Come join our team! This role will have responsibilities promoting activities and services associated with the Cedars-Sinai Board of Governors Innovation Center and associated Cedars-Sinai laboratories in the Pacific Design Center. In particular, the Program Administrator will work with Professor David Rowitch, MD, PhD to promote cutting edge transcriptomic and proteomic analysis for insights into human diseases.

The Research Program Administrator works with the Principal Investigator or Department Head to coordinate all aspects of building a research program. This will included, development of infrastructure, overseeing clinical research staff, quality assurance, and coordination of grant activities and grant proposals. Administrator will identify improvement areas, prepare policies, train staff, and audit procedures to create an efficient clinical research program

What are the Primary Duties and Responsibilities?

• With the Principal Investigator or Department Head, coordinates all aspects of building a research program including the development of infrastructure and new research programs.
• Oversees an entire research program or group of Clinical Research Coordinators, Clinical Research Assistants, Clinical Research Associates, and/or Research Nurses.
• Oversees research Quality Assurance and Quality Control within their department or division.
• Coordinates grant activities pre award through closure (monitoring budgets, compliance, progress reports).
• Identifies process improvement areas to assure an efficient and robust clinical research program.
• Data compilation, assists with grant proposals, protocol development, scientific publication preparation, and presentations.
• May train junior research staff members.
• Involved in centralized activities such as auditing and preparation of clinical research policies and standard operating procedures.
• 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.

Qualifications:

• Bachelor's Degree preferred.
• Five (5) years of directly related experience required.
• Certification in clinical research (ACRP or SOCRA) preferred.
• Ability to use discretion and maintain privacy, confidentiality or anonymity.
• Previous laboratory manage experience preferred.
• Familiarity with bio-repository management, direct report management, research administration, and business operations/financial management strongly preferred.

Tentative Work Schedule:

• Monday - Friday 8:00am - 5:00pm