Responsibilities: - Collect enter and manage clinical trial data using electronic data capture (EDC) systems.
- Perform data validation and query management to ensure data quality and compliance with study protocols.
- Assist in the development of case report forms (CRFs) and data management plans (DMPs).
- Conduct ongoing data review and discrepancy resolution in collaboration with clinical staff.
- Generate data listings and summaries for interim and final study reports.
- Ensure data handling is following GCP ICH guidelines and applicable regulatory requirements.
- Maintain study documentation audit trails and data queries logs.
- Participate in cross-functional study team meetings and contribute to project timelines.
Requirements: - Bachelors degree in life sciences healthcare information technology or related field.
- 1 3 years of experience in clinical data management or a related clinical research role.
- Familiarity with EDC systems (e.g. Medidata Rave Oracle Clinical Redcap).
- Knowledge of GCP ICH and regulatory guidelines.
- Excellent attention to detail organizational and communication skills.
- Proficiency in Microsoft Excel and other data management tools.
Responsibilities: Collect enter and manage clinical trial data using electronic data capture (EDC) systems. Perform data validation and query management to ensure data quality and compliance with study protocols. Assist in the development of case report forms (CRFs) and data management plans (DMPs)...
Responsibilities: - Collect enter and manage clinical trial data using electronic data capture (EDC) systems.
- Perform data validation and query management to ensure data quality and compliance with study protocols.
- Assist in the development of case report forms (CRFs) and data management plans (DMPs).
- Conduct ongoing data review and discrepancy resolution in collaboration with clinical staff.
- Generate data listings and summaries for interim and final study reports.
- Ensure data handling is following GCP ICH guidelines and applicable regulatory requirements.
- Maintain study documentation audit trails and data queries logs.
- Participate in cross-functional study team meetings and contribute to project timelines.
Requirements: - Bachelors degree in life sciences healthcare information technology or related field.
- 1 3 years of experience in clinical data management or a related clinical research role.
- Familiarity with EDC systems (e.g. Medidata Rave Oracle Clinical Redcap).
- Knowledge of GCP ICH and regulatory guidelines.
- Excellent attention to detail organizational and communication skills.
- Proficiency in Microsoft Excel and other data management tools.
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