[Hiring] Clinical Data Specialist @Cordis

Role Description

This remote-based EU position plays an important role in the success of SELUTION clinical trials and contributes to improving patient care by ensuring the quality of clinical data collected from clinical study sites. The Clinical Data Specialist supports the collection, processing, and review of clinical trial data across SELUTION DEB studies. Working under the guidance of the Clinical Data Manager, this role assists in day‑to‑day data management activities to ensure high-quality, reliable clinical data throughout the lifecycle of a trial.

• Assist with database setup activities
• Support the development of case report forms
• Perform data entry checks
• Generate and resolve data queries
• Contribute to ongoing data cleaning
• Collaborate closely with the Clinical Data Manager, study management teams, clinical sites, and external partners

Qualifications

• Global pre-market and post-market medical device clinical study experience is required
• Bachelor’s degree or equivalent
• Minimum of 3 years’ clinical experience in Medical Device studies
• Minimum of 3 years’ clinical data management experience, with experience using and developing multiple clinical data management systems
• Data management experience on global pre-market and post-market studies (including US IDE trials)
• Experience as database programmer

Requirements

• Precise, Rigorous, Detail-Oriented
• Outstanding verbal and written communication skills, in addition to excellent organizational skills
• Strong interpersonal skills, with the ability to collaborate effectively and maintain professional interactions
• Problem-solving abilities, with the capacity to recognize issues and escalate them appropriately to the Clinical Data Manager
• Supportive team member, keen to promote quality through example and continuous support
• Team‑oriented mindset, demonstrating reliability and a positive approach to supporting group goals
• Ability to thrive in a fast-paced environment while remaining flexible, proactive, resourceful and efficient
• Knowledgeable in ICH GCP guidelines and industry standards applicable to data capture and data management process to ensure the appropriate conduct of clinical studies
• Familiarity in Power BI, Smartsheet, or other data/dashboard tools
• Comfortable working in an international environment, with an appreciation for global clinical trial operations
• Fluent in English (additional languages are beneficial)

Benefits

• Cordis is proud to be an equal opportunity employer
• Committed to providing equal opportunity for all teammates and applicants
• Diversity includes race, gender identity, age, disability status, veteran status, sexual orientation, religion, and many other parts of one’s identity
• Strive to create and maintain working and learning environments that are inclusive, equitable and welcoming