Adverum Biotechnologies, Inc. is a mission-driven clinical-stage company that aims to establish gene therapy as a new standard of care for highly prevalent ocular diseases with the aspiration of developing functional cures to restore vision and prevent blindness. Leveraging the research capabilities of its proprietary intravitreal (IVT) platform, Adverum is developing durable, single-administration therapies designed to be delivered in physicians’ offices to eliminate the need for frequent ocular injections to treat these diseases. By overcoming the challenges associated with current treatment paradigms for these debilitating ocular diseases, Adverum aspires to transform the standard of care, preserve vision, and create a profound societal impact around the globe.
Note to Recruiters and AgenciesAll recruiter and agency inquiries must go through Adverum’s internal Talent Acquisition team.  Unsolicited resumes sent to Adverum will be considered property of Adverum.   Adverum’s Talent Acquisition team must expressly engage agencies for any requisition.  Direct contact with hiring managers by agencies will not be tolerated and may affect your ability to work with Adverum in the future.
Adverum is looking for a SOM (Contract - Sponsor Oversite Manager).  The SOM (contract) is a critical position within the clinical team at Adverum. In close collaboration with the Clinical Trial Manager and/or Study Director, the SOM will work to manage and provide daily operational oversight of the Contract Research Organization (CRO), study vendors, and clinical trial sites. The SOM will partner with the Medical Monitor and other internal and external constituents to ensure clinical trial activities and deliverables are completed on time and in accordance with regulatory requirements, Good Clinical Practice (GCP) guidelines, and company SOPs.What you'll do:Independently manages the study start-up activities for multi-center, US, and/or global-based studiesMay perform on-site sponsor oversite visits (feasibility, SIV, IMV, Close-out) or with CRO CRAs as needed to assess the sites’ and CRA’s overall performanceProvides monitoring oversight by reviewing monitoring schedules, metrics, and reportsResponsible for clinical site training and site adherence to protocol, all applicable GCP/ICH guidelines, regulations, statutes and SOPsLeads or participates in vendor management activitiesPerforms in-house routine data listing reviewAssists in managing and/or leading the day-to-day operations of assigned studies to ensure completion per established project team goals and objectives in compliance with applicable GCP/ICH guidelines and other regulatory requirementsSupports CTM and/or Study Director and cross-functional representatives as required in relationship management tasks (e.g. contracts, study logistics, patient enrollments, safety, data management, etc.) to accurately coordinate clinical study activitiesMentors and coaches junior staff new to Clinical Research (e.g. Clinical Trial Assistant)Assists with the development of protocol, informed consent development, CRFs, tracking forms, and other study-related documentsPerforms other duties and assignments as required for the overall success of the projects. Duties my change based on the status of clinical programs and ongoing needs of the organizationOther responsibilities may be assigned as neededAbout you: Working knowledge of ICH/GCP and FDA guidelinesEffective verbal and written communication skillsAttention to detail and organizational skillsAbility to “roll up your sleeves” and individually contribute results to a research and development effortOphthalmology experience preferred but not requiredProficiency in MS Word, Excel, and PowerPointAbility to travel up to 20%BS/BA, RN, or equivalent with at least 4 years of clinical trial monitoring/ clinical trial management and vendor management experience$50 - $60 an hourThis is a contract role, starting at 6 months. Hourly rate will depend on experience and location.
The hourly range for this position is $ to $60.00/hr USD. This hourly range is an estimate, and the actual range may vary based on a candidate’s qualifications, including education, length of experience, location, and market data.  At Adverum, Inclusion and Diversity are at our core. We believe in the power of being your authentic self.  We strive to create the space which allows for everyone in our Adverum Community to not only feel safe but encouraged to speak, learn from each other, grow in their professions and be the very best versions of themselves no matter what their age, ethnic background, gender, origin, religion or sexual orientation.