Project Director (Oncology)

Reposted 6 Days Ago
Be an Early Applicant
Hiring Remotely in United States
Remote
Senior level
Healthtech • Biotech • Pharmaceutical
The Role
Lead and oversee global oncology clinical trial projects, manage budgets and proposals, ensure quality and compliance (ICH-GCP, privacy, local regs), serve as primary client contact, lead project teams, drive customer satisfaction and continuous process improvement.
Summary Generated by Built In

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.

We are looking for a Project Director (PD) to join our A-team (office-based*/remote). As a PD at Allucent, you are responsible for coordinates and oversees operational project teams, customer satisfaction and continuous improvement of processes within the Global Clinical Operations (GCO) department. This position controls and monitors the quality and full-service delivery of clinical trial Allucent customers.

About this role:

As a proactive project director, you will:

  • Oversee the project and be responsible for the overall quality and management of the deliver clinical trial projects and programs. This includes overseeing the budget, reviewing and approving content and costing of proposals, problem solving with project teams, and balancing multiple competing priotities.
  • Serve as the key contact for assigned clients on delivery of scope, customer satisfaction on services and capabilities and the assessment of client needs.
  • Lead the project team. You will demonstrate knowledge of and insight into general business principles and practices, demonstrate a growth mindset, and support the recruitment and interviewing of new employees.

Requirements

To be successful, you will posess:

    • Minimum Bachelor’s degree in life science, healthcare and/or business degree; Master’s degree or greater preferred  
    • Minimum 8 years of relevant work experience, specifically experience in drug development and/or clinical research  ; CRA experience preferred.
    • Minimum 8 years of project management experience, specifically as a clinical project manager ; managing global clinical trials required
    • Extensive clinical project management experience, with at least 5 years of clinical project management experience  
    • Expert knowledge of ICH-GCP(R3), data and patient privacy practices, and applicable (local) regulatory requirements  
    • Strong financial acumen, administrative excellence and analytical skills   
    • In some cases, an equivalency—consisting of a combination of appropriate education, training, and/or directly related experience—will be considered appropriate for an individual to meet the requirements of this role  
    • Therapeutic expertise in Oncology required

Benefits

Benefits of working at Allucent include:

  • Comprehensive benefits package per location
  • Competitive salaries per location
  • Departmental Study/Training Budget for furthering professional development
  • Flexible Working hours (within reason)
  • Opportunity for remote/hybrid* working depending on location
  • Leadership and mentoring opportunities
  • Participation in our Buddy Program as a new or existing employee
  • Internal growth opportunities and career progression
  • Financially rewarding internal employee referral program

Disclaimers:

*Our office-based work policy encourages a dynamic work environment, prescribing a minimum of 2 days in office per week for employees within reasonable distance from one of our global offices.

“The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”

#LI-Remote #LI-Hybrid #LI-TCW

Skills Required

  • Bachelor's degree in life science, healthcare, or business
  • Master's degree or greater
  • Minimum 8 years relevant experience in drug development and/or clinical research
  • CRA (Clinical Research Associate) experience
  • Minimum 8 years project management experience, specifically as a clinical project manager; managing global clinical trials
  • At least 5 years of extensive clinical project management experience
  • Expert knowledge of ICH-GCP(R3), data and patient privacy practices, and applicable local regulatory requirements
  • Strong financial acumen, administrative excellence, and analytical skills
  • Therapeutic expertise in Oncology
  • Equivalency of education, training, and/or directly related experience may be considered
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The Company
HQ: Cary, NC
1,436 Employees

What We Do

Allucent is on a mission to help bring new therapies to light by solving the distinct challenges of small and mid-sized biotech companies. The company is purpose-built through the convergence of leading providers to address this unmet need. Today, Allucent is a global provider of comprehensive drug development solutions, including consulting, clinical operations, biometrics and clinical pharmacology across a variety of therapeutic areas. With more than 30 years of experience in over 60 countries, Allucent’s individualized partnership approach provides experience-driven insights and expertise to assist its clients in successfully navigating the complexities of delivering novel treatments to patients.

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