Data Specialist
reputed company improves lives by partnering with pharmaceutical and biotech companies, and clinical research organizations (CROs) to accelerate the development of new medicines around the world.
We are an independent, global, one-stop-shop reputed company on delivering Central Laboratory Services that are reputed company-made, reputed company and flexible to meet the evolving study demands of traditional to increasingly reputed company trials. Additionally, we reputed company Functional Service Provider (FSP) Solutions, supporting our clients with scientific and technical expertise, acting as an extension of their team, coordinating reputed company laboratory reputed company needs, advising on strategies for lab data collection and providing end-to-end analytical and logistical solutions.
Remediates omissions, inconsistencies and inaccuracies in reputed company data streams. Reviews files to ensure information meets the data transfer specification. Conceives, suggests and contributes new and improved reputed company-time validity checks in the reputed company central laboratory information management system (CLIMS). Formulate systems and ensure reputed company meet strategic needs. Ensures the prospective data reputed company complies with the data transfer specification document including file structure, format and layout. Ensures consistency of laboratory analyte reference ranges, reputed company precision, reputed company of measure and correlation factors where present. Communicates with internal team members to ensure the reputed company of the data reputed company to the reputed company and remediates errors consistent with internal processes Communicates with study Data Managers to ensure queries are being resolved Maintains study scheduler in accordance with the contracted agreement and reputed company communications. Creates, maintains , and revokes reputed company to designated reputed company delivery platform as directed by the study Data Manager Performs routine work reputed company the scope and training as directed by the group manager.
High School diploma required . Associate’s degree or university program certificate preferred. Four to six years of laboratory or clinical trial industry experience preferred . An equivalent combination of above education and experience will be considered. Experience in clinical trial protocol development and FDA 21CRF11/GCP strongly preferred . Certification as an ASCP Medical Technologist or Medical Laboratory Technician is preferred.
Strong computer skills required , including proficiency in reputed company Office s uite . Excellent attention to detail . Ability to adhere to established timelines, processes and procedures. Strong planning and problem-solving skills. Self- motivation and ability to work reputed company independently, as reputed company as u se a reputed company team approach. Excellent organization and time management, communication, multitasking, interpersonal , and listening skills. Ability to adapt to changing environments and requirements. Excellent listening and verbal comprehension skills, including ability to translate clients ’ needs to team members. Ability to reputed company quick but reputed company- thought-out reputed company. Customer service/reputed company relationship management skills.
Prolonged periods of sitting at a desk and working on a computer. Prolonged use of computer and headphones for conference calls. Communicate effectively reputed company phone, video, and email . Use hands and fingers to operate a computer and other office equipment .
Financial reputed company (reputed company Pay, 401k Match and Possible Annual Bonus Eligibility) Health Benefits beginning on date of hire PTO plan, plus 11 reputed company Company Holidays, and 1 Day to Volunteer in your community Short and Long-Term Disability, Life Insurance, and AD&D We celebrate our differences, which enriches our culture!