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The GDS Project Coordinator role focuses on ensuring the accuracy, completeness, and integrity of the clinical trial data and related documentation. This position combines knowledge of clinical research with strong data management, organization and documentation skills. The Project Coordinator is responsible for managing various types of documentation associated with clinical trials within the data science and data management science domains. The Project Coordinator may lead Study timelines discussions and be responsible for organizing meetings, generating meeting agendas and meeting minutes, and provide administrative support within the Global Data Science and Data Management Science groups. The Project Coordinator may also act as Executive Travel Coordinator, Process Improvement Initiative contributor, as needed.
Job Responsibility:
Clinical documentation review
Data quality assurance
Regulatory compliance
Documentation management
Expense Reports + Travel Planning/Scheduling
Study Timelines: Generation and maintenance of GDS Study timelines with GDS and cross functional teams in MS Project Plan
Requirements:
High school diploma required
Preferred BA/BS degree with a focus in data science, statistics, computer science, life science, or related scientific discipline
MS Project, MS Office Suite (Word, PowerPoint, Excel) experience preferred
Concise, strong communication, verbal and written skills
Excellent organizational skills
What we offer:
Discretionary annual bonus
Discretionary stock-based long-term incentives
Paid time off
Company-sponsored medical, dental, vision, and life insurance plans