Responsibilities
Clinical Research Associate Job Description
- Pre-Trial:
- Identify and qualify potential clinical trial sites and investigators.
- Set up and equip trial sites with necessary materials and equipment.
- Train site staff on study procedures and data collection methods.
- Develop and maintain study manuals and documentation.
- Monitoring:
- Conduct regular visits to trial sites to monitor progress and adherence to protocols.
- Review case report forms and other data for accuracy and completeness.
- Identify and address any safety concerns or protocol deviations.
- Report significant findings and updates to sponsors and regulatory authorities.
- Post-Trial:
- Assist with data analysis and study close-out activities.
- Prepare final study reports and presentations.
- Contribute to the regulatory submission process.
Additional Responsibilities May Include
- Managing study budgets and timelines.
- Liaising with ethics committees and regulatory agencies.
- Providing scientific and technical support to study teams.
- Participating in training and development programs.
Qualifications
- 0- 2 years’ experience
- Bachelor’s degree in life sciences,nursing,or a related field.
- Master’s degree preferred,especially for senior positions.
- Good understanding of Good Clinical Practice guidelines and regulations.
- Excellent communication,interpersonal,and organizational skills.
- Strong attention to detail and ability to multitask.
- Ability to travel frequently and independently.