CDC Job Opportunity at ICON | Apply Now
CDC job opportunities are growing rapidly in the clinical research industry, and ICON plc is now hiring a Clinical Data Coordinator II for its teams in Taipei and Dalian. This exciting life sciences job offers professionals the opportunity to work in clinical data management, support innovative clinical trials, and contribute to the future of healthcare research. Candidates with experience in clinical data management, healthcare, or biotechnology can explore rewarding career growth through ICON careers.
- Job Title: Clinical Data Coordinator II
- Location: Taipei, Dalian
- Job ID: JR137355
- Department: Clinical Data Management, ICON Strategic Solutions (FSP)
About the Company
CDC job opportunities at ICON plc provide professionals with a chance to work with a world-leading healthcare intelligence and clinical research organization. ICON plc is known for fostering an inclusive environment that drives innovation and excellence in clinical development. The company supports employee growth, diversity, and well-being while contributing to the advancement of innovative treatments and therapies worldwide.
ICON careers offer employees competitive benefits, flexible work-life balance opportunities, healthcare coverage, retirement planning support, and global employee wellness programs.
CDC Job Description
CDC job responsibilities at ICON careers involve supporting clinical data management activities and contributing to successful clinical trial execution. The Clinical Data Coordinator will work closely with project teams, clinical data scientists, and functional management to ensure accurate and efficient clinical data processing.
As part of this life sciences job, candidates will play an important role in maintaining eCRF systems, managing clinical data reconciliation, and supporting study-specific procedures in a fast-paced pharmaceutical and biotechnology environment.
Qualifications
CDC job applicants should meet the following qualifications:
- Bachelor’s degree in a relevant field such as Life Sciences or Healthcare.
- Intermediate 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 the ability to work effectively in a fast-paced environment.
- Excellent communication skills and the ability to collaborate with cross-functional teams.
- Knowledge of regulatory guidelines and standards such as ICH-GCP is a plus.
Benefits at ICON Careers
- Various annual leave entitlements
- Health insurance offerings for employees and families
- Competitive retirement planning programs
- Global Employee Assistance Programme, LifeWorks
- Life assurance coverage
- Flexible country-specific optional benefits
- Childcare vouchers
- Discounted gym memberships
- Subsidized travel passes
- Health assessments and wellness support
Key Responsibilities
CDC job duties include:
- Assist the Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures.
- Manage clinical and third-party data reconciliation based on edit specifications and data review plans.
- Track and communicate study and task metrics to clinical data scientists, project teams, and functional management.
- Address data-related questions and recommend potential solutions.
- Identify root causes to systematically resolve data issues.
- Support accurate clinical data collection and validation processes.
- Collaborate with cross-functional teams within the organization.
Why Apply for This CDC Job?
CDC job openings at ICON plc provide professionals with the opportunity to work on innovative clinical research projects while building a strong career in clinical data management. Candidates looking for jobs in Taiwan & China can benefit from global exposure, collaborative work culture, and long-term career development opportunities through ICON careers.
