clinical case manager salaries in los angeles, california

job summary: We are the #1 HR Services Company in the world and we are sourcing for a Sr. Research Scientist in the greater Los Angeles, CA area. The ideal candidate will be passionate about ensuring the sound science of our nutrition products, along with developing relevant and meaningful product and program solutions that address key customer needs in the health and wellness space. This is a direct hire position and can start immediately.   location: Buena Park, California job type: Permanent salary: $115,000 - 130,000 per year work hours: 8 to 4 education: Masters   responsibilities: What's special about this team: The Health Seekers Platform is a cross-functional product development team comprised of formulation, process engineering, package engineering, and nutrition investigations. The team's work focuses on innovation and delivery of new products for our targeted product platform and the 40+ age segment -vision health, bone health, immunity, etc. Working with this technical team, you will develop with an open innovation mindset, working both internally and through external partnerships to offer creative & engaging product offerings. Your teamwork will continue to position the team as the leading direct selling company in the world by offering innovative product solutions for our targeted nutrition category. You will add energy and inspiration to a strong technical team! What's special about this role: As a Senior Nutrition Research & Clinical Investigator on this team, you will evaluate scientific research to support the Nutrilite global product portfolio and provide scientific credibility to differentiate Nutrilite products from competitors. Your role will require you to work on front end research, helping to identify relevant mechanisms of action and outcomes, and to partner with internal teams and/or external partners to advance ingredient and product technologies. If clinical studies are warranted, you will develop protocols, identify the appropriate CRO or academic partner, oversee study execution and results analysis, and then translate the results into consumer-friendly and regulatory acceptable claims and stories which support the efficacy of our products. Your background in both nutrition science and clinical research will be showcased in the role. Your work will maintain the high credibility of the Nutrilite brand and will offer a highly visible role, providing patent and publication opportunities, in addition to the ability to travel globally, meeting and sharing expert insights about Nutrilite products, nutrition, and health. If you have a passion for health and wellness, enjoy translating complex nutrition science into efficacious, experiential products, and the ability to share your expertise with clients and customers around the world, this role can offer a strong platform to spotlight your talent!   qualifications: Required qualifications: Minimum 3 - 6 years of experience in nutrition research and product claim substantiationAdvanced degree (MS or PhD) in Bioscience, Nutrition Science, or related scientific disciplineProven exposures incorporating functional botanicals and botanically derived bioactives into product profile designAbility to translate complex scientific and technical concepts into consumer appropriate language, ideally with compelling visuals, to enable communication and understanding of the science underlying the productInterpersonal skills to influence and inspire both internal and external audiencesExperience leading clinical studies in an industry setting is helpfulBasic understanding of global regulations in the nutraceutical industry is preferredIndustry awareness with knowledge of trends and innovation desiredRD (Registered Dietician) Certification, ACRP (Association of Clinical Research Professionals) Certification, or naturopathic background helpful  skills: Biology, Food Product Development 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.EOEDisclaime 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: The Regulatory Specialist position provides regulatory document support to the Kaiser Permanente Northern California (KPNC) principal investigator and research sites conducting multiple FDA-regulated or other clinical trials. The regulatory specialist position provides operational support for regulatory compliance. This position works in consultation with the principal investigator, sub-investigators and teams members. This position Is also responsible for assisting in protecting the health, safety, and welfare of research participants. This position is a non-licensed position which must adhere to the position's scope of practice. Requirements: Bachelors Degree RequiredMust be proficient in word-processing, spreadsheet, and database softwareDemonstrate excellent written, verbal, and interpersonal communication skillsAbility to read and comprehend complex study documents and summarize key components in a succinct mannerAttention to detail and accuracy.Ability to manage multiple tasks with strict timelines.Demonstrate prioritization and organizational skills.Ability to address issues with problem solving skillsAbility to work effectively on cross-functional teamsBasic knowledge of the principles, methods and procedures of basic medical and/or clinical research processes.Basic knowledge and understanding of human research protection regulations, policies, procedures, and standards as applied toIRB and compliance operations'   location: Pasadena, California job type: Contract salary: $48.79 - 54.89 per hour work hours: 8am to 4pm education: Bachelors   responsibilities: The Regulatory Specialist position provides regulatory document support to the Kaiser Permanente Northern California (KPNC) principal investigator and research sites conducting multiple FDA-regulated or other clinical trials. The regulatory specialist position provides operational support for regulatory compliance. This position works in consultation with the principal investigator, sub-investigators and teams members. This position Is also responsible for assisting in protecting the health, safety, and welfare of research participants. This position is a non-licensed position which must adhere to the position's scope of practice. Requirements: Bachelors Degree RequiredMust be proficient in word-processing, spreadsheet, and database softwareDemonstrate excellent written, verbal, and interpersonal communication skillsAbility to read and comprehend complex study documents and summarize key components in a succinct mannerAttention to detail and accuracy.Ability to manage multiple tasks with strict timelines.Demonstrate prioritization and organizational skills.Ability to address issues with problem solving skillsAbility to work effectively on cross-functional teamsBasic knowledge of the principles, methods and procedures of basic medical and/or clinical research processes.Basic knowledge and understanding of human research protection regulations, policies, procedures, and standards as applied toIRB and compliance operations'   qualifications: Experience level: ExperiencedMinimum 3 years of experienceEducation: Bachelors  skills: RegulationsFDAclinical trialHuman Resources 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. 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: This role will independently design and execute experiments, mentor technical staff, collaborate with other cross functional teams to support research projects under the supervision of R & D director. Passion for excellence and innovation are critical. This role will work closely with our internal colleagues and external collaborators to efficiently progress early-stage cell therapy products through to IND filing.   location: Arcadia, California job type: Permanent salary: $100,000 - 130,000 per year work hours: 9 to 5 education: Doctorate   responsibilities: Lead planning, design, and execution of experiments related of development and characterization of cellular immunotherapy products in coordination with R & D Director.Analyze, and report complex data to cross functional teams in a clear and concise mannerMentor and train scientific staff on technical skills required to effectively perform experiments and to facilitate progression of projectsManage multiple research projects simultaneously with the R & D team and collaborate with other departments (Process Science, Analytical Science, Quality, Manufacture) as necessary.Contribute to various preclinical projects within R& D and those required by clients through in-depth scientific knowledge and demonstrated experience in analytical methods used in cellular immunotherapy fieldCollaborate with Process science team to scale up lentiviral and CAR-T productsPerforms a wide range of non-routine exploratory experiments as requiredMaintain precise laboratory notebooks, electronic records following high standards of data quality and integrity.Prepare scientific/technical reports, summaries, protocols, etc, and present them to internal and external stakeholders.Constantly improvise research strategies and adopt technologies to stay upfront in the field of immunotherapy  qualifications: Ph. D in the field of Immunology, Cell biology, Virology or Cancer biology or related life science discipline with 3+ years (Scientist) or 5+ years (Senior Scientist) or Master's degree with 7 + years relevant research experience in Immunology/Cancer biology.In depth scientific and technical understanding of cellular immunotherapy and tumor immunology.2+ years of managing research laboratory research team/associates in immunotherapy or cancer biology or relevant research projects is required for senior scientist level.Prior research experience in antibody therapies, bispecific antibodies, and cellular therapies preferredDemonstrated ability to independently design, plan and troubleshoot experiments, interpret results, and present to the R&D team and external clients.Self-motivated and creative, able to work within a team and collaborate with external teams as needed to accomplish project objectives and deliverables.Possess ability to identify problems early, technically trouble shoot and resolve challenges in early development and preclinical validation of CAR-T productsUnderstands the importance of data integrity to enable a smooth transition of discovery research to manufacture and clinical trials.Familiarity with FDA regulation of biologics and cell therapy products, IND-filing, GLP/GMP process is a plus.Ability to stay organized, prioritize tasks, manage time efficiently, and provide creative solutions to meet program needsExcellent interpersonal, verbal, and written communication skillsComfortable working in a fast-paced startup environment and flexible to adjust workload based upon changing prioritiesA strong academic research experience evidenced by high caliber publications in peer-reviewed journals is preferredIntellectually curios candidates with passion for innovation and discovery research are welcome  skills: Biology, Chemistry, GLP (Good Laboratory Practice), ICH Regulations, GMP (Good Manufacturing Practice) 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.EOEDisclaime 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.