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Clinical Research Specialist

2 months ago

Beverly Hills, United States Cedars-Sinai Full time

Job Description

Are you looking to contribute to groundbreaking research? We look forward to having you join our team to collaborate on groundbreaking research

The Clinical Research Specialist provides clinical research expertise by participating in the design and implementation of research projects and care of research patients as needed. Responsible for specific and assigned aspects of research infrastructure development, coordinates projects, and communicates status and improvement areas to leadership. May implement and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Coordinates research projects at an institutional or departmental level. Serves as an internal consultant forspecific departmental activities. Communicates project status and improvement areas with leadership in a timely manner. Projects mayinclude, but are not limited to investigator-initiated protocol development including protocol writing, casereport form development, budget development, and coordination of departmental research committees. Provides mentorship regarding project planning, project logistics, and project implementation Participates in required training and education programs. Participates in weekly research staff meetings. Provides clinical expertise and support with quality assurance, performance improvement, and health plancompliance for clinical trial compliance. Ensures the completion and maintenance of consent forms, case report forms, SAE’s and source documentsto ensure that research is being conducted according FDA, HSPC, HIPAA an d other agency guidelines Completes appropriate IRB paperwork and submission/filing of internal and external SAEs to IRB.Responsible for insuring timely submission of complete, accurate and neat documents to research sponsors,IRB, and contract research organizations, where applicable. Acts as a liaison with Principal Investigators, pharmaceutical company representatives and other projectfunding organizations to supervise and update project progress. Prepares for institutional, pharmaceutical and internal audits, including facilitating third party studymonitoring. Attends site feasibility visits and site initiation visits for potential studies, and assures that new studies areimplemented according to protocol Review pertinent medical records to determine opportunities for quality improvement. Analyze qualitymetric data in support of the Principal Investigator and Director of Clinical Services. Recommend andimplement process improvement efforts. Assists with procedures, and supports related patient care when required during data collection process.

Qualifications

Educational Requirements:

Bachelor's Degree in related field preferred.

Master's Degree Preferred.

Licenses:

Basic Life Support (BLS) Certificationneeds to be the AHA HealthcareProvider Type Only, required/

SoCRA or ACRP or comparable certification

Experience:

5 years of experience in clinical research required.

5 years experience in IRB clinical research application procedures. Related experience in Pharmaceutical/Biotechnology, or Contract ResearchOrganization (CRO), preferred.

5years experience in Phase I, II, III, IV clinical trials and investigator initiatedtrials, preferred

Physical Demands:

Lifting, standing, walking, sitting

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

With a growing number of primary urgent and specialty care locations across Southern California, Cedars-Sinai’s medical network serves people near where they live. Delivering coordinated, compassionate healthcare you can join our network of clinicians and physicians to improve the healthcare people throughout Los Angeles and beyond.

Req ID

: HRC1413767 Working Title

: Clinical Research Specialist Department

: Research - CSMN Business Entity

: Cedars-Sinai Medical Care Foundation Job Category

: Academic / Research Job Specialty

: Research Studies/ Clin Trial Overtime Status

: EXEMPT Primary Shift

: Day Shift Duration

: 8 hour Base Pay

: $40.13 - $62.20 #J-18808-Ljbffr