Senior Manager of BioPharma and Laboratory Projects

Description

About Us

CSI Laboratories, a Fulgent Genetics Company, is a nationally recognized cancer testing and diagnostics laboratory experienced in helping pathologists and oncologists diagnose and treat cancer patients.

Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service genomic testing company built around a foundational technology platform. 

Through our diverse testing menu, Fulgent is focused on transforming patient care in oncology, anatomic pathology, infectious and rare diseases, and reproductive health. We believe that by providing a wide range of effective, flexible testing options in conjunction with best-in-class service and support, we can redefine the way medicine is managed for patients and clinicians alike.

Since integrating with our therapeutic development business, Fulgent is also developing drug candidates for treating a broad range of cancers using a novel nanoencapsulation and targeted therapy platform. By merging our fields of expertise, we aim to become a fully integrated precision medicine company.

Summary of Position

The Senior Manager of BioPharma and Laboratory Projects is responsible for developing the technical components and overseeing the day-to-day operations of the BioPharma Division. This position will require collaboration between the managers and medical practice for each technical area. The Senior Manager is responsible for the oversight of staffing and budgetary considerations of the BioPharma Division. This position will adhere to project guidelines ensuring timely communication of adverse events and maintaining stated turn-around times. This position will also assist with laboratory projects as necessary. An understanding of the laboratory and BioPharma workflows, logistics, and clinical principles of laboratory testing are required.

Key Job Elements

• Management oversight of all BioPharma operations for the laboratory as they pertain to Accessioning, Flow Cytometry, Genetics, IHC/HIS, and Molecular technologies.
• Oversee the implementation of a new LIS for the BioPharma Division.
• Oversee and coordinate new projects within the laboratory and Biopharma operations space.
• Assist with and participate in the inspection and review process from CAP, CLIA, or other accrediting agencies for the laboratory.
• Responsible for ongoing development of managers and frontline teammates.
• Must collaborate with individuals at other sites to ensure company initiatives are successfully executed.
• Manage, in coordination with each department manager/supervisor, the staffing model and staffing utilization to maintain and improve efficiency, productivity, and overtime usage.
• Lead or assist with projects and project management as assigned.

Qualifications

Knowledge/Experience

• BS in a laboratory science or BA in administration.
• Minimum of 8 years of BioPharma laboratory management experience.
• Laboratory personnel participating in licensure or certification maintenance programs must complete the number of continuing education hours prescribed by their licensing or certifying agency.
• Technical laboratory personnel whose certification has been grandfathered and does not require participation in a certification maintenance program must complete at least twelve hours of continuing education annually.

Environment

Fulgent Therapeutics LLC/CSI is an Equal Employment Opportunity Employer. The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. The term “qualified individual with a disability” means an individual with a disability who, with or without reasonable accommodation, can perform the essential functions of the position.

• Adherence to standard universal precautions. Exposure to biological and chemical hazards