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Everest Clinical Research

Clinical Data Manager I

1w

Everest Clinical Research

Taipei, TW · Full-time · TWD 900,000 – TWD 1,500,000

About this role

Everest Clinical Research is a full-service contract research organization providing clinical research services to pharmaceutical, biotechnology, and medical device industries. With headquarters in Markham, Ontario, and offices in Taipei, Taiwan, Everest excels in high-quality deliverables and customer service. Join our dynamic team as a Clinical Data Manager I for the Taipei office, on-site.

Plan, manage, control, and perform data processing activities for assigned projects in timely, accurate compliance with sponsors' requirements. Lead data management projects applying project management skills and techniques while coordinating timelines. Specify database validation checks and develop standards for common and therapeutic-specific modules.

Define and monitor clinical trial dataflow and quality control processes per SOPs and guidelines. Design and review patient Case Report Forms, test data entry screens, and validate captured data. Perform QC procedures on databases during trials and at closure.

Train and supervise data entry and junior personnel on study procedures and data handling. Validate study progress reports and assist in resolving data coding discrepancies. Contribute to Everest's growth with quality as backbone, customer-focus as tradition, and flexibility as strength.

Requirements

  • Bachelor's degree in health and/or pharmaceutical sciences, physical/biological sciences
  • Project management skills for clinical data processing projects
  • Knowledge of database validation checks and standards
  • Experience defining clinical trial dataflow and QC processes
  • Proficiency in CRF design, database schema, and data entry screen testing
  • Skills in data validation, query writing, and discrepancy resolution
  • Ability to perform database QC and closure checks
  • Experience training data management personnel on study procedures

Responsibilities

  • Plan, manage, control, and perform data processing and management activities for assigned projects
  • Lead assigned data processing and management projects by applying project management skills
  • Specify database validation checks for assigned studies and develop standard checks
  • Define and monitor clinical trial dataflow and quality control processes per SOPs
  • Design and review patient Case Report Forms and database schema
  • Validate electronically captured data and write queries on discrepancies
  • Perform QC procedures on databases during trials and at study closure
  • Train and supervise data entry and junior data management personnel