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Clinical Research Specialist II – Neurosurgery
Cedars-Sinai. Participate in the design and implementation of clinical research projects .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical research project design and implementation, ensuring compliance with GCP, FDA, and HIPAA regulations. Proficient in developing scientific documents and coordinating departmental research initiatives.
Highest-signal resume keywords
Clinical Research Project DesignGood Clinical Practice (GCP)FDA ComplianceHIPAA RegulationsProtocol Development
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Research Infrastructure DevelopmentProject CoordinationBudget DevelopmentCase Report Form DevelopmentScientific Document Development
Soft Skills
CommunicationProject PlanningGuidance
Industry Keywords
Institutional Review BoardClinical Trial RecruitmentResearch Quality ManagementPatient Confidentiality
About the role
Key responsibilities & impact- Participate in the design and implementation of clinical research projects
- Develop research infrastructure and coordinate assigned projects
- Coordinate institutional or departmental research projects
- Communicate project status and improvement areas to leadership
- Support investigator-initiated protocol development, including protocol writing, case report form development, budget development, and departmental research committee coordination
- Provide guidance on project planning, logistics, and implementation
- Implement and coordinate department-wide research quality management or clinical trial recruitment initiatives
- Ensure compliance with federal and local agencies, including the FDA and local Institutional Review Board
- Maintain research practices using GCP guidelines
- Maintain patient confidentiality according to HIPAA regulations and applicable law
- Develop scientific documents for abstracts, publications, presentations, funding applications, and study protocols
- Serve as an internal advisor for specific departmental activities
Requirements
What you’ll need- Bachelor's degree is required.
- Five (5) years of proven experience in area of research specialty.
- Knowledge of Good Clinical Practice (GCP) guidelines
- Knowledge of FDA and Institutional Review Board compliance requirements
- Knowledge of HIPAA regulations and applicable law
Benefits
Comp & perks- Benefits eligibility for this fixed-term part-time position
- Participation in required training and education programs