Director - Clinical Development

July 25

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Adverum Biotechnologies

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We are on a global mission to establish gene therapy as a new standard of care for highly prevalent ocular diseases.

Gene Therapy • Biotechnology • Rare Diseases • Ophthalmology • Retina

51 - 200

💰 $217M Post-IPO Equity on 2020-08

Description

• Provide scientific and technical expertise for assigned clinical programs • Set strategy across the clinical development program, oversight of strategic study design, study start up, CRO and vendor management, clinical data and safety monitoring, analysis and reporting of studies • Contribute as team leader and author in protocol development, clinical study reports, investigator brochures, periodic safety update reports, international regulatory submissions, interactions with US and Global Health Authorities • Writes and/or reviews abstracts, posters, content for scientific meetings, conferences, other events and presentations, contributes to scientific publication of study results • Serves as CD liaison/point-of-contact for inquiries from clinical operations, clinical research organizations (CROs), etc., collaborates with others in the review of safety narratives and other safety-related guidelines and documentation • Represents CD in sub-teams and addresses CD study or other program-specific questions, develops and provides input for clinical presentation slides and other materials for meetings and ongoing communication • Collaborates with a variety of internal and external partners and stakeholders, such as clinical investigators, clinicians, health authorities, scientists and KOLs, as well as internal groups, including regulatory research, operations, legal and business development • Participates in ongoing enhancements and development of team processes, structures, and tools • Develops and mentors study team members

Requirements

• MD, PhD or OD required; PharmD with relevant experience may be considered • 5-10 years of clinical research and/or clinical development experience within the pharmaceutical or biotech industry, CRO health-related consulting company, or biomedical/clinical experience within academia (or a combination of fore mentioned.) Gene therapy and/or ophthalmology (retina) experience preferred. • Ability to proactively predict issues and solve problems • Ability to drive decision-making within a multi-disciplinary, multi-regional, matrix team • Diplomacy and positive influencing abilities • Committed to developing and mentoring team • Therapeutic area knowledge relevant to mechanism of action and retinal drug development • Understanding of US and Global Regulatory requirements