Job Purpose Summary:
Work with clinical research coordinators and investigators to preform appropriate clinical assessments for clinical trials (e.g., clinical safety labs, vital signs, ECGs, PK, etc.) from pre-study planning through successful completion of all subject visits and documentationWhat you'll do:
Responsible for the collection, processing and shipment of laboratory samples in accordance with site Standard of Procedures (SOPs), Clinical Trial Protocol, and Good Clinical Practice specifications Obtain vital signs; perform ECGs and other clinical procedures Work closely with Clinical Research Coordinators to complete source documentation, case report forms and other study specific documents completely, accurately and in accordance with site SOPs, Clinical Trial Protocol, and Good Clinical Practice specifications Assist Clinical Research Coordinators with coordinating subject care visits.
Work closely with Clinical Research Coordinators and Management to learn and enhance clinical research knowledge Comply with Good Clinical Practices at all times Behave in a cooperative and constructive manner; follow all company policies, state, local, federal and other applicable laws and guidelines; comply with all job-specific requirements What you'll bring:
Proficient in phlebotomy skills Proficient in performing ECGs, vital signs, and processing specimens Detail oriented Ability to work well in a team environment Ability to maintain confidentiality Ability to develop, prioritize, organize and manage multiple tasks1-2 years of experience as a medical assistant, phlebotomist or in a similar position within the medical or mental health field High school diploma or equivalent Preferred - Medical Assistant and/or Phlebotomy CertificationAbout CTICTI 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
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 NoteIn 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 ( or from our verified LinkedIn page.
Please NoteWe will never communicate with you via Microsoft Teams or text messageWe will never ask for your bank account information at any point during the recruitment process
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Job Purpose Summary: • Work with clinical research coordinators and investigators to preform appropriate clinical assessments for clinical trials (e.g., clinical safety labs, vital signs, ECGs, PK, etc.) from pre-study planning through successful completion of all subject visits and...