Clinical Job Opportunity at ICON | Apply Now
Clinical job seekers looking for exciting opportunities in the pharmaceutical and biotechnology industry can explore this excellent opening at ICON Careers. ICON is hiring a Clinical Data Coordinator I for its hybrid role in Warsaw, Poland. This job in Poland is ideal for candidates with a Master’s degree in Life Sciences or Healthcare who have an interest in clinical data management, clinical research, and healthcare innovation.
- Job Position:Â Clinical Data Coordinator I
- Location: Warsaw, Poland (Hybrid)
- Job ID: JR154766
About the Company
Clinical job opportunities at ICON Careers 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 innovation and excellence. The company fosters an inclusive workplace where employees contribute to shaping the future of clinical development. ICON values diversity, collaboration, and professional growth while delivering high-quality clinical research services worldwide.
Clinical Job Description
Clinical job responsibilities at ICON involve supporting clinical data management activities to ensure high-quality clinical research deliverables. As a Clinical Data Coordinator I, you will design and analyze clinical trials, interpret complex medical data, and contribute to the advancement of innovative treatments and therapies. You will work closely with the clinical data management team to ensure quality, compliance, and timely project completion.
Qualifications
Clinical job applicants should possess the following educational qualifications, knowledge, and skills.
Required Education
Master’s degree in Life Sciences, or a relevant field.
Required Skills and Experience
- Basic knowledge of clinical data management within the pharmaceutical or biotechnology industry.
- Familiarity with data management software such as Medidata, Oracle RDC, or similar systems.
- Strong attention to detail.
- 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 added advantage.
Clinical Job – Key Responsibilities
Clinical job responsibilities include supporting clinical data management activities and ensuring study quality throughout the research process.
- Assist the Data Management Study Lead in developing eCRFs, 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 scientists, and functional management as required.
- Perform project-related activities to ensure study timelines are achieved, including filing and archiving study documentation and dispatching investigator queries for resolution.
Clinical job opportunities like the Clinical Data Coordinator I position at ICON Careers offer an excellent pathway for professionals looking to build a successful career in clinical research and data management. This job in Poland provides the chance to work with a globally recognized organization while contributing to innovative healthcare solutions. If you have the required qualifications and a passion for clinical development, this hybrid role in Warsaw could be the perfect opportunity to advance your career in the pharmaceutical and biotechnology industry. Apply today and take the next step toward a rewarding future with ICON.
