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Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- 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.
Requirements
What you’ll need- **About You**
- If you are a results-driven Senior Project Manager with a proven track record of leading complex clinical trials from start-up to closeout. If you thrive in fast-paced environments, excel at aligning teams and stakeholders, and take pride in delivering projects on time, on budget, and with uncompromising quality then this role is for you.
- **To be successful, we are looking for the following traits and behaviors: **
- - 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 & Infectious Diseases programs, including oversight of specialized vendors, timelines, safety considerations, and global study execution. Cell & Gene therapy is a plus.
- - 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).
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 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
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
project managementclinical trial managementregulatory complianceGCPSOPsrisk mitigationbudget controldata privacy practicesclinical trial delivery lifecycleOncology
Soft Skills
leadershipstakeholder alignmentcommunicationanalytical skillsfinancial acumenproblem-solvingteam collaborationorganizational skillsresults-drivenadaptability
