Senior Scientific Project Manager

Responsibilities: Provide project management oversight for biopharmaceutical clients, managing analytical testing, method development, and validation under GLP. Lead vendor contracting, coordinate study documents, and ensure accurate data transfer and sample logistics.

Requirements: Requires a Bachelor's or Master's in Life Sciences with 5-6 years of experience in drug development for the Senior level. Must have extensive knowledge of bioanalysis in regulatory environments and proficiency in MS Project and Smartsheet.

Key skills: Vendor Management, Project Management, Bioanalysis, GLP/GCP Compliance, Method Development, Method Validation, Budgeting and Forecasting, Sample Logistics, Data Review, Technical Transfer, Oncology, MS Project, Smartsheet, SharePoint, Change Management, Clinical Trial Coordination

Keywords: GLP, GCP, Immunoassays, Bioassays, Pharmacokinetic, Flow Cytometry, PK/ADA, Biomarker Analysis, Oncology, PMP, SOW, eCRF, ICF, MS Office Suite, MS Project, Smartsheet, SharePoint, Clinical Research Organizations, CRO, Functional Service Provider, FSP, Bioanalytical Processes, Drug Development, Clinical Trials