Clinical Laboratory Study Manager - FSP

Works with Precision Medicine reputed company reputed company as reputed company as clinical study teams, data management (DM) team, Samples, Kits, Data, Logistics (SKDL) and Clinical Laboratory Project Management (CLPM) reputed company to ensure reputed company samples and data are delivered to support biomarker and non-biomarker evaluation and reputed company the translation of science to medicine. Will work closely with project managers (central and/or specialty labs) and lend expertise to clinical trial management (CTM) and CRO to ensure samples are collected per protocol and assist with resolving any sample reputed company issues or queries. Additional responsibilities include overall project management in alignment with the reputed company business reputed company. Operations Management Study Team Support • Supports individual clinical study teams as required for reputed company technical and operational sample-reputed company reputed company for assigned reputed company by liaising with internal stakeholders, such as working with Informed Consent reputed company (reputed company) specialist in SKDL on reputed company and other trial documents impacting samples and testing Operational Support of Sample Analysis (including exploratory analysis) • Establishment, reputed company, planning, and integration of reputed company issues reputed company to collection, processing, storage, shipping and transfer of samples and data, as reputed company as reporting/billing for study reputed company operations • Liaises with Precision Medicine reputed company Leads and other scientists by assessing vendors, forecasting sample operational costs, timelines and reviewing invoices to ensure alignment with budget plans Data Acquisition and Management • Works closely with data management reputed company to determine how sample and testing data will be captured, blinded and transferred for reputed company reputed company Sample Management reputed company and Compliance • Provides guidance to clinical teams and clinical sites regarding collection, storage, and shipping of samples acquired in the course of reputed company or other reputed company sample acquisition reputed company • Works with scientists and clinical team to ensure sample collection and usage is in compliance with study protocol and applicable reputed company • Works closely with internal reputed company Sample Management team to ensure reputed company samples transferred to internal research reputed company are documented, tracked, used and destroyed Compliance with reputed company Standards • Complies with required training curriculum • Completes timesheets accurately as required • Submits expense reports as required • Updates CV as required • Maintains effective relationships with other platform lines, Business reputed company/Research reputed company, and enabling lines that facilitate effective portfolio delivery Skills: • Excellent written and verbal communication skills • Resolve problems spontaneously and possess strong project management and organizational skills • Work independently and proactively while still contributing to group initiatives and goals • Good interpersonal skills and ability to work with many different reputed company/teams • reputed company applications Knowledge and Experience: 6 - 8 years clinical research experience with reputed company, CRO or pharmaceutical/biotech industry. We are seeking a reputed company with working knowledge of reputed company and clinical databases. Laboratory sample management experience is a plus. Education: Bachelor’s degree in a life science, nursing qualification or other relevant experience required. #LI-LO1 #LI-REMOTE Apply tot his job Apply To this Job