Project Manager II – Oncology

🔥 2 minutes ago

🇺🇸 United States – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👷‍♀️ Project Manager

👻 Ghost score 10%

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Allucent

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

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.

📋 Description

• Lead cross-functional teams to deliver clinical trials on time, within scope, and on budget • Develop and execute project plans aligned with GCP, SOPs, and regulatory standards • Serve as the primary point of contact for sponsors, vendors, and internal teams • Select, manage, and oversee vendors • Proactively address challenges, scope changes, risks, and resource allocation • Lead key meetings and ensure the Trial Master File and study records are complete and inspection-ready • Drive global clinical trials from study start-up through final delivery

🎯 Requirements

• Minimum Bachelor’s degree in life science, healthcare and/or business degree • Minimum 6 years of relevant work experience, specifically experience in drug development and/or clinical research • Minimum 1 year of project management experience, specifically as a clinical project manager • Strong expertise managing the unique operational complexities associated with Oncology 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)

🏖️ 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