Laboratory Manager
Shirley Parsons Ltd
Shirley Parsons has been retained by the University of California, Los Angeles, to seek a Biosafety Manager to lead its biological safety and high-containment programs on campus. The Biosafety Manager will act as the campus Biosafety Officer (BSO), which serves as the campus subject matter expert for biological safety/biosecurity at UCLA. The Biosafety Manager will be ex-officio member of the UCLA Institutional Biosafety Committee (IBC) and is tasked with advising the committee on best management practices for mitigating biological hazards. The Role Act as the Alternate Responsible Official to the High Containment Director and Associate Biosafety Officer for the Select Agent Program; Support and oversee the High Containment Director in managing the BSL-3 facilities & operations; Support and oversee the Vivarium Safety Officer in providing safety services to vivarium staff and researchers working with animals and plants; Set schedules and assignments of biological use authorization reviews; Set inspection assignments of laboratories with biological hazards including animal biocontainment facilities; Serve as the primary biosafety subject matter expert, advising stakeholders and supporting institutional committees on best practices Function as point of contact during regulatory inspections (NIH, CDC USDA, etc.); Review and manage the campus medical waste program; Provide input for Research Safety Plan Reviews; Manage biosafety training development; and Develop and maintain campus documents and policies such as the UCLA Biosafety Manual, Exposure Control Plans, Standard Operating Procedures/Policies, etc. The Candidate Minimum 7 years of relevant experience in biosafety, including management of BSL-3 or higher containment facilities and working with infectious agents, human gene transfer, recombinant and/or synthetic nucleic acids. Demonstrated leadership experience overseeing professional staff in a highly regulated environment, including mentoring and performance management. In-depth knowledge of NIH Guidelines, Cal/OSHA Bloodborne Pathogens Standard, Cal/OSHA Aerosol Transmissible Disease Standard, and federal select agent regulations. Experience working with vivarium operations and high-containment environments, managing risks associated with animal care, zoonotic diseases and infectious agents. Ability to establish and maintain cooperative working relationships with otherstaff members, administrators, managers, subordinates and academia. Ability to analyze complex technical data from environmental surveys, using logic and quantitative reasoning. Ability to make oral presentations, lead meetings, with persons of various social, cultural, economic, and educational backgrounds to persuade others to accept a specific action or opinion, and also to provide information to explain procedures, policies, etc. Skill in writing grammatically correct, concise and accurate communication for the purpose of training, inspection, gathering and dissemination of information relevant to biosafety. Demonstrated experience in coordinating and delegating tasks with various groups to meet common goals. In-depth knowledge of NIH Guidelines, Cal/OSHA Bloodborne Pathogens Standard, Cal/OSHA Aerosol Transmissible Disease Standard, and federal select agent regulations. Demonstrated experience in coordinating and delegating tasks with various groups to meet common goals. Bachelor's Degree Microbiology, biology, industrial hygiene or related biological science or safety disciplines or equivalent experience / training Or Master's Degree Advanced degree (Master’s or PhD) is preferred but not required in biological sciences, microbiology, or related field or equivalent experience / training. Current professional biosafety registration or certification (RBP or CBSP, respectively) or eligibility for certification is strongly preferred. #J-18808-Ljbffr
- ...StatesCompany: Providence Health & ServicesPosted: 2026-08-12Providence St. Joseph Medical Center in Burbank, CA is seeking a Senior Medical Laboratory Scientist for a full-time role with 8-hour, variable shifts. The incumbent will assist the Clinical Specialist in supervising a...SuggestedFull timeShift work
- ...edge technology. We help our clients envision and achieve Digital Laboratory Transformation through co-creation and application of digital... ...scientific user experience to help our clients better capture, manage, integrate, and analyze complex scientific data. We help...SuggestedLive inWork at officeLocal area
$110k - $120k
...Competitive pay and great benefits! AOCUSA pays the full cost of our Employee's Health Insurance We are looking for a Senior Laboratory Manager for the following shift: First Shift: 6:00 AM – 2:30 PM Full-Time: Monday – Friday + mandatory weekends at the...SuggestedFull timeSeasonal workWork at officeMonday to FridayShift workWeekend workDay shift- ...Clinical Laboratory Scientist/Lab Manager Golden Star Labs is leading the industry in science and innovation to better support communities and institution's testing needs across the United States. We are looking for an experienced CLS with a microbiology or generalist...SuggestedWork at officeFlexible hours
- ...implementation of standard and non-standard quality control and/or assurance measures and documents feedback to research staff and management. Supports and develops materials for the education of research staff and/or participants on protocols, documentation procedures,...SuggestedFor contractorsFor subcontractorLocal area
- ...MLK Community Healthcare in Los Angeles seeks a Laboratory Manager reporting to the Director of Laboratory Services to oversee the daily operation of the clinical laboratory. You will ensure compliance with CAP, AABB, FDA, OSHA and JCAHO, manage staff, quality assurance...
$86.4k - $184.8k
...Work (CREW) Clinical Research Coordinator Supervisor is an experienced professional responsible for overseeing, coordinating, and managing complex investigational drug clinical trials, as well as supervising other clinical research coordinators. This role involves close...Full time$31.51 - $62.64 per hour
...Description The Project Manager (PM) for the Division of Clinical Trials Development (CTD) supports clinical research efforts at UCLA and within the TRIOUS Network. Under the direction of the CTD Manager, investigators, and Senior Management, the PM contributes to protocol...Hourly payLocal areaShift work- Job TitleClinical Research Coordinator IIJob DescriptionThe Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating...Local area
- Job TitleClinical Research CoordinatorWork LocationSanta Monica, CA, USAWork ScheduleOnsite or Remote Flexible Hybrid Work Schedule Monday – Friday, 8:00am - 5:00pmSalary Range$38.19 - 61.45 HourlyJob DescriptionBachelor's degree in related area and/or equivalent combination...Local areaRemote workMonday to FridayFlexible hours
- ...of clinical research studies, ensuring compliance with all regulatory guidelines. This position involves screening participants, managing study documentation, and supporting study procedures to ensure smooth operations. This is an onsite, contract opportunity offering...Contract workWork at office
- Innovo Research is seeking a Senior Clinical Research Coordinator to coordinate daily operations for studies at our partner site. You will supervise staff, ensure protocol compliance, and support regulatory submissions while maintaining high quality data and subject safety...
$92k - $100k
...ManagerThe Department of Psychiatry and Behavioral Sciences at the University of Southern California is seeking a Clinical Project Manager to support NIH- and foundation-funded clinical research programs focused on behavioral health, substance use, and mental health intervention...Work experience placementLocal area- ...center environment. Familiarity with industry-sponsored clinical trials and sponsor interactions. Additional Information Budget management experience is not required. NIH and multicenter trial experience are preferred but not required. Candidates with experience in academic...
- A leading healthcare institution in Beverly Hills is seeking a Clinical Research Coordinator II to manage study coordination, including patient screening and data management. The role involves ensuring compliance with regulatory standards and efficiently reporting study...Work at office
- ...Responsibilities Partner with Regional Site Director to ensure compliance and productivity of all clinical site staff and operations. Manage, train and support clinical site staff. Review, comprehend and communicate study protocols. Oversee Site Initiation Visit (SIV),...Full timeInterim role
$93.93k - $151.1k
...Description The Senior Clinical Research Coordinator plays a critical role in the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The ideal candidate is an experienced professional or leader who...Local areaFlexible hours$51.23k - $70.44k
...exclusion criteria. Liaises with agencies, pharmaceutical companies, laboratories, vendors, equipment, and supply companies as needed; oversees availability of supplies and/or equipment for studies. Manage multiple concurrent trials - screening, recruiting, and enrollment...Full timeCasual workLocal areaWork visaShift workAfternoon shift$120k - $150k
...Generous PTO Industry leading benefits Company Vehicle 401(K) Job Details Job Details Are you an experienced Project Manager with a background in civil construction? Do you have a passion for leading complex projects, estimating costs, and ensuring that...Permanent employmentFor contractorsFor subcontractorLocal area- ...providing administrative support to the clinic. Working on behalf of the Principal Investigator (PI), this individual independently manages the full study lifecycle—from feasibility and start-up, through patient recruitment, eligibility assessment, and follow-up, to the...Work at officeFlexible hoursNight shift
- The University of California - Los Angeles Health is seeking a CLS to coordinate activities in the Clinical Laboratory, overseeing pre-analytical, analytical, and post-analytical processes. The role requires a valid California CLS License and a minimum of four years of...
$54.02 - $86.43 per hour
...partnership with HSU and AHS leadership the CLS Program Director will manage the recruitment and selection process of incoming students and... ...clinical expertise and can perform the duties of a Clinical Laboratory Scientist III. Teamwork/Customer Relation Responsibilities...Remote workShift work- ...Beverly Hills is seeking a Clinical Research Coordinator II for a hybrid role. This position involves coordinating clinical studies, managing patient interactions, ensuring compliance with FDA regulations, and maintaining accurate research documentation. Candidates should...Local area
$62.4k - $83.2k
...clinical team to ensure the highest standards of data integrity, patient safety, and operational excellence. Job Duties Study Management: Serve as the primary or co-coordinator for assigned Phase II/III clinical research studies, overseeing day-to-day operations...Hourly payFull time- ...Clinical Practice (GCP) guidelines. Draw, process, and ship laboratory specimens, including the handling of dangerous goods, in... ..., and healthcare environments. Strong organizational, time management, and attention-to-detail skills with the ability to manage multiple...H1bWork at officeMonday to Friday
$30.74 - $49.46 per hour
...Description The Assistant Clinical Research Coordinator (ACRC) contributes to the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The position has responsibility for the coordination of research...Hourly payLocal areaFlexible hours$27 per hour
Clinical Research Coordinator I Inglewood Clinical is part of the Irvine Clinical Research site network, the largest of its kind on the West Coast. With 5 research centers in California, we are leaders in the search for new treatments in neurology, psychiatry, and obesity...Full time$31.51 - $62.64 per hour
...Description The Project Manager (PM) for the Division of Clinical Trials Development (CTD) supports clinical research efforts at UCLA and within the TRIO-US Network. Under the direction of the CTD Manager, investigators, and Senior Management, the PM contributes to...Hourly payFull timeShift work- ...Description The Senior Clinical Research Coordinator contributes to the overall operational management of clinical research/trial/study activities related to research activities in the Department of Urology Center for Pelvic Health and Wellness. The incumbent will...Full time
- ...Coordinator to support interventional clinical trials across multiple divisions. This role will be responsible for coordinating and managing study activities for both drug and device trials, including participant recruitment, study implementation, data collection, and...Hourly payFlexible hours
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