Clinical Research Associate I
6 days ago
Parexel is seeking a highly skilled Clinical Research Associate I to join our team. As a Clinical Research Associate I, you will be responsible for managing clinical sites, ensuring compliance with regulatory requirements, and executing study protocols.
Key Responsibilities- Site Management
- Build and maintain relationships with investigators and site staff
- Conduct site qualification and initiation visits
- Manage site-specific documentation and regulatory submissions
- Ensure site compliance with study protocols and regulatory requirements
- Study Execution
- Develop and implement study plans and strategies
- Manage site-level data and ensure data quality and integrity
- Conduct remote visits and contacts as needed
- Generate visit/contact reports and ensure timely submission
- Regulatory Compliance
- Ensure compliance with ICH-GCP and applicable international and local regulations
- Monitor and maintain regulatory documentation and submissions
- Collaborate with cross-functional teams to ensure regulatory compliance
- Education
- Degree in biological science, pharmacy, or other health-related discipline preferred
- Experience
- Previous relevant work experience preferred
- Skills
- Problem-solving skills
- Able to work independently and as part of a team
- Strong communication and interpersonal skills
- Ability to manage multiple tasks and prioritize
Parexel is a leading global biopharmaceutical services company. We provide a comprehensive range of services to help our clients succeed in the development and delivery of innovative therapies.
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