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eTMF Analyst I (Trial Master File Management)

Role overview

Qualifications

  • Associate degree in allied health field such as nursing, pharmacy, or health science or equivalent relevant experience
  • 1-2 years of experience in pharmaceutical, site, or CRO service
  • Ongoing willingness to learn
  • Detail oriented

Responsibilities

  • Organize, manage, and maintain electronic trial documentation according to CTI SOPs or Sponsor SOPs/PSOPs and ICH/GCP guidelines
  • Analyze and process trial documents electronically by performing a quality review for deficiencies
  • Sync documents and apply metadata according to the TOC and eTMF plan
  • Provide data analysis, complete a quality review process, and file documents while managing multiple eTMF systems

Key facts

Hard skills

Other skills

  • Quality Control
  • Detail Oriented
  • Customer Service
  • Non-Verbal Communication

About the company

CTI Clinical Trial and Consulting Services logo

CTI Clinical Trial and Consulting Services

Contract Research Organizations (CRO)

CTI Clinical Trial and Consulting Services is a global, privately held, full-service contract research organization (CRO), delivering a complete spectrum of clinical trial and consulting services throughout the lifecycle of development, from concept to commercialization. CTI’s focused therapeutic approach provides pharmaceutical, biotechnology, and medical device firms with clinical and disease area expertise in rare diseases, regenerative medicine/gene therapy, immunology, transplantation, nephrology, hematology/oncology, neurology, infectious diseases, hepatology, cardiopulmonary, and pediatric populations. CTI also offers a fully integrated multi-specialty clinical research site that conducts phase I-IV trials. CTI has a passion for helping life-changing therapies succeed in chronically and critically ill patient populations. With clinical trial experience across 6 continents, CTI partners with research sites, patients, and sponsors to fulfill unmet medical needs. CTI is headquartered in Cincinnati, OH, with operations across North America, Europe, Latin America, and Asia-Pacific. For more information visit www.ctifacts.com

Company details

IndustryContract Research Organizations (CRO)
Company size1001 - 5000

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Job description

About the job:

Responsible for assisting with the analysis and management of essential trial documentation for multiple regulated projects and developing skills to successfully and efficiently analyze and quality control (QC) individual trial/project specific essential regulatory documents.

What You'll Do:

  • Organize, manage, and maintain electronic trial documentation according to CTI SOPs or Sponsor SOPs/PSOPs and ICH/GCP guidelines
  • Become proficient in the eTMF Reference Model Table of Contents (TOC) and document types listed in the TOC
  • Analyze and process trial documents electronically by performing a quality review for deficiencies, resolve discrepancies by using standard procedures or returning incomplete documents for resolution
  • Sync documents and apply metadata according to the TOC and eTMF plan
  • Provide data analysis, complete a quality review process, and file documents while managing multiple eTMF systems
  • Perform content review as it pertains to each individual document type to ensure correct filing against trial specific TOC in the eTMF
  • Verify accuracy of document electronic filing location by reviewing, correcting, deleting, or re-entering data
  • Provide dedicated support for individual assigned eTMF, but also assist as needed for all trial eTMF filing
  • Retain and apply trial specific knowledge to several eTMFs as directed by the sponsor preference and use
  • Maintain accurate eTMFs by interacting with trial team members to resolve issues and inconsistencies
  • Retain and update job specific training tools and guides (via OneNote, SharePoint, etc.) to ensure quality document processing
  • Utilize electronic tools (i.e., CTI Business Intelligence, SSRS, etc.) to stay ahead and track filing timelines for individual trials and escalate observed issues in timelines or specific documents
  • Assist with annual quality reviews and re-classify/edit document metadata per trial team instruction

What You'll Bring:

  • Associate degree in allied health field such as nursing, pharmacy, or health science or the equivalent relevant experience
  • 1-2 years of experience in pharmaceutical, site, or CRO service

Competencies:

  • Ongoing willingness to learn
  • Detail oriented
  • Ability to collaborate well in a team environment
  • Ability to maintain confidentiality
  • Strong computer skills
  • Ability to provide a superior level of customer service
  • Ability to prioritize, organize, and manage multiple tasks
  • Basic awareness of and willingness to learn GCP, FDA regulations, and ICH guidelines
  • Excellent verbal and written communication skills

About CTI

CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com

Why CTI?

Advance Your Career – We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through tuition reimbursement and a dedicated training department.
Join an Award-Winning and Valued Team – We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering generous health benefits and vacation packages, hybrid work from home opportunities, and paid parental leave. We also encourage care for the world around us through our unique CTI Cares program.
Make a Lasting Impact – We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market.

Important Note
In light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from an @ctifacts.com email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website (www.ctifacts.com) or from our verified LinkedIn page.

Please Note

We will never ask for your bank account information at any point during the recruitment process

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Marcus Rivera

Chief Revenue Officer

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