87 clinical case manager jobs found in california

job summary: Sr. Manager, Clinical Supplies (Oral Solid Dose) 6 Month Contract (may extend or convert) Remote (75%) + 1 week / month in South SF Looking for West Coast Based Candidates (travel reimbursed) Must Have: Experience with oral tablet dosage form Phase 1 & Small Biotech experience APAC logistics experience is a plus Strong MS Excel skills Seeking a talented, independent, and highly motivated Senior Manager, Clinical Supplies Planning

job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. As the world's leading provider of diagnostic information services, our client is committed to sharing our

job summary: Sr. Pharmacovigilance (PV) Operations Manager | Remote | West Coast This critical role is responsible for managing and overseeing PV operations across clinical development programs, ensuring seamless collaboration with PV vendors. You will play a key role in preparing for the initiation of two global Phase 3 trials, ensuring all PV activities are in place. Your expertise in global trial management, study document review, and vendor oversight

job summary: We are seeking a Sr. Data Analyst to join the Clinical Systems Analytical & Reporting (CSAR)-Analytics team within Global Development Operations. This role will enhance our analytical reporting capabilities and support business continuity across multiple clinical system technology enhancement projects. Key responsibilities include contributing to analytics initiatives supporting critical business functions relying on data from eTMF, EDC, CTMS

job summary: We are seeking a Clinical Site Contracts Specialist to manage end-to-end processes for clinical site contracts and consulting agreements, ensuring smooth study start-up and trial operations. If you're detail-oriented, proactive, and passionate about negotiation and collaboration, this is your chance to contribute to critical clinical research initiatives. Apply today to take the next step in your career-let's start the conversation! locati

job summary: The Real World Evidence Leads are part of the Medical Evidence Generation function comprised of subject matter experts in evidence planning, study design and data interpretation. The function works to drive excellence in evidence planning and implement novel study design approaches to generate robust evidence to enhance understanding of unmet medical need; support patient and endpoint selection for Clinical studies; and inform clinical practi

job summary: Global Regulatory Policy and Intelligence engages regulators, industry and professional associations, and patient advocates externally and subject matter experts across the Company to advance important Regulatory policy issues aligned with Company's goals and priorities. It also manages Regulatory Intelligence for the Global Regulatory Affairs organization, enabling fast, efficient global filings by effectively monitoring, analyzing, and comm

job summary: Immediate opening for a QA Frontline Associate (Night Shift) to support the Technical Operations team at a leading, global pharmaceutical company specializing in rare diseases. The Technical Operations group is responsible for creating drugs for use in clinical trials and for scaling production of those drugs for the commercial market. The QA Frontline team is committed to providing real time QA support to the manufacturing facilities by perf

job summary: A R&D Packaging Engineer for a medical devices and equipment manufacturing company is needed in the Fremont, CA area. This role involves leading the design, development, and compliance of medical device packaging and labeling solutions while collaborating cross-functionally to support EU MDR implementation, drive continuous improvement, and manage projects in a regulated environment. location: Fremont, California job type: Contract salar

job summary: The Associate Quality Systems Specialist will be part of the Quality team and responsible for providing quality support for the site quality management system. This position ensures compliance of the quality system with regulations relevant to the business, including but not limited to, ISO13485, MDSAP, IVDD/IVDR, CFR 21, GxP, and the quality manual. This position is multi-disciplinary with opportunities to work on future products and current

We are seeking a detail-oriented Order Management Specialist to join our team. You will be responsible for ensuring seamless order processing and exceptional customer service for our luxury hotel and retail clients, working with premium gourmet food products.Key Responsibilities: Order Accuracy: Process orders with 100% accuracy, including product details, labeling, shipment methods, and delivery timelines. Urgency & Efficiency: Prioritize urgent r

job summary: We are seeking a Regulatory Submission Manager to support global regulatory initiatives and ensure compliance with regulatory requirements for investigational and marketed products. Role involves working closely with cross-functional teams and regulatory leads to support submission activities, labeling development, and strategic regulatory guidance. The ideal candidate has a strong background in regulatory submissions and document review, as

Do you have a passion in assisting patients regardless of their income or insurance status? If so, we are seeking for a Front Desk Receptionist who will provide administrative duties that will complete patient registration including entering patient demographics and payer/insurance information into an EMR system. Hours will be 8am-5pm M-F salary: $21 - $23 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: High SchoolResponsibilitiesRandsta

"Passionate about food safety and quality? Join our team and play a key role in ensuring our products meet the highest industry standards! If you have an eye for detail, a commitment to excellence, and a drive to make a real impact, this is the opportunity for you!" About the Role: We are seeking a detail-oriented Quality Assurance Technician to join our team. In this role, you will be responsible for ensuring that our food products meet the highest stand

job summary: Seeking a talented and motivated individual with expertise in enzymology and biochemical assay development to support small molecule drug discovery. The successful candidate should possess strong technical expertise & exceptional hands-on laboratory skills, have excellent written and oral communication skills, enjoy working in a fast-paced multi-functional team environment, and keep current with field of expertise, including literature and te

job summary: Let's do this. Let's change the world. Company's research Technology department seeks a Scientist who supports our Emerging Modalities group. In this interdisciplinary role, you will join a fast-paced, cross-functional product team focused on discovering new treatment strategies for human diseases. Key Skills: Recent cell culture experience, plate based assays, imaging experience, flow cytometry.Transfection, Transduction, cell EngineeringP

job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their bus

job summary: The Associate of Manufacturing will work in a dynamic production environment at the Company Thousand Oaks Site supporting development, clinical, and launch activities.Under general supervision, employee will perform operations in the Manufacturing area.Operations will be performed according to Standard Operating Procedures (SOPs). location: Newbury Park, California job type: Contract salary: $28.00 - 30.36 per hour work hours: 7

job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve t

Are you detail-oriented with a passion for accuracy and compliance? We are looking for a Document Specialist to join our team! In this role, you'll play a vital part in ensuring smooth patient care by collecting, verifying, and managing crucial medical documentation. ✨ Why Join Us? ✅ Stable Work Schedule – No weekends! Enjoy a Monday-Friday, 8:00 AM – 5:00 PM schedule. ✅ Competitive Pay – Earn $19.00/hr while making an impact in he

job summary: This Laboratory Operations role in Temecula, CA, is ideal for a life science professional with a bachelor's degree or 3-5 years of relevant experience. You'll be crucial in manufacturing products, performing diverse lab operations, and ensuring compliance with cGMP and regulatory standards. The position requires strong aseptic technique, experience with lab equipment, and proficiency in data entry and reporting. You will contribute to process

job summary: We are seeking a detail-oriented and collaborative Engineering Laboratory Technician to join our research and development team. 1 year Contract!! 2nd shift: 2pm-10:30pm (Monday-Friday) Required: High School Diploma or Associate Degree with 2+ years of relevant experience, or equivalent work experience.Lab experience preferred; exposure to an R&D environment is a plus.Proficiency in computer skills is a plus.Ability to work effectively

job summary: We are seeking a motivated and detail-oriented Entry-Level Biologics Development Technician to join our dynamic biologics development team. This position will play a crucial role in supporting the routine process across our Bioseparation and Cell Culture teams. The successful candidate will be responsible for various tasks related to buffer generation, solution preparation for downstream purification processes, and media formulation for cell

job summary: In this role leverage your expertise in safety, industrial hygiene, and environmental science to proactively identify, analyze, and resolve complex HSE issues in a manufacturing environment. Required: Bachelor's or Master's degree in Chemical Engineering, Industrial Hygiene, Environmental Science, or a related discipline. Minimum of 5 years of HSE experience in a manufacturing environment involving hazardous chemicals and gases. P

job summary: This is an 18-month onsite contract role based in Thousand Oaks, CA, with potential for extension. The position supports Drug Product Quality Assurance by providing daily compliance oversight on the manufacturing floor. Key responsibilities include batch record review, SOP approvals, MES and Maximo system updates, and minor deviation/CAPA record approvals. The role requires a detail-oriented team player with quality experience and the ability

job summary: Under general supervision, this position will perform routine procedures and testing in support of the lab. location: Newbury Park, California job type: Contract salary: $24.00 - 27.32 per hour work hours: 9 to 5 education: High School responsibilities: Performing routine laboratory proceduresRoutine analytical testingDocumenting, computing, compiling, interpreting, and entering dataMaintaining and operating specialized equ

job summary: The Sr. Associate Quality Assurance position supports Company's Quality Assurance program under the Plant QA organization providing daily oversight of the Drug Product manufacturing areas. Under general supervision, the role provides support and compliance oversight to Manufacturing and Facilities and Engineering staff in the execution of their processes, procedures, and use of quality systems. location: Newbury Park, California job type:

job summary: Perform experiments, organize data and analyze results under minimal supervision. With minimal supervision, plans, conducts or monitors experiments, records and organizes data, analyses results, generates robust and reliable data and/or Ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. 90% lab work including sample isolation, drying, and testing location: New

job summary: The Staff Quality Engineer, Software will be the subject matter expert on providing guidance to the organization and the software teams in establishing policies and procedures for Software Design Control. This individual will be an integral part of the software development life cycle process in informing, guiding, and evaluating the teams' adherence to practices that would ensure compliance to required regulatory requirements. SKILLS REQUIRED

job summary: Join a leading biopharmaceutical company in Thousand Oaks, CA, for an immediate opening as a Quality Assurance Associate. This is an excellent opportunity to contribute to a successful and growing organization. location: Newbury Park, California job type: Contract salary: $25.00 - 30.36 per hour work hours: 9 to 5 education: High School responsibilities: Under general supervision, this position is responsible for sampling a