Adverum Biotechnologies is hiring a
Clinical Science Liaison

Summary

The Clinical Science Liaison will collaborate with various teams to manage clinical trials, review protocols, maintain site subject trackers, support training activities, and more. The ideal candidate should have a life science degree and at least 5-7 years of experience, strong interpersonal skills, and the ability to work cross-functionally.

Requirements

• MD, PharmD, or PhD in life science field
• At least 5-7 years of therapeutic area experience/ research or substantial patient care experience
• Strong interpersonal, presentation, and communication skills
• Ability to work collaboratively and cross-functionally
• Ability to appropriately apply knowledge of GCP and applicable regulations and guidance
• Ability to coordinate with study sites and manage clinical and medical science responsibilities when traveling

Responsibilities

• Establish working relationships with clinical coordinators, site staff, PIs/SubIs, and KOLs
• Act as the interface between the Adverum team and external stakeholders including vendors, clinical sites, and CROs
• Perform activities including study startup, clinical trial conduct, and pre-launch
• Review protocols, informed consent forms, and other documents relating to the clinical trial
• Maintain and update site subject trackers
• Support US and Ex-US site training activities, including presenting at SIV, Site training, IM, KOL, and Study Coordinator forums
• Assist in advisory board planning and other external-facing events
• Attend medical conferences as the clinical operations representative and/or medical affairs representative to meet with investigators and assist with conference strategy
• Establish regular lines of communication and conduct site engagement visits with study investigators and site staff
• Lead alongside clinical operations and clinical development to implement effective local and regional subject recruitment strategies focusing on diversity
• Identify and mitigate challenges related to clinical trial protocols
• Comply with internal and external SOPs and support the development of internal processes and procedures as needed
• Communicate key clinical research issues and insights from industry leaders to appropriate departments to help shape program development

Benefits

• Salary range: $155,000 - $170,000 per year
• Opportunity to earn an annual bonus
• 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