- job summary: Primary point of contact to lead, manage and coordinate, in partnership with the ContractResearch Organization (CRO), the conduct of clinical trials from study design to close out at a global level in accordance with ICH-GCPOversee the quality and scientific integrity of clinical operations for studies at a global levelCollaborates with cross functional stakeholders to ensure timely and on budget execution of clinical trial deliverablesjob summary: Primary point of contact to lead, manage and coordinate, in partnership with the ContractResearch Organization (CRO), the conduct of clinical trials from study design to close out at a global level in accordance with ICH-GCPOversee the quality and scientific integrity of clinical operations for studies at a global levelCollaborates with cross functional stakeholders to ensure timely and on budget execution of clinical trial deliverables
- 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, CTMSjob 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: As a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a global leader in biotechnology. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the healthcare and life sciences industries. This company is dedicated to discovering and developing innovative therapies that address serious diseases, with a focus on oncojob summary: As a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a global leader in biotechnology. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the healthcare and life sciences industries. This company is dedicated to discovering and developing innovative therapies that address serious diseases, with a focus on onco
- job summary: As a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a global leader in biotechnology. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the healthcare and life sciences industries. This company is dedicated to discovering and developing innovative therapies that address serious diseases, with a focus on oncojob summary: As a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a global leader in biotechnology. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the healthcare and life sciences industries. This company is dedicated to discovering and developing innovative therapies that address serious diseases, with a focus on onco
- 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 abilityjob 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: 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: 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: 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! locatijob 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: 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 commjob 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: 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: 7job 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: 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 equjob 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: 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 ajob 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
