Clinical Trial Associate – Oncology

Obsidian Therapeutics

Clinical Trial Associate supporting oncology clinical trials at Obsidian Therapeutics. Coordinating clinical trial operations and ensuring compliance with protocols and regulations.

Posted 7/16/2026full-timeBedford • Massachusetts • 🇺🇸 United StatesJuniorMid-Level💰 $92,000 - $112,500 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial operations, including maintaining Trial Master Files, ensuring regulatory compliance, and coordinating with internal teams and external partners. Proficient in tracking study activities, managing vendor performance, and facilitating effective communication across stakeholders.

Highest-signal resume keywords

Clinical Trial OperationsTrial Master File ManagementICH/GCP KnowledgeVendor CoordinationBiospecimen Tracking

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study ManagementData Accuracy AssuranceQuality Control ActivitiesStudy Tracking Tool DevelopmentAudit Preparation Support

Soft Skills

Effective CommunicationTeam CoordinationProblem-Solving

Tools & Technologies

Study Tracking ToolsDocument Management Systems

Industry Keywords

BiopharmaceuticalBiotechCROOncologyCell Therapy

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Support day-to-day clinical trial operations in alignment with protocols, timelines, and regulatory requirements.
Serve as a point of coordination across internal teams, CROs, and external partners.
Maintain the Trial Master File (TMF), ensuring completeness, accuracy, and audit readiness.
Perform TMF quality control activities and proactively address gaps.
Support audits and inspections, including preparation and follow-up activities.
Coordinate with vendors, including central labs and specialty service providers.
Support biospecimen tracking, logistics, and associated documentation.
Track and monitor vendor performance and escalate issues as needed.
Develop, maintain, and improve study tracking tools (e.g., enrollment, sample tracking, timelines).
Ensure data accuracy and timely reporting across study activities.
Contribute to improvements in clinical operations processes and systems.
Facilitate clear, timely communication across study teams and stakeholders.
Coordinate study meetings, including agenda development, minutes, and follow-up actions.
Maintain version control and documentation across clinical materials.
Support invoice tracking, purchase order coordination, and budget-related activities.

Requirements

What you’ll need

BS/BA/RN Degree with 3+ years of experience in a life science or a health-related field is preferred.
1+ 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 oncology and/or cell therapy space.
Solid knowledge of ICH/GCP and regulatory requirements.

Benefits

Comp & perks

Comprehensive medical, dental, and vision coverage
Company contributions to health savings and retirement accounts
Ample paid time off
Access to wellness programs
Rich career growth opportunities
Annual incentive bonus as a percentage of actual base salary
Long-term incentives in the form of employee stock options