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Clinical Trial Assistant, Tmf

Icon
ICON
2-5 years
Not Disclosed
Remote
10 Feb. 19, 2026
Job Description
Job Type: Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Trial Assistant (CTA) – Trial Master File (TMF) Operations | Remote | Multiple U.S. Locations

Job ID: JR140083
Location: Multiple U.S. Locations (Remote)
Department: Clinical Trial Support
Company: ICON Strategic Solutions

ThePharmaDaily.com is featuring an excellent opportunity for a Clinical Trial Assistant (CTA) – TMF Operations with ICON Strategic Solutions, a globally recognized clinical research and healthcare intelligence organization. This remote role across multiple U.S. locations is ideal for clinical research professionals seeking to advance their expertise in Trial Master File (TMF) management, eTMF quality control, and regulatory compliance within a dynamic clinical development environment.

This position is strategically designed for professionals experienced in clinical trial documentation, TMF structure, and inspection readiness. If you are looking to strengthen your career in clinical operations, regulatory documentation, and global clinical trial support, this role offers strong professional growth and cross-functional exposure.

Position Overview

The Clinical Trial Assistant (CTA) will play a critical role in supporting Trial Master File (TMF) operations with a strong focus on eTMF quality control, documentation integrity, and regulatory compliance. The successful candidate will ensure that TMF documentation is complete, accurate, inspection-ready, and aligned with global regulatory standards including ICH-GCP guidelines.

This role requires hands-on expertise in TMF review, cross-document consistency checks, and proactive issue identification to maintain high-quality clinical documentation standards across programs.

Key Responsibilities

  • Perform detailed eTMF quality control (QC) reviews, ensuring completeness, accuracy, and compliance of clinical trial documentation.

  • Evaluate cross-document relationships within the TMF to ensure consistency, alignment, and regulatory adherence.

  • Support inspection readiness by identifying documentation gaps, discrepancies, and quality risks.

  • Provide administrative and operational support to clinical trial teams, including maintaining trial records and tracking documentation milestones.

  • Assist in preparing and submitting regulatory documentation in compliance with study protocols and global regulatory requirements.

  • Collaborate with cross-functional teams including Clinical Operations, Regulatory Affairs, and Data Management to ensure smooth trial execution.

  • Monitor trial progress and facilitate timely communication between study teams and sites.

  • Maintain strong stakeholder relationships to ensure efficient clinical trial documentation processes.

Experience Required

  • Minimum 2–5 years of experience in clinical trial support, TMF management, or eTMF quality control within a CRO, pharmaceutical, or biotech environment.

  • Demonstrated hands-on experience conducting eTMF/TMF quality control reviews, beyond basic administrative filing activities.

  • Strong working knowledge of TMF reference models, regulatory inspection requirements, and ICH-GCP guidelines.

  • Experience supporting inspection readiness activities is highly preferred.

  • Proficiency in Clinical Trial Management Systems (CTMS), eTMF platforms, and document management systems.

Educational Qualifications

  • Bachelor’s degree in Life Sciences, Clinical Research, Healthcare, or a related discipline preferred.

  • Relevant certifications in Clinical Research or Regulatory Affairs are advantageous.

Core Competencies

  • Strong attention to detail with a focus on documentation integrity and compliance

  • Advanced organizational and multitasking skills

  • Excellent written and verbal communication skills

  • Ability to identify documentation inconsistencies and quality risks

  • Cross-functional collaboration and stakeholder management

  • Strong analytical and problem-solving capabilities

Why Consider This Opportunity

  • Remote flexibility across multiple U.S. locations

  • Exposure to global clinical programs and regulatory environments

  • Competitive compensation and comprehensive benefits package

  • Health insurance, retirement planning, life assurance, and employee assistance programs

  • Inclusive and performance-driven organizational culture

  • Career development within a leading global clinical research organization

About ICON Strategic Solutions

ICON Strategic Solutions is part of a global healthcare intelligence and clinical research organization dedicated to accelerating drug development and improving patient outcomes. The organization fosters innovation, diversity, and professional excellence, making it a preferred employer within the clinical research industry.