clinical case manager salaries in los angeles, california

job summary: Seeking a highly motivated Senior Scientist, Analytical Development, reporting directly to the Head of Process Sciences, to lead a multi-functional laboratory team developing analytical (molecular, bioassays, and immuno-assays inclusive) assays to support the development of novel modified autologous and allogeneic cell/gene therapies. This role will be responsible for preclinical and clinical assay development / optimization / qualification to support required testing of cell / gene therapies and viral vectors used in the manufacturing process. Additionally, some support of testing components and raw materials with contract laboratories may be required. The successful candidate will have extensive experience with cell/gene therapy analytical assay development, deep expertise on the underlying science and technology of these assays, and a detailed understanding of the CMC testing requirements for IND / NDA filings, and materials qualification. This position represents a seasoned people leadership skillset, and the energy and boldness to grow an innovative assay development laboratory organization. The successful candidate has demonstrated experience in the cGMP method qualification/validation requirements for phase-appropriate cell-based therapies. Hours: 8:30- 5:00   location: Covina, California job type: Permanent salary: $125,000 - 140,000 per year work hours: 9 to 5 education: Masters   responsibilities: Expert in analytical assay development adopting the quality-by-design concept to support testing of all pre-clinical and clinical cell therapy programs.Provide strategic and scientific guidance in all analytical development technical areas; Serve as the analytical development expert on molecular/ biological/ immuno-assays, structure-function relationships, test method development and qualification/ validation, and establishment of specifications, including cell and gene therapy programs.Oversee all analytical development personnel and activities, including laboratory. equipment/instrumentation, execution of testing, and data interpretation of results.Develop method platforms to support current and new product formats, increased product control, lower cost, and lower operational laboratory complexity.Work strategically to accelerate the development and implementation of novel testing technologies for integration into new and existing drug products.Play a key role in project team meetings and decisions working closely with other functions such as Research, Regulatory Affairs, Manufacturing, Quality, Clinical, Finance, Program Management, Business Development, and others.Prepare and present to leadership, external clients, and stakeholders on analytical method development strategy, latest data and conclusions, plans and roadmap to meet client and company testing development goals.Responsible for method LCM; execute on IND development timelines against operational plans.Builds a strong scientific and technical laboratory team, provides necessary training and ongoing coaching, discipline, and recognition of direct staff, including performing annual performance reviews.Support technology transfer of products and processes into the cGMP facility, and serve as a key SME with external laboratory organizations and key clients as well as material/component and equipment/instrument vendors.Investigate and resolve problems, identify root cause, and propose laboratory operation improvements through clear communication to senior management.Interact with outside vendors and senior management.Participate in multi-functional project teams, as necessary.Take corrective action to bring about required changes using approved change control procedures.  qualifications: Master's / PhD degree in Biochemistry, Cell Biology, Molecular Biology, Virology, Biological Sciences with 5 - 8 years of experience managing a technical laboratory team in the cell therapy biotechnology industry.Direct experience with cell and gene therapy process development, IND filing, and supporting clinical products expectations is required.Two (2) - three (3) years managing an analytical science or multi-functional bioanalytical laboratory technical team.In-depth experience and knowledge in biotherapeutics analytics with emphasis on cell-based potency methods, cellular characterization, viral characterization and infectivity assays, molecular methods, antigenicity methods, and other separation-based methods used for gene/cell therapies.Familiar with the FDA regulatory requirements for drug products and IND filingKnowledgeable of cGMP processes and technology transfer.Demonstrated ability to design and execute laboratory experiments and evaluate data to provide scientific guidance on assay optimization.Demonstrated ability to technically trouble shoot and resolve assay challenges to successfully produce cell therapy products at a high-performance rate.Demonstrated ability to develop, qualify/validate and transfer biologics analytics into manufacturing processes and product testing that meet customer needs is required.Knowledge of method lifecycle management - from early to late-phase and throughout commercialization.Knowledge of cGMP in the pharmaceutical industry. Application to cell/gene therapy and viral vector development/manufacturing a plus.Familiar with data analytics software such as JMP, Minitab, and/or GraphPad Prism.Must have strong interpersonal and communication skills, be a team player and be willing to work in an environment where individual initiative, accountability to the team, and professional maturity are required.Strong problem-solving and organizational skills are required.   skills: Molecular Biology, Cell Biology, Assay Method, Immunoassays Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.

job summary: Join a fast-paced and rapidly growing biotech start up! Here, you will contribute your talents in a purposeful way that impacts the lives of patients around the world. You will be supporting the development and manufacturing of cell and gene immunotherapies for the treatment of cancer and rare diseases, in a state of the art facility. Position Summary: We are looking for an enthusiastic Researcher with either academic or industry experience to assist with genetic engineering of lentiviral vectors expressing antibodies and CAR and in vitro assays. The candidate will focus on the Discovery of Antibody based biologics and T/NK cell products as well as assist with planning and execution of experiments, in support of developing analytical methods for releasing and characterizing T cell therapy products. Candidates with strong expertise in phage display library construction and antibody engineering will be given preference. The successful candidate will demonstrate a strong sense of responsibility, open communication, desire to learn new skills, ability to meticulously perform instructed tasks and maintain lab records. S/he will perform bench work to support research projects in coordination with our scientific director. We are looking for enthusiastic individuals with a flexibility to adapt to startup environment. Hours: 8:30 AM - 5:00 PM   location: Covina, California job type: Permanent salary: $100,000 - 130,000 per year work hours: 9 to 5 education: Masters   responsibilities: Use expertise in molecular biology to generate Chimeric Antigen Receptor (CAR) or antibody constructs.Engineer lentiviral vectors with insertion or deletion of restriction sites, epitope tags or other genetic elements.Generate viral vectors expressing scFv or CAR variants, site directed mutants, and fusion proteins using fusion PCR and Gibson or other fragment assembly methods.Design and clone shRNA, gRNA for desired targets in CRISPR / Cas9 vectors.Design strategies to knock-in CAR in T cells(4) Perform antibody phage display screens and validation of clones by ELISA and flow cytometry.Express/Purify antibodies and recombinant proteins in bacteria or mammalian cells.Develop biochemical, cell based and immunoassays to evaluate antibody binding affinitiesOptimize qPCR / ddPCR assays to characterize viral and CAR-T products.Construct phage display librariesPerform restriction analysis, ligation, transformation, colony PCR screens and gel electrophoresis.Develop generate stable cell lines with overexpression or knock out (CRISPR shRNA).Prepare plasmids in small scale and large scale, maintain plasmid and bacterial glycerol stocks.Maintain cell lines, prepare cell banks (adherent and suspension cell lines) as required.Perform cytokine ELISAs and Western blotting.Perform cell-based (proliferation, cytotoxicity, transcription factor reporter) assays in multi well formats, analyze and clearly document data.  qualifications: Ph.D in the field of Immunology, Cell biology, Virology or Cancer biology or related life science discipline with 2-8 years ORMaster's degree with 7-13 years relevant research experience in Immunology/Cancer biology.2-3 years of direct experience working on projects related to immunology (preferably immunotherapy) is required.Experience in phage display library construction, antibody engineering, humanization or affinity maturation of antibodies are preferred.Strong technical skills in advanced molecular cloning and fragment assembly techniques are requiredStrong experience in cell based and biochemical assays are required - must be able to perform assays in 96 and 384 well formats with different formats without confusion.Experience in working with multiple cell lines (both suspension and adherent) and setting up cell-based assays.General lab experience in operating and maintaining basic lab equipment (centrifuge, microscope, PCR machines, nanodrop, DNA and protein electrophoresis systems).Hands on experience with sterile microbiology and molecular biology techniques not limited to cloning, mutagenesis, restriction digestion, ligation, transformation, colony PCR, culturing bacterial cells, plasmid preparations.Critical to have the ability to maintain accurate records and back track samples prepared without confusion.Prior experience in optimizing and trouble-shooting qPCR and ddPCR Working Conditions: Laboratory environment - required to work with tumor cell lines, bacteria, phage and lentivirusMust wear PPE due to safety requirements in designated lab areasMay be required to work in controlled or clean room environmentsExpected to work safely and effectively when working alone or working with othersTravel: Occasional. Less than 3%Occasional stooping, bending, stretching, pushing, pulling, reaching and/or lifting up to 40lbs.Ability to sit, stand, walk, and move within workspace for extended periods.Ability to perform repetitive tasks including hand to finger manipulations, grasping, pushing, and pulling. Environmental Conditions:Primarily office environment but will be required to enter laboratory or GMP process areas donning proper gowning / lab coats or PPE such as safety glasses and shoes.Ability to work safely and effectively when working alone or working with others.  skills: Molecular Biology, Cell Biology, PCR, SOP, GLP (Good Laboratory Practice), Immunoassays, Flow Cytometry Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.

job summary: Rapidly growing Engineering, Design and Manufacturing company is currently in search for a Design Project Manager to join their team. The ideal candidatee have a B.Arch/M. Arch with 7+ years of experience managing design process for projects in Los Angeles. The role will be client-facing, managing/meeting deadlines, and in correspondence with design stakeholders throughout the preconstruction process.   location: CARSON, California job type: Permanent salary: $100,000 - 120,000 per year work hours: 8am to 4pm education: Bachelors   responsibilities: Expertly reviewing contract documentation to ensure fabrication drawings meet all A/EOR specifications.Managing the collaboration with A/EORs throughout preconstruction by channeling internal resources provided to the project.Managing multiple projects at a time, building design schedules, and communicating effectively to all necessary parties as req'd.Supporting design assist initiatives in contracts early stages. #LI-AS1   qualifications: Experience level: ExperiencedMinimum 5 years of experienceEducation: Bachelors (required)  skills: Design Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.