eTMF Analyst I (Trial Master File Management)

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.

• →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

• 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

• 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

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

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.

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