Clinical Trial Associate

Cardurion Pharmaceuticals

. Support day-to-day operational management of assigned clinical studies, including study start-up, conduct, and close-out activities .

Posted 11/3/2026full-timeBurlington • Massachusetts • United StatesJuniorMid-Level💰 $95,000 - $105,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical study operations, including study start-up, conduct, and close-out activities, while ensuring compliance with ICH-GCP standards. Proficient in document management, vendor coordination, and effective communication within multidisciplinary teams.

Highest-signal resume keywords

Clinical Operations ExperienceICH-GCP KnowledgeETMF and CTMS FamiliarityMS Office ProficiencyVendor Coordination

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study ManagementTrial Master File ReviewDocument Quality ControlStudy Tracker MaintenanceProtocol DevelopmentInformed Consent FormattingMetrics CollectionStudy Plan DevelopmentCRF Completion GuidelinesSubmission Documentation

Soft Skills

Effective Time ManagementExcellent Communication SkillsInterpersonal SkillsSelf-MotivatedOrganizational Skills

Industry Keywords

CRO CoordinationClinical TrialsStudy LogisticsMultidisciplinary TeamsProcess Improvement

About the role

Key responsibilities & impact

Support day-to-day operational management of assigned clinical studies, including study start-up, conduct, and close-out activities
Review and QC-check Trial Master File documents
Track monitoring report receipt and training records
Track vendor deliverables, collect metrics, and file documents
Support multidisciplinary clinical study teams with logistics and follow-up
Communicate with CRO/vendor counterparts on routine logistics
Assist with formatting, version control, QC, and distribution of study documents and plans
Maintain study trackers for study progress, including site start-up, enrollment, and supplies
Review study document templates and site-specific adaptations, including ICFs and patient recruitment materials
Support development of protocols, informed consents, study plans and tools, CRF Completion Guidelines, Clinical Study Reports, and submission documentation
Assist with coordination of DMC and other committees
Schedule internal team meetings and prepare agendas, minutes, and action-item logs
Support investigator meetings and other study-specific meeting logistics
Provide input on SOPs and templates
Manage study system access and user requests
Participate in departmental process improvement initiatives

Requirements

What you’ll need

Proven experience handling confidential and sensitive information with discretion and good judgment
Self-motivated, with initiative and ability to take ownership and follow through on tasks
Effective time management and organization skills; ability to multitask and shift priorities quickly under tight deadlines
Excellent interpersonal, written and verbal communication skills
Ability to develop collaborative internal and external relationships
Ability to communicate, collaborate, and deliver excellent work in a fast-paced, rapidly growing company
Bachelor’s degree in a scientific or health-related field, or equivalent experience
At least 1 year of clinical operations or trial support experience at a Sponsor, or at least 2 years at a CRO
Working knowledge of ICH-GCP
Familiarity with eTMF and CTMS systems
Exposure to CRO and vendor coordination in an outsourced Clinical Trial structure
Proficiency in MS Office (Outlook, MS Word, Excel, PowerPoint)
Some travel may be expected for internal meetings, conferences, or training events

Benefits

Comp & perks

Healthcare coverage including medical, dental and vision
Fully funded Healthcare Savings Account for high-deductible PPO Plan
4 weeks paid time off annually
10 company paid holidays and year-end shut down
401k (traditional and Roth offered) with company match
Company-paid life insurance
Company-paid short-term disability insurance
Company-paid long-term disability insurance
Flexible spending accounts for medical and dependent care expenses