TScan Therapeutics

Accounting Manager

• Lead preparation of the Company’s Form 10-K
• Collaborate with the Controller, Associate Director SEC Reporting, COO and Legal to ensure filings are complete and accurate
• Assist with earnings releases and Form 8-Ks
• Prepare and/or review supporting external reporting schedules
• Coordinate and manage the annual external audit and supporting consultant relationships
• Manage reporting timelines and communicate them to stakeholders
• Assist with Audit Committee agenda oversight and meeting materials
• Support proxy statement preparation as time allows
• Manage review of the annual tax provision and disclosures prepared by external consultants
• Conduct and document technical accounting research and conclusions
• Collaborate with consultants on complex and judgmental technical accounting matters
• Support the accounting team and monthly close processes, including revenue, leases and investments
• Monitor emerging accounting pronouncements, assess applicability, support implementation and communicate guidance
• Manage development, improvement and implementation of accounting policies and procedures
• Lead year-end SOX 404(a) compliance supporting 10-K SOX conclusions
• Review SOC 1 reports for key vendors and service organizations
• Work with a third-party consultant to finalize SOX testing
• Support Disclosure Committee agendas and materials
• Determine financial statement materiality and posting thresholds
• Complete ad hoc projects with the Corporate Controller

Explore SEC Reporting, Technical Accounting Consultant at TScan Therapeutics. Review requirements and application details.

SEC Reporting, Technical Accounting Consultant

Clinical Research

• Interpret clinical data to generate high-quality summaries and insights supporting regulatory filings, publications, and scientific communications
• Collaborate cross-functionally with Medical Directors, Clinical Operations, Data Management, Biostatistics, and Business Operations across clinical phases
• Lead or support authoring selected sections of clinical study reports in partnership with Medical Directors
• Support real-time data review, identify safety and efficacy trends, assess protocol compliance, and review protocol deviations
• Escalate appropriate issues to Medical Monitors
• Identify scientific and clinical quality issues for discussion with principal investigators and study sites
• Partner with study teams and GCP quality team members on escalations
• Consult on study-specific case report form design and author CRF completion guideline sections
• Ensure CRFs align with study requirements during user acceptance testing
• Perform safety and efficacy reviews for Data Monitoring Committee preparation
• Analyze trends within and across clinical programs
• Collaborate with Business Operations and Data Management on clinical data technology access, retention, and visualization strategy
• Support integration of new tools and technologies into phase 1-3 clinical studies

Explore Clinical Scientist – Consultant at TScan Therapeutics. Review requirements and application details.

Clinical Scientist – Consultant

Content Writer

• Lead planning and management of regulatory submission components from preclinical through registration phases
• Author or coordinate clinical protocols and amendments, Investigator's Brochures, Development Safety Update Reports, clinical study reports, health authority meeting requests and briefing documents, and IND, CTA, CTR, and NDA summary documents
• Manage external resources and coordinate communication with internal contributors and stakeholders
• Serve as lead author and/or document expert for critical deliverables
• Represent Regulatory Writing on cross-functional teams with subject matter experts, Regulatory Affairs, and Program Management
• Develop, maintain, and improve SOPs, authoring guides, and project management tools
• Support submission-related activities with Regulatory Affairs
• Build relationships with Regulatory colleagues, cross-functional project teams, and external stakeholders to achieve timelines and portfolio deliverables

Explore Director, Regulatory Writing at TScan Therapeutics. Review requirements and application details.

Director, Regulatory Writing

Consultant

• Provide clinical pharmacology input to regulatory documents
• Participate in clinical study design and documentation, including lab manuals, protocols, and SAPs
• Independently lead and oversee analysis, interpretation, integration, and reporting of clinical pharmacokinetic and pharmacodynamic data for assigned projects
• Collaborate with Clinical Development, Biostatistics, Non-Clinical Product Development, Clinical Operations, and Regulatory
• Monitor CRO and external vendor work for compliance with protocols, quality standards, and timelines
• Report directly to the Head of Clinical Pharmacology

Explore Clinical Pharmacology Consultant at TScan Therapeutics. Review requirements and application details.

Open roles

SEC Reporting, Technical Accounting Consultant

Clinical Scientist – Consultant

Director, Regulatory Writing

Clinical Pharmacology Consultant