Senior Clinical Research Associate

TFS HealthScience - Contract Research Organization

Join TFS HealthScience as a Senior Clinical Research Associate overseeing clinical trials. Collaborate with teams and ensure compliance with GCP and regulatory standards for dermatology projects.

Posted 7/1/2026full-timeRemote • Connecticut, Maine, Massachusetts, New Hampshire, Rhode Island, Vermont, Washington • 🇺🇸 United StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

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

Demonstrates expertise in Clinical Research Associate (CRA) responsibilities, including on-site monitoring, data quality assurance, and regulatory compliance. Proficient in managing trial documentation systems and collaborating with project teams to ensure timely deliverables.

Highest-signal resume keywords

CRA ExperienceGCP UnderstandingICH KnowledgeMonitoring Visit ReportingInvestigational Product Accountability

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ResearchData Quality AssuranceProtocol ComplianceMonitoring Visit PreparationETMF ManagementCTMS ManagementSource Documentation ReviewInformed Consent ProceduresIssue ResolutionRegulatory Requirements

Soft Skills

Excellent CommunicationOrganizational SkillsAttention to DetailProblem-Solving MindsetCollaborative Work

Industry Keywords

Life SciencesNursingDermatologyFast-Paced EnvironmentMatrix Organization

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Perform on-site and remote monitoring visits to ensure subject safety and data quality
Review CRFs and source documentation for accuracy and completeness
Ensure informed consent procedures and protocol compliance are met
Manage and track Investigational Product accountability
Prepare monitoring visit reports and follow up on action items
Maintain and update eTMF, CTMS, and trial documentation systems
Support sites with issue resolution and ensure timely completion of deliverables
Participate in audits and inspections, including preparation and follow-up
Collaborate with project teams and contribute to monitoring plans, project tracking, and CRA resource planning

Requirements

What you’ll need

Bachelor’s degree in Life Sciences, Nursing, or equivalent
Minimum 3+ years of CRA experience, including on-site monitoring
Strong understanding of GCP, ICH, and regulatory requirements
Experience working in a fast-paced, matrix organization
Excellent communication and organizational skills
Fluent in English
Strong attention to detail and problem-solving mindset
Ability to work independently and collaboratively
Experience in dermatology is considered a strong advantage.

Benefits

Comp & perks

Competitive compensation package
Comprehensive benefits
Opportunity for personal and professional growth
Supportive work environment