  • Assist with study patient enrollment and consents

  • Assists with writing scientific abstracts and protocols.

Qualifications

Education:

  • High School Diploma/G.E.D., required.

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

Licenses/Certifications:

  • ACRP/SoCRA (or equivalent) certification is preferred.

Experience:

  • Clinical Research experience is highly preferred.

  • Understanding of general research objectives.

Physical Demands:

Standing, Walking, Sitting, Lifting 50 lbs., Carrying 50 lbs., Pushing 75 lbs., Pulling 75 lbs., Climbing (Rarely), Balancing (Rarely), Stooping (Rarely), Eye/Hand/Foot Coordination, Crouching (Rarely), Crawling (N/A), Reaching, Handling, Grasping, Feeling, Talking, Hearing, Repetitive Motions, Kneeling (Rarely)

About Us

Cedars-Sinai is a leader in providing high-quality healthcare encompassing primary care, specialized medicine and research. Since 1902, Cedars-Sinai has evolved to meet the needs of one of the most diverse regions in the nation, setting standards in quality and innovative patient care, research, teaching and community service. Today, Cedars- Sinai is known for its national leadership in transforming healthcare for the benefit of patients. Cedars-Sinai impacts the future of healthcare by developing new approaches to treatment and educating tomorrow's health professionals. Additionally, Cedars-Sinai demonstrates a commitment to the community through programs that improve the health of its most vulnerable residents.

About the Team

Cedars-Sinai is one of the largest nonprofit academic medical centers in the U.S., with 886 licensed beds, 2,100 physicians, 2,800 nurses and thousands of other healthcare professionals and staff. Choose this if you want to work in a fast-paced environment that offers the highest level of care to people in the Los Angeles that need our care the most.

Req ID : HRC1452834

Working Title : Clinical Research Associate I

Department : Research - Surgery Chair

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 - $29.87

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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