Avalo Therapeutics

Avalo Therapeutics

Clinical Trial Manager

Chesterbrook, PA

Sponsorship not specifiedDetected 13 days ago
GCPNegotiationForecastingVendor ManagementHRClinical TrialsClinical ResearchResearchCommunicationProblem SolvingTime ManagementMicrosoft Office

About the role

  • Reporting to the Executive Director of Clinical Development Operations (or delegate), the Clinical Trial Manager (CTM) plays a key role in the planning, execution, and delivery of clinical trials.
  • Identify, communicate, and help resolve study-related risks and issues in a timely and thoughtful manner
  • Review vendor invoices and help monitor for trends or scope changes

Responsibilities

  • Support and/or lead key aspects of clinical trial operations, including vendor management, site start-up, and monitoring activities
  • Contribute to the development, review, and maintenance of study documents (e.g., protocols, amendments, informed consent forms, monitoring plans, study manuals, eCRFs, IVRS/IWR systems)
  • Foster clear, respectful, and proactive communication between internal teams and external partners, ensuring alignment on study goals and expectations
  • Support the development, management, and negotiation of clinical site budgets
  • Track and support site activation progress, partnering with CROs and internal stakeholders to address barriers and improve timelines
  • Support site identification, feasibility assessments, and site selection processes
  • Build and maintain strong, respectful relationships with vendors, CROs, and clinical sites
  • Support planning and execution of Investigator Meetings and training activities
  • Assist with clinical supplies planning, including forecasting and accountability support

Requirements

  • Approximately 5+ years of experience in clinical research or clinical operations within biotech, biopharma, or related environments
  • Effective communication skills, with the ability to clearly convey information across diverse teams and stakeholders
  • Experience contributing to or managing study documentation
  • Proactive problem-solving skills and ability to adapt in a dynamic environment
  • Working knowledge of ICH/GCP and applicable regulatory guidelines
  • Experience working with vendors and cross-functional teams
  • Familiarity with clinical systems such as EDC, IVRS/IWR, CTMS, and Microsoft Office tools

Company info

  • Avalo Therapeutics is a clinical stage biotechnology company fully dedicated to developing therapeutics targeting the IL-1β pathway for immune-mediated inflammatory diseases.

This listing is sourced directly from Avalo Therapeutics's careers page and normalized into a canonical job model.