In-House Clinical Research Associate, CRA

Praxis

Clinical Research Associate supporting inspection-ready CNS clinical trials at Praxis Precision Medicines, a clinical-stage biopharmaceutical company. Coordinating sites, documents, compliance, and study deliverables.

Posted 8/17/2026full-timeRemote • 🇺🇸 United StatesJuniorMid-Level💰 $75,000 - $95,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing clinical trial logistics, ensuring compliance with GCP and ICH guidelines, and facilitating effective communication across cross-functional teams. Proven ability to drive process improvements and manage multiple priorities in a fast-paced environment.

Highest-signal resume keywords

Clinical Trial ExperienceGCP KnowledgeRegulatory SubmissionsMicrosoft Office ProficiencyOrganizational Skills

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical Trial ManagementProtocol ComplianceDocument TrackingAction Item ManagementProcess Improvement

Soft Skills

Problem-Solving MindsetAttention to DetailCommunication SkillsTeam PlayerOrganizational Skills

Tools & Technologies

Trial Master FilesMicrosoft WordMicrosoft ExcelMicrosoft PowerPointMicrosoft Outlook

Industry Keywords

BiotechPharmaCROICH GuidelinesRegulatory Requirements

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Support study execution by managing meeting logistics, documenting decisions, and tracking action items
Partner with Clinical Operations and site monitors to ensure protocol compliance and quality standards are met
File site-level documents into Trial Master Files (TMFs) in a timely manner
Track, review, and organize essential documents from sites and vendors
Identify, escalate, and help resolve site-level issues with cross-functional teams
Assist with regulatory submissions and other study deliverables
Drive process improvements that enhance speed, quality, and patient impact

Requirements

What you’ll need

Bachelor’s degree in a life science or health-related field, or equivalent industry experience
5+ years of clinical trial experience in biotech, pharma, or CRO settings
Solid knowledge of GCP, ICH guidelines, and regulatory requirements
Exceptional organizational and communication skills
Proactive, problem-solving mindset with high attention to detail
Comfortable managing multiple priorities in a fast-paced, mission-driven environment
Strong team player who thrives in flat, agile organizations
Proficient in Microsoft Office (Word, Excel, PowerPoint, Outlook)
Comfortable with regular computer/device and office-equipment use, clear communication, occasional movement, screen work, basic hand coordination, and sustained focus

Benefits

Comp & perks

99% of the premium paid for medical, dental, and vision plans
Company-paid life insurance
AD&D benefits
Disability benefits
Voluntary plans to personalize coverage
Dollar-for-dollar 401(k) matching up to 6% on eligible contributions
Long-term stock incentives
ESPP
Discretionary quarterly bonus
Extremely flexible wellness benefit
Generous PTO
Paid holidays
Company-wide shutdowns