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Allucent

Global drug development services for biotech

Project Director - Oncology

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeRemote in USANo salary listed

About the Job

Requirements

  • A minimum bachelor's degree in life science, healthcare, and/or business is required; a master's degree or greater is preferred.
  • A minimum of 8 years of relevant work experience in drug development and/or clinical research is required.
  • A minimum of 8 years of project management experience as a clinical project manager is required, including experience managing global clinical trials.
  • At least 5 years of clinical project management experience is required.
  • Extensive clinical project management experience is required.
  • Expert knowledge of ICH-GCP (R3), data and patient privacy practices, and applicable local regulatory requirements is required.
  • Therapeutic expertise in Oncology is required.
  • An equivalency consisting of a combination of appropriate education, training, and/or directly related experience may be considered to meet the requirements.

Responsibilities

  • Oversee clinical trial projects and programs, ensuring overall quality and management of delivery.
  • Oversee budgets, review and approve proposal content and costing, solve problems with project teams, and balance competing priorities.
  • Serve as the key client contact for delivery of scope, customer satisfaction with services and capabilities, and assessment of client needs.
  • Lead the project team and support recruitment and interviewing of new employees.
  • Control and monitor the quality and full-service delivery of clinical trial projects for customers.
  • Drive continuous improvement of processes within Global Clinical Operations.

Desired Qualifications

  • CRA experience is preferred.
  • A master's degree or greater is preferred.

About the Company

Allucent

Global drug development services for biotech

Allucent provides global drug development services aimed at small and mid-sized biotech firms. Its offerings include therapeutic strategies, clinical trial operations, biometrics, and clinical pharmacology to support regulatory planning and execution. The company works by partnering with biotech teams to design and run clinical studies, extend in-house capabilities, and ensure accurate data collection and analysis across more than 60 countries. It differentiates itself by focusing on smaller biotech clients with end-to-end, globally coordinated development programs, backed by deep regulatory and scientific expertise and long-term collaborations. The goal is to help clients bring new therapies to market safely and efficiently through practical, hands-on development support.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Cary, NC
Founded
2022

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