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CMC Submission Lead
CMC Submission Lead | 12-Month Contract | Fully Remote (Europe)We are supporting a global pharmaceutical and biotechnology organisation seeking an experienced CMC Submission Lead to support high-profile regulatory submissions across both development-stage and commercial products.This role will be responsible for leading and coordinating CMC submiss...
CRA West Coast USA
Contract CRA / Senior CRA - West Coast, USAContract: 12 months Start Date: December 2026 Location: US West Coast Employment: W2 Contract Therapeutic Area: Respiratory / Asthma and/or Dermatology Study Phases: Phase II & Phase IIIRole OverviewWe are supporting a client seeking an experienced Clinical Research Associate (CRA) / Senior Clinical Resear...
Medical Writer
We are seeking an experienced Medical Writer with a strong background in Health Economics & Outcomes Research (HEOR), Health Policy, and Market Access communications to support the development of high-quality scientific and technical deliverables. The successful candidate will have experience working within the pharmaceutical, biotechnology, or hea...
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Hematology Account Manager Washington/Alaska | CONTRACT
Hematology Account Manager - Washington & Alaska (Contract)Contract Duration: 6-12 Months Compensation: $90-$110/hour + bonus Additional Compensation: Monthly car allowance providedPosition OverviewThe Hematology Account Manager will be responsible for building relationships with hematologists, oncologists, and key accounts to educate them on the p...
External Quality Senior Specialist
Our client is seeking an experienced External Quality Senior Specialist to support Quality Process & Operations activities within a global pharmaceutical environment. This role focuses on strengthening External Quality processes, supplier oversight, quality systems management, regulatory compliance, and continuous improvement initiatives across ex...
QMS Consultant
OverviewWe are seeking an experienced Quality Systems Manager to lead and continuously improve the Quality Management System (QMS) within a GMP-regulated pharmaceutical environment. This role will be responsible for ensuring compliance with global regulatory requirements while driving quality excellence across manufacturing, laboratory, supply chai...