Senior Clinical Project Manager

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November 12

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Allucent

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Biotechnology • Pharmaceuticals • Science

Allucent is a leading partner for small and mid-sized biotech companies, offering innovative regulatory and clinical development solutions. With over 30 years of experience, Allucent specializes in therapeutic expertise, clinical pharmacology, regulatory strategy, drug safety, and the pharmacovigilance processes needed to bring new therapies to market. Their comprehensive services address challenges from early-phase drug discovery through clinical trials and post-marketing surveillance, supporting various therapeutic areas such as oncology, infectious disease, neurology, autoimmune diseases, and rare diseases. Allucent's commitment to fostering breakthrough science helps biotech companies navigate the complexities of drug development efficiently and effectively.

1001 - 5000 employees

🧬 Biotechnology

💊 Pharmaceuticals

🔬 Science

📋 Description

• **Your main responsibilities will include but not limited to: ** • - 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

• **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 5 years of experience in drug development and/or clinical research, with at least 2-3 years of clinical trial project management experience • - Minimum Bachelor’s degree in life science, healthcare and/or business degree • - 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

• **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