Job Description Summary The GCP Compliance Manager (Program & Study) is accountable for the compliance oversight... as per program/trials’ selection and GCO self-strategy delivery. The GCP Compliance Manager (Program & Study) is the single point...
Job Description Summary -The GCP Compliance Manager (Program & Study) is accountable for the compliance oversight... as per program/trials’ selection and GCO self-strategy delivery. The GCP Compliance Manager (Program & Study) is the single point...
Job Description Summary The GCP Compliance Manager (EMEA Hub) is accountable for the compliance oversight and control..., audits & inspections as per country assignment and GCO self-strategy delivery. Job Description The GCP Compliance Manager...
SSO Country Manager, SSO Country Head, SSO Feasibility Manager, SSO Study Start-up Manager and SSO Site Partnership... of assigned DEVELOPMENT studies in E2E product line Clinical Operations Program Head/Study Lead/CPM-CRA. Can be assigned partially...
SSO Country Manager, SSO Country Head, SSO Feasibility Manager, SSO Study Start-up Manager and SSO Site Partnership... of assigned DEVELOPMENT studies in E2E product line Clinical Operations Program Head/Study Lead/CPM-CRA. Can be assigned partially...
Job Description Summary Accountable for the oversight and coordination of program and study level (re-)feasibility... assessments in the country, in collaboration with program and/or trial feasibility teams, in compliance with Novartis processes...
of. Join us. QUALITY COMPLIANCE SENIOR MANAGER LIVE What you will do In this vital role you will provide proactive end to end quality... clinical development program. You will support global and local study teams and all clinical trial sites who participate...
of a clinical study under the guidance of the (A)CD(M)D in compliance with Novartis processes, ICH GCP and regulatory requirements...(s) activities to deliver study outcomes within schedule, budget, quality/compliance and performance standards. May lead specific...
compliance and delivery according to protocol, SOPs, ICH GCP and country regulations. This may include data management, study... deliverables with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity. Oversees site interactions...
compliance and delivery according to protocol, SOPs, ICH GCP and country regulations. This may include data management, study... deliverables with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity. Oversees site interactions...
like they belong. Job Responsibilities The Local Study Manager (CTM II) is accountable for the strategic planning & management... archiving, including study timelines, study budget, and study conduct in accordance with SOPs and ICH/GCP and regulatory...
of customer expectations Monitor study timelines and manage the financial components of each program/study, which includes... excellent customer service. Lead the Planning and Setup, Monitoring, and Closeout phases of study management which includes...
assigned program. Involved in study related activities from the protocol design stage onwards, providing input into the study...The CDM will perform scientific (complex) clinical data review in close collaboration with the Study Responsible...
conduct of the clinical study data review and capture Verifies site compliance with electronic data capture requirements May... and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture – where you can...
and reproducible coding of clinical study data, adhering to established J&J R&D guidelines and coding processes. You'll contribute...: Lead medical coding activities for lower-to-moderate size therapeutic areas, ensuring compliance with Regulatory Authority...
, Contracts, Clinical Coordination and Clinical Operations Reviews program or study specifics to define project scope, timelines... issues Trial Start Up Group Sets the vision, the strategic planning, execution, and oversight of study start-up...
and reproducible coding of clinical study data, adhering to established J&J R&D guidelines and coding processes. You'll contribute...: Lead medical coding activities for lower-to-moderate size therapeutic areas, ensuring compliance with Regulatory Authority...
further! In this role, you will ensure accurate, consistent and reproducible coding of clinical study data, adhering... therapeutic areas, ensuring compliance with Regulatory Authority and Industry standards for coding practices and processes. Drive...
Programming (e.g. GCP, study procedures) Proven communications and negotiation skills, ability to work well with others globally.... Complies with project / study standards and specifications following internal and regulatory guidelines. Oversees programming...
conduct of the clinical study data review and capture Verifies site compliance with electronic data capture requirements May... and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture – where you can...