Cambridge, MA

Our Opportunity…

Obsidian Therapeutics is seeking a Clinical Trial Associate to work alongside the Clinical Development/Operations team to drive forward our clinical trials (currently recruiting patients with metastatic melanoma and non-small cell lung cancer). We’re seeking a candidate with 1-3 years of experience in clinical trials, strong attention to detail, exceptional communication, and organizational skills, who thrives in a dynamic environment managing multiple tasks simultaneously.

As part of our Clinical Operations Department, you’ll be a vital part of a highly collaborative team working to achieve Obsidian’s vision by translating innovative science into medical breakthroughs for patients, starting with our lead program OBX-115.

This is a unique opportunity to be a contributor in a well-funded clinical company with blue chip investors, field-leading advisors, best-in-class partners, and an experienced team. You'll help us build a dynamic, innovative, passionate, collaborative, and successful organization focused on delivering transformative therapies in areas of greatest clinical need.

You Will…

• Support the clinical study teams in the execution and delivery of studies.
• Organize, manage, and oversee the Trial Master File to maintain up-to-date regulatory documentation for all research sites.
• Be responsible for study laboratory sample management, including tracking and vendor management support.
• Collect trial information and disseminate it to the internal project team, the CRO, and other stakeholders.
• Schedule and coordinate internal and external study meetings, materials, and agendas; record and disseminate resulting decisions and actions.
• Be responsible for quality control of the eTMF including maintenance and oversight.
• Coordinate and manage version control of clinical documents.
• Assist in the coordination and tracking of clinical supply shipments with external parties.
• Assist in the creation and updating of standardized clinical trial tools, processes, and SOPs for the clinical operations team and cross functionally as needed.
• Organize and maintain tracking systems and tools to support the conduct of a clinical study from start-up to close-out.
• Act as a contact for the study team for designated project communications, correspondence, and associated documentation.
• Assist with invoice tracking, PO creation, and budget management.
• Ensure inspection readiness and provide support to sites to prepare for clinical audits/inspections.
• Prepare and maintain assigned program files.
• Perform administrative tasks to support team members with clinical trial execution, as needed.

You Bring…

Core Qualifications

• BS/BA/RN Degree in a life science or a health-related field is preferred.
• Minimum of at least 1-3 years working on phase I-IV clinical studies within a biopharmaceutical/biotech, CRO, or academic environment.
• Experience and understanding of clinical trial operations, preferably in the oncology and/or cell therapy space.
• Solid knowledge of ICH/GCP and regulatory requirements.
• Enthusiasm for, and successful experience in a fast-paced and evolving environment.
• Proficiency in MS Office Suite (Word, Excel, PowerPoint).
• Exceptional organizational skills and attention to quality and detail.
• Established ability to prioritize and manage multiple tasks simultaneously, identify and resolve issues, and effectively manage timelines to deliver on commitments.
• Experience collaborating in inter-departmental workgroups to create or enhance processes.
• Strong customer service orientation.

Bonus Qualifications

• Proficiency in Microsoft Project and project management programs.

Work location: Hybrid role based in Cambridge, MA