CDC Job Opportunity at ICON | Apply Now
CDC job seekers looking for a promising opportunity in clinical research can explore this exciting Clinical Data Coordinator I position at ICON in Warsaw, Poland. This hybrid role offers an excellent opportunity for life sciences graduates and early-career professionals to gain hands-on experience in clinical data management while contributing to innovative clinical development programs within a globally recognized healthcare organization.
- Job Position: Clinical Data Coordinator I
- Job ID: JR148261
- Location: Warsaw, Poland
- Department: Clinical Data Management – ICON Strategic Solutions (FSP)
About the Company
CDC job opportunities at ICON provide professionals with the chance to work for one of the world’s leading healthcare intelligence and clinical research organizations. ICON plc is a global clinical research organization dedicated to advancing healthcare through innovative clinical development solutions. The company fosters an inclusive workplace culture focused on innovation, excellence, diversity, and professional growth. ICON supports pharmaceutical, biotechnology, and healthcare organizations worldwide by delivering high-quality clinical research services.
CDC Job Description
CDC job responsibilities involve supporting clinical data management activities for clinical studies while ensuring data quality and compliance with industry standards. As a Clinical Data Coordinator I, 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. This role offers exposure to various clinical data management processes and collaboration with multidisciplinary teams.
CDC Job – Qualifications
- Master’s degree in a relevant field such as Life Sciences.
- Candidates in the final stage of their Master’s studies will also be considered.
- Availability to start work in July.
- Basic knowledge of clinical data management within the pharmaceutical or biotechnology industry.
- Familiarity with data management software and systems such as Medidata, Oracle RDC, or similar platforms.
- Strong attention to detail and ability to work effectively in a fast-paced environment.
- Excellent communication and collaboration skills.
- Knowledge of regulatory guidelines and standards such as ICH-GCP is an advantage.
Preferred Skills
- Clinical data review and validation experience.
- Understanding of clinical trial processes.
- Knowledge of data management systems.
- Strong organizational abilities.
- Effective teamwork and communication skills.
- Problem-solving mindset and attention to detail.
CDC Job – Key Responsibilities
- Assist Data Management Study Lead in development of eCRF, Data Validation Specifications, and Study Specific Procedures.
- Review clinical and third-party data based on edit specifications and data review plans.
- Issue clear, accurate, and concise queries to investigational sites.
- Communicate effectively with peers, clinical data scientist, and functional management as required.
- Perform additional project activities to ensure study timelines are met.
- Support filing and archiving of study documentation.
- Dispatch queries to investigator sites for timely resolution.
- Maintain data quality and study compliance throughout project execution.
Why Join ICON?
CDC job seekers interested in a long-term career in clinical research can benefit from ICON’s commitment to professional development, diversity, and inclusion. ICON values innovation, collaboration, and excellence while providing employees with opportunities to work on impactful clinical studies that contribute to the development of new treatments and therapies worldwide.
