Sr. Clinical Project Manager (United States)
About The Position
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. Looking to take your project management expertise to the next level? Join us as a Senior Project Manager (Sr. PM) and lead the delivery of complex clinical trials that make a meaningful impact for patients worldwide. We are seeking a strategic and execution-focused leader with strong experience managing Oncology, Neurology, and Immunology & Inflammation therapy studies who thrives in a fast-paced, collaborative environment. As a Senior Project Manager, you will lead with impact and drive global clinical trials from study start-up through final delivery. You’ll oversee cross-functional teams, ensuring studies remain on track, on budget, and compliant with GCP and regulatory requirements while serving as the primary point of contact for sponsors, vendors, and internal stakeholders. With a focus on proactive problem-solving, risk mitigation, and operational excellence, you’ll play a critical role in delivering high-quality clinical programs that exceed client expectations.
Requirements
- Minimum Bachelor’s degree in life science, healthcare and/or business degree
- Minimum 5 years of experience in drug development and/or clinical research, with at least 2-3 years of clinical trial project management experience
- Strong expertise managing the unique operational complexities associated with Oncology, Neurology, and Immunology & Inflammation programs, including oversight of specialized vendors, timelines, safety considerations, and global study execution.
- Expert knowledge of ICH-GCP(R2), data and patient privacy practices, and applicable (local) regulatory requirements
- Demonstrates strong financial acumen, administrative excellence and analytical skills
- Experience managing all phases of the full-service clinical trial delivery lifecycle (Start-up, Maintenance, Close-out).
Nice To Haves
- Cell & Gene therapy is a plus.
Responsibilities
- Driving project success by leading cross-functional teams to deliver clinical trials on time, within scope, and on budget.
- Ensuring excellence and compliance by developing and executing project plans aligned with GCP, SOPs, and regulatory standards.
- Aligning stakeholders by serving as the primary point of contact for sponsors, vendors, and internal teams.
- Optimizing vendor performance through strategic selection, management, and oversight.
- Mitigating risks and control budgets by proactively addressing challenges, scope changes, and resource allocation.
- Maintaining inspection-ready documentation by leading key meetings and ensuring the Trial Master File and study records are complete.
Benefits
- 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 enriching 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 internal platforms
- Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects
- Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees
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What This Job Offers
Job Type
Full-time
Career Level
Senior
