Project Data Manager

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October 31

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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 be limited to:** • - Serve as the primary data management contact for internal teams, sponsors, and external vendors. • - Lead and coordinate Biometrics/DM project teams to deliver studies on scope, timeline, and budget. • - Develop and execute project plans, including training plans, risk management, and communication pathways. • - Oversee vendor selection, qualification, and ongoing management to ensure quality delivery. • - Ensure consistency and quality across studies, including DMP, CRF design, data cleaning, and statistical deliverables. • - Manage project finances, monitor scope, drive contract amendments when needed, and maintain audit-ready documentation.

🎯 Requirements

• **About You** • If you’re a seasoned Clinical Data Management expert with deep experience leading studies from start-up through database lock across multiple phases and therapeutic areas. You thrive in combining technical mastery; CDISC standards, complex databases, and global regulatory frameworks with exceptional communication and client-facing skills that build trust and drive results. If you thrive in fast-paced environments, love solving complex challenges, and take pride in delivering data that fuels clinical breakthroughs, this role is built for you. • **To be successful we are looking for the following traits and behaviors: ** • - At least 8 years leading DM activities across multiple clinical trial phases (I–IV) and therapeutic areas, including database design, cleaning, and lock. • - Strong knowledge of ICH-GCP, 21 CFR Part 11, GDPR/HIPAA, CDISC standards, and relational database principles to ensure compliant, high-quality data management. • - Proven ability to manage cross-functional teams, vendors, budgets, and timelines, while coordinating complex, multi-study projects and client communications. • - Exceptional problem-solving, attention to detail, and ability to translate complex technical or regulatory requirements into clear, actionable recommendations for stakeholders.

🏖️ 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