Responsibilities: - Develop and implement data management plans for clinical trials.
- Ensure data quality and integrity throughout the trial.
- Develop and maintain study-specific data management documents such as data management plans annotated CRFs and database specifications.
- Collaborate with cross-functional teams to identify project priorities and timelines.
- Manage data quality assurance procedures and perform quality control checks.
- Ensure adherence to regulatory compliance by following relevant guidelines and standard procedures.
- Contribute to the development of standard operating procedures (SOPs) and work instructions.
- Prepare and review database validation and user acceptance testing.
- Perform database lock activities including data reconciliation and database closure.
Requirements: - Bachelors degree in a relevant field such as life sciences or a related discipline.
- Freshers in clinical data management of drug development programs.
- Familiarity with regulatory guidelines such as ICH/GCP and FDA regulations.
- Strong analytical and problem-solving skills.
- Excellent attention to detail and organization skills.
- Good interpersonal and communication skills to work effectively in a team environment.
Responsibilities: Develop and implement data management plans for clinical trials. Ensure data quality and integrity throughout the trial. Develop and maintain study-specific data management documents such as data management plans annotated CRFs and database specifications. Collaborate with cross-f...
Responsibilities: - Develop and implement data management plans for clinical trials.
- Ensure data quality and integrity throughout the trial.
- Develop and maintain study-specific data management documents such as data management plans annotated CRFs and database specifications.
- Collaborate with cross-functional teams to identify project priorities and timelines.
- Manage data quality assurance procedures and perform quality control checks.
- Ensure adherence to regulatory compliance by following relevant guidelines and standard procedures.
- Contribute to the development of standard operating procedures (SOPs) and work instructions.
- Prepare and review database validation and user acceptance testing.
- Perform database lock activities including data reconciliation and database closure.
Requirements: - Bachelors degree in a relevant field such as life sciences or a related discipline.
- Freshers in clinical data management of drug development programs.
- Familiarity with regulatory guidelines such as ICH/GCP and FDA regulations.
- Strong analytical and problem-solving skills.
- Excellent attention to detail and organization skills.
- Good interpersonal and communication skills to work effectively in a team environment.
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