Clinical Data Assoc I at CTI CLINICAL TRIAL & CONSULTING GLOBAL

Cairo, Cairo, Egypt -

Full Time

Start Date

Immediate

Expiry Date

01 Aug, 26

Salary

0.0

Posted On

03 May, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical data management, CRF data review, Database testing, Data query management, ICH/GCP guidelines, Regulatory compliance, Oracle Clinical, Medidata, OmniComm TrialMaster, IBM Clinical Development, Medical coding, Database development, Data documentation, Quality management

Industry

Research Services

Description

What You'll Do: * Review and issue queries for CRF data, based on automated edit checks, manual review, post-hoc data listings, and sponsor requirements * Perform functional testing of project databases. * Ensure the accuracy of project databases as compared to the CRF and the result of any data queries. * Prepare study specific status reports. * Assist with the set-up of data management study files and the collection, transfer and archiving of study documentation and controlled documents. * Maintain all the necessary documentation to support accuracy and integrity of project databases. * Perform all duties according to CTI Standard Operating Procedures (SOP’s) and project specific conventions within the framework of Quality Management and Good Clinical Practice (GCP)/ ICH guidelines. * Maintain accurate records of all work performed Potential Additional Functions: * Medical Coding * Database development and programming What You'll Bring: * Bachelor’s degree or equivalent in biological, behavioral, computer science; or 2 years clinical research experience * 0-2 years scientific research experience in any capacity. * Experience with Oracle Clinical, Medidata, OmniComm TrialMaster, and IBM Clinical Development * Experience providing knowledge of ICH/GCP guidelines and applicable regulatory requirements About CTI * Advance Your Career We invest in your professional growth. Our structured mentoring program, leadership development courses, and dedicated training department provide the support you need to excel. We also encourage ongoing education to help you achieve your professional goals. * Join an Award-Winning Team – Join a global team spanning 60 countries, recognized for its award-winning culture that prioritizes people. We support your work-life balance with hybrid work opportunities. Through our CTI Cares program, you’ll have opportunities to give back to your community and the world. * Make a Lasting Impact At CTI, your work directly contributes to advancing medicine. You’ll play a vital role in developing life-changing treatments for patients with chronic and critical illnesses. Together, we move medicine forward, making a difference for those who need it most. 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 [http://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

Responsibilities

The Clinical Data Associate will review and query CRF data while ensuring the accuracy and integrity of project databases. They will also assist with study documentation, status reporting, and perform functional testing of databases according to SOPs.