Director - Senior, Clinical Program Management

March 1

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Logo of Adverum Biotechnologies

Adverum Biotechnologies

Adverum Biotechnologies is a company focused on developing gene therapies to treat debilitating ocular diseases. Their mission is to establish gene therapy as a new standard of care, particularly in treating conditions like wet age-related macular degeneration (wet AMD), which is a leading cause of blindness globally. The company is advancing their investigational gene therapy Ixo-vec, designed to provide a long-lasting treatment through a single in-office administration, which could replace the current standard of frequent and painful eye injections. By leveraging their proprietary adeno-associated virus (AAV) vector platform, Adverum aims to transform the standard of care, improve accessibility to treatment, and achieve significant societal impact by restoring vision and preventing blindness.

Gene Therapy • Biotechnology • Rare Diseases • Ophthalmology • Retina

51 - 200 employees

Founded 2013

🧬 Biotechnology

💊 Pharmaceuticals

💰 $217M Post-IPO Equity on 2020-08

📋 Description

• Adverum Biotechnologies, Inc. aims to establish gene therapy as a new standard of care for ocular diseases. • This role oversees and drives the strategic planning, execution, and delivery of clinical programs. • Collaborates with cross-functional teams to ensure clinical trials are conducted on time and within budget. • The ideal candidate will have a robust background in clinical trial management, strong program and project management skills, and a strategic mindset.

🎯 Requirements

• Bachelor’s degree in life sciences, healthcare, or a related field required. Advanced degree (MS, PharmD, or PhD) preferred. • Minimum of 10-12+ years of experience in clinical program management or clinical trial operations within the biotech, pharmaceutical, or CRO industry. • Proven experience managing complex, multi-center clinical programs from initiation to close-out. • Proficiency with project management tools and software, such as MS Project, GAANT charts or equivalent. • Strong understanding of clinical trial regulations (FDA, EMA, ICH-GCP) and regulatory requirements. • Ability to analyze and interpret clinical data and program metrics to inform strategic decisions.

🏖️ Benefits

• Employees are eligible to participate in the applicable Company equity incentive award plan. • Employees are eligible to participate in the Company’s standard employee benefit programs, which currently include: medical, dental, vision, 401k, STD/LTD, life and accident insurance, and either paid time off or flexible paid time off.

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