Project Director, Global Project Leadership

Posted 2 Days Ago
Be an Early Applicant
Hiring Remotely in United States
Remote or Hybrid
Senior level
Healthtech • Biotech • Pharmaceutical
The Role
Oversee global clinical trial projects from planning through completion, managing scope, budgets, resources, risks, quality, regulatory compliance, and client relationships. Lead cross-functional teams, resolve issues, approve proposals, forecast finances, support recruitment, and supervise project staff. The role requires expertise in clinical trial delivery, drug development, ICH-GCP, global regulations, and data-driven project solutions. Approximately 10% international and domestic business travel is required.
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 (hybrid*/remote). As a Project Director at Allucent, you are responsible for overseeing and managing all aspects of the clinical study trials for Neuroscience or Immunology and Infectious Diseases. Experience in Cell and Gene Therapy is a plus. This role plays a pivotal part in ensuring the successful execution of trials, from initial planning through to completion, with a focus on safety, regulatory compliance, and efficient project management.

In this role your key tasks will include:

Project oversight:

  • Responsible for overall quality and management of the delivery clinical trial projects and programs
  • Manages complex, cross-functional resource requirements in line with budgeted, time, scope, and quality expectations for project delivery
  • Oversees budgets and ensuring correct financial forecasting, planning, invoicing and timely implementation of out of scope activities
  • Reviews and approves content and costing of proposals
  • Ensures effective risk management across the project delivery lifecycle
  • Negotiates and influences internal and external team members in a professional manner and with successful outcomes
  • Effectively solves problems with projects teams by applying strategic thinking and conflict resolution skills
  • Balances multiple competing priorities, with effective and efficient resource utilization across projects and programs

Client management:

  • Serves as key contact for assigned clients on delivery of scope, customer satisfaction on services and capabilities and the assessment of client needs

Leadership:

  • Shows knowledge of and insight into general business principles and practices, and is able to balance business priorities
  • Demonstrates a growth mindset, and approaches complex challenges with creativity and flexibility
  • Leads by example and encourages team members to develop strong solutions for clinical trial delivery
  • Supports the recruitment and interviewing of new employees
  • Responsible for supervision of project staff and communication with functional managers, including performance feedback
  • 10% of Business travel is required for this position, including possible international travel

Requirements

To be successful you will possess:

  • Minimum Bachelor’s degree in life science, healthcare and/or business degree; Master’s degree or greater preferred
  • Minimum 7 years of relevant work experience
  • Minimum 7 years of experience in drug development and/or clinical research
  • Extensive clinical project management experience, with at least 5 years of clinical project management experience
  • Preference for candidates with CRA experience
  • Expert knowledge of ICH-GCP(R2), data and patient privacy practices, and applicable (local) regulatory requirements
  • Strong financial acumen, administrative excellence and analytical skills
  • Experience managing global clinical trials
  • Excellent written and verbal communication, planning, critical thinking and organizational skills, including command of English language
  • Proficiency with various applications including but not limited to Microsoft Word, Excel, and PowerPoint required
  • Clinical trial delivery process expertise
  • Strong general administrative skills and experience
  • Outgoing and client focused
  • Proactive and solution oriented
  • Strong presentation and networking capabilities
  • Experience applying a data driven approach to drive clinical trial delivery solutions

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
  • Access to online soft-skills and technical training via GoodHabitz and internal platforms

Disclaimers:

*Our hybrid work policy encourages a dynamic work environment, prescribing 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-DH-1 #LI-Remote #LI-Hybrid

Skills Required

  • Bachelor's degree in life sciences, healthcare, and/or business
  • Master's degree or higher
  • At least 7 years of relevant work experience
  • At least 7 years of experience in drug development and/or clinical research
  • At least 5 years of clinical project management experience
  • Experience managing global clinical trials
  • Expert knowledge of ICH-GCP(R2)
  • Knowledge of data and patient privacy practices
  • Knowledge of applicable local regulatory requirements
  • Strong financial acumen, administrative excellence, and analytical skills
  • Excellent written and verbal English communication skills
  • Strong planning, critical thinking, organizational, presentation, and networking skills
  • Proficiency with Microsoft Word, Excel, and PowerPoint
  • Clinical trial delivery process expertise
  • Strong general administrative skills and experience
  • Client-focused, proactive, and solution-oriented approach
  • Experience applying a data-driven approach to clinical trial delivery solutions
  • Clinical research associate experience
  • Experience in cell and gene therapy
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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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