CDC Job Opportunity at ICON | Apply Now
CDC job opportunities are growing rapidly in the global clinical research industry, and this exciting role at ICON plc offers aspiring clinical data professionals a chance to build a rewarding career in clinical data management. This hybrid opportunity in Warsaw is ideal for life sciences and healthcare graduates looking to gain experience in the pharmaceutical and biotechnology industry while working with innovative clinical research teams.
- Job Title: Clinical Data Coordinator
- Location: Warsaw, Poland
- Job Reference: JR151925
- Department: Clinical Data Management
- Division: ICON Strategic Solutions (FSP)
About the Company
CDC job opportunities at ICON plc provide professionals with a chance to work in one of the world’s leading healthcare intelligence and clinical research organizations. ICON plc is globally recognized for supporting clinical development, medical innovation, and healthcare research across multiple therapeutic areas.
The company focuses on building an inclusive workplace culture that promotes innovation, collaboration, and excellence. Through its strategic solutions and functional service provider (FSP) model, ICON supports pharmaceutical and biotechnology companies in advancing clinical trials and delivering life-changing therapies worldwide. Professionals searching for ICON Careers and life sciences jobs can benefit from the company’s strong global reputation, career growth opportunities, and employee-focused work environment.
CDC Job Description
CDC job responsibilities at ICON involve supporting clinical data management activities for clinical trials and healthcare research projects. The Clinical Data Coordinator will work closely with data management study leads and cross-functional clinical teams to ensure accurate and timely clinical data review.
This life sciences job is suitable for candidates interested in clinical research, biotechnology, pharmaceutical data management, and healthcare analytics. The selected candidate will contribute to clinical trial operations by reviewing data, managing queries, supporting electronic Case Report Forms (eCRFs), and ensuring compliance with industry standards and regulatory guidelines.
Qualifications Required
CDC job eligibility criteria include:
- Master’s degree in Life Sciences or a related field.
- Candidates in the final stage of their Master’s studies may also be considered.
- Availability to commence work in July.
- Ability to work in a hybrid setup in Warsaw, Poland.
- Basic understanding of clinical data management in the pharmaceutical or biotechnology industry.
- Familiarity with data management systems such as Medidata, Oracle RDC, or similar platforms.
- Strong attention to detail and ability to work in a fast-paced environment.
- Excellent communication and teamwork skills.
- Knowledge of ICH-GCP regulatory guidelines is considered an advantage.
Skills Preferred
CDC job applicants with the following skills may have an added advantage:
- Clinical data review expertise
- Understanding of clinical trial workflows
- Knowledge of healthcare research standards
- Data validation and query management skills
- Strong organizational abilities
- Cross-functional collaboration skills
- Problem-solving and analytical thinking
Key Responsibilities
CDC job duties and responsibilities include:
- Assist the Data Management Study Lead in developing electronic Case Report Forms (eCRFs), Data Validation Specifications, and Study Specific Procedures.
- Review clinical and third-party data according to edit specifications and data review plans.
- Issue clear, accurate, and concise queries to investigational sites.
- Communicate effectively with peers, clinical data scientists, and functional management teams.
- Support project activities to ensure study timelines are achieved.
- Perform filing and archiving of study documentation.
- Dispatch queries to investigator sites for resolution.
- Maintain accuracy and consistency in clinical trial data management activities.
Why Choose This CDC Job?
CDC job roles at ICON provide excellent exposure to the global clinical research industry. Candidates can gain hands-on experience in clinical data management, pharmaceutical research, biotechnology operations, and healthcare intelligence.
This role is especially beneficial for fresh graduates and early-career professionals aiming to establish themselves in clinical research and life sciences careers. Working with an internationally recognized organization like ICON plc can significantly strengthen professional growth and future opportunities in the biotechnology and pharmaceutical sectors.
