United StatesSupport customers remotely with communications, patient orders, laboratory testing inquiries, and issue resolution at ARUP Laboratories, a clinical and anatomic pathology reference laboratory.
Contract Senior Clinical Research Associate overseeing clinical trial sites for Lotus Clinical Research. The role covers GCP compliance, essential documentation, investigational product accountability, and study close-out.
Contract Senior Clinical Research Associate responsible for monitoring clinical-trial sites and supporting study execution. Ensures compliance with GCP, FDA, ICH, protocol, and study-document requirements through site visits.
Abbott is hiring a senior analyst to manage customer rebate and fee programs for its medical device business in Austin. The role covers contract analysis, payment calculations, performance tracking, and coordination with sales, finance, accounting, legal, and hospital customers.
Lead AstraZeneca’s regional cell therapy patient operations across the Northeast. Oversee territory teams, site activation, operational strategy, and cross-functional execution.
Lead verification of Albus Health’s hardware, software and cloud systems, building the evidence required for regulated medical-device development. Support FDA 510(k) readiness for its contactless clinical-trial health platform.
Lead clinical operations for Borealis Biosciences’ RNA therapeutics programs in kidney disease, including upcoming Phase 1/2 trials. Build teams, oversee CROs and vendors, and establish the infrastructure needed for successful clinical execution.
United States
Massachusetts
PennsylvaniaLead strategic clinical site engagement for CSL Behring, a global biotherapeutics company. Shape feasibility, recruitment, retention, trial delivery, and the site experience across clinical programs.
United StatesMassachusettsPennsylvaniaLead scientific content strategy for Madrigal’s MASH therapeutics, supporting compliant omnichannel communications, medical congresses, and collaboration across medical affairs.
United States
New JerseyPennsylvaniaLead global scientific and value content strategy for payor medical affairs at MSD. Oversee scientific planning, payer-focused content, cross-functional programs, analysis, and team development.
Natera seeks a Regulatory Affairs Advisor to advance FDA Pharma, IVDR, and IVD strategies for its clinical genetic testing business. The role covers submissions, product registrations, regulatory guidance, and cross-functional program leadership.
United StatesNew JerseyPennsylvaniaLead digital and AI innovation across Regulatory CMC for MSD medicines, vaccines, and animal health products. Connect research, manufacturing, and regulatory operations through automation, modern authoring, and integrated technology solutions.
United StatesNew JerseyLead and oversee late-phase endocrine clinical trials at Ascendis Pharma in a hybrid Princeton role. Analyze clinical data, support regulatory submissions, and advance therapies addressing unmet medical needs.
Senior Clinical Research Associate II overseeing UK clinical trial sites for CTI Clinical Trial and Consulting Services. The role includes site visits, remote monitoring, enrollment support, and regulatory compliance.
Coordinate operational planning, resource management and reporting for Carnall Farrar’s healthcare consultancy. The role focuses on CMap administration, data quality, associate coordination and resourcing support.
Lead regional oncology clinical trial delivery for BeOne Medicines, coordinating operations, vendors, timelines, budgets, quality, and regulatory execution across assigned countries.
Lead regional oncology clinical trial delivery for BeOne Medicines across timelines, sites, vendors, budgets, compliance, and operational teams. Oversee study execution from feasibility through closeout while maintaining quality and inspection readiness.
Lead scientific contributions to CSL’s hematology clinical development programs. Support study execution, clinical data interpretation, regulatory documentation, medical monitoring, and external oversight committees.
United StatesMassachusetts
New YorkPennsylvaniaDrive inside sales for Element Biosciences’ genomics instruments, sequencing consumables, and services across the Northeast. Manage qualified leads, Salesforce pipeline activity, customer presentations, and account growth.
Sell Clarius AI-powered mobile ultrasound products to healthcare professionals across Canada. Manage inbound leads, outbound prospecting, and early-stage sales pipelines.
