Clinical Research Specialist I - Clinical Research Office (Onsite)

Clinical Research Specialist I - Clinical Research Office (Onsite) Employer Cedars-Sinai Location Beverly Hills, California Salary Competitive Closing date 28 May 2024 Discipline Health Science Job Type Researcher Employment - Hours Full time Duration Permanent Qualification PhD Sector Hospital You need to sign in or create an account to a job.
Job Description Grow your career at Cedars-Sinai! Cedars-Sinai offers a culture of happiness, passion, and dedication.
This is one of the many reasons why we rank as one of the top hospitals in California and in the nation by U.
S.
News & World Report.
The Clinical Research Specialist I provides clinical research expertise by participating in the design and implementation of research projects as needed.
The incumbent is responsible for specific and assigned aspects of research infrastructure development, coordinates projects, and communicates status and improvement areas to leadership.
The team member in this role may implement and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts, and ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB).
Primary Duties and Responsibilities: Coordinates research projects at an institutional or departmental level.
Communicates project status and improvement areas with leadership in a timely manner.
Projects may include, but are not limited to investigator-initiated protocol development including protocol writing, case report form development, budget development, and coordination of departmental research committees.
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.
Department-Specific Responsibilities: The Clinical Research Specialist is responsible for efficient management of the SOCCI Data Safety Monitoring Committee as well as other major projects that are needed to support the CCTO.
Provides project management support by coordinating meetings and materials primarily for the Data Safety Monitoring Committee (DSMC) meetings and secondarily to the Protocol Review and Monitoring Committee (PRMC).
Independently prioritizes workload and performs a comprehensive review of all cancer related clinical research study monitoring, audit and safety reports and responses to be reviewed by the DSMC, within the appropriate timelines, and implements the operations of the DSMC.
Incorporates knowledge of the principles of clinical trials conduct, in order to assess the readiness of research protocol reports and other review documents for review by the DSMC.
Identifies the need for any ad-hoc members and works with the Chair to assign reviewers.
Serves as the primary point of contact for DSMC inquiries and provides technical support for investigators and staff.
Maintains all DSMC required documentation and ensures accurate recording of DSMC reviews into the clinical trial management system (OnCore).
Attends all DSMC committee meetings, ensuring procedures are followed and that minutes of committee meetings are taken, reviewed, and stored in an organized manner.
Assists in implementing modifications to the committee charters, establishment of processes, training materials or committee documentation.
Finds opportunities to better meet the National Cancer Institute (NCI) criteria for feasibility and scientific review of protocols and ongoing data safety and protocol monitoring.
Ensures meeting materials (e.
g.
, SAE reports, protocol deviation reports, etc) are organized with the goal of enhancing review of information by the committee and aid in decision making.
Onboards and trains new DSMC members.
Works with CCTO management to establish and optimize metric reports.
Regularly evaluates DSMC process for areas of inefficiency, and works with CCTO management to propose and implement changes for improving processes, and upon approval incorporates changes into the SOP and Charter.
Co-authors committee decisions on responses to investigators, assures these are reviewed, signed by the DSMC Chair, and communicated promptly to the investigator.
Communicates in a timely manner with Leadership regarding significant or time sensitive issues that arise that my hinder processing of reviews.
Assists in management of SOCCI Protocol Review and Management Committee by serving as a backup when necessary.
Assist in the management of the day-to-day operations and system applications associated with Clinical Trial Reporting Program (CTRP), including registering required CCTO trials in CTRP and abstracting relevant information from protocol and CTMS for submission to the CTRP Registration Site.
Assists with quarterly reporting of minimum elements of patient accrual information (for Complete and Abbreviated trials) either via the CTRP Accrual Registration Web Site; or Accrual Batch file submission.
Works closely with PIs and study teams, and monitor CTMS data entries, to assure that all applicable trials are registered on the CTRP Registration as required by NCI policies.
Verifies and troubleshoots protocol web summaries (Trial Summary Report, TSR and xml file) as developed by CTRP, and maintain the CTRP electronic protocol listing.
This function requires understanding of CTRP reports in light of submitted trial information.
Performs other related duties as assigned or directed by Leadership to meet the goals and objectives of the CCTO.
Qualifications Education: Bachelor's degree (BA or BS) is required.
Licenses/Certifications: Certification through a professional organization such as Regulatory Affairs Professional Society (RAPS) or The Society of Clinical Research Associates (SOCRA) preferred.
Experience: 3 years of related experience in a similar position is required.
Prior monitoring or auditing experience in clinical research preferred.
Strong knowledge of federal, state, and local regulations regarding the conduct of clinical trials, the informed consent process, and protection of human subjects.
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.
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 : HRC1240635B Working Title : Clinical Research Specialist I - Clinical Research Office (Onsite) Department : Cancer - SOCCI Clinical Research Business Entity : Cedars-Sinai Medical Center Job Category : Academic / Research Job Specialty : Research Studies/ Clin Trial Overtime Status : EXEMPT Primary Shift : Day Shift Duration : 8 hour Base Pay : $32.
00 - $52.
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