Project Director

Allucent

Project Director responsible for managing clinical trials and project teams in biopharmaceuticals at Allucent. Ensuring customer satisfaction and regulatory compliance in clinical operations.

Posted 5/18/2026full-timeRemote • 🇺🇸 United StatesLeadWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

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

What you’ll need

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

Benefits

Comp & perks

**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

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

project managementclinical project managementdrug developmentclinical researchbudget managementproposal reviewICH-GCPdata privacy practicesregulatory complianceanalytical skills

Soft Skills

customer satisfactionproblem solvingleadershipcommunicationgrowth mindsetteam managementadministrative excellenceinterpersonal skillsrecruitmentorganizational skills