Configuration & QC Specialist- Farmingdale NY- Hybrid
We are currently seeking a Configuration & QC Specialist I to join our diverse and dynamic team. As a Configuration & QC Specialist I at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
What you will be doing
- Assisting in the configuration and setup of clinical trial databases and electronic data capture (EDC) systems, ensuring accuracy and adherence to project specifications.
- Performing quality control (QC) checks on clinical trial data and study documentation to identify discrepancies, inconsistencies, and data entry errors.
- Collaborating with cross-functional teams including data management, biostatistics, and clinical operations to address QC findings and ensure data integrity and reliability.
- Supporting the development and implementation of validation plans and procedures to assess the functionality and performance of EDC systems and data management processes.
- Providing training and support to end-users on system configuration, data entry guidelines, and QC processes to promote compliance and efficiency.
Your profile
- Bachelor's degree in life sciences, computer science, or related field; advanced degree preferred.
- 1+ years of experience in clinical data management, data entry, or related role, preferably within the pharmaceutical or biotechnology industry.
- Familiarity with clinical trial databases and electronic data capture (EDC) systems, such as Medidata Rave, Oracle Clinical, or Inform.
- Strong attention to detail and analytical skills, with the ability to identify and resolve data-related issues.
- Excellent communication and interpersonal skills, with the ability to work effectively in a team-oriented environment.
- Proactive attitude with a willingness to learn and adapt to evolving technologies and processes.
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