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Sr Clinical Data Associate

Role overview

Qualifications

  • 3 to 4 years clinical data management experience in any capacity
  • 2 years relational database experience
  • Bachelor’s Degree or equivalent in biological, behavioral, or computer science

Responsibilities

  • Conduct pre-entry review of clinical data
  • Review and issue queries for case report form (CRF) data based on automated edit checks, manual review, and sponsor requirements
  • Assist with set-up of data management study files and the collection, transfer, and archiving of study documentation
  • Collaborate with management to develop and refine departmental SOPs relating to data management

Key facts

  • Remote from: Portugal
  • Full time
  • Senior (5-10 years)
  • Clinical Data Analyst
  • English

Hard skills

Other skills

  • Collaboration
  • Detail Oriented
  • Mentorship

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

What You'll Do:

  • Conduct pre-entry review of clinical data 
  • Review and issue queries for case report form (CRF) data based on automated edit checks, manual review, and sponsor requirements 
  • Assist with set-up of data management study files and the collection, transfer, and archiving of study documentation and controlled documents 
  • Maintains all the necessary documentation to support accuracy and integrity of clinical databases 
  • Assist with the tracking of controlled documents (CRFs, data clarification forms [DCFs], etc) 
  • Assist in defining workflow and processes for all aspects of data management 
  • Collaborate with management to develop and refine departmental SOPs relating to data management 
  • Conduct and direct database development, testing, and validation 
  • Conduct and direct training of clinical data associate (CDA) staff 
  • Carry out all activities according to CTI SOPs and project-specific conventions within the framework of Quality Management and Good Clinical Practice (GCP) / ICH guidelines 
  • Maintain accurate records of all work performed  

What You'll Bring: 

  • 3 to 4 years clinical data management experience in any capacity 
  • 2 years relational database experience 
  • Bachelor’s Degree or equivalent in biological, behavioral, or computer science  

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 communicate with you via Microsoft Teams or text message
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

m.rivera@company.com
linkedin.com/in/marcusrivera
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