
Clinical Research Associate
2 weeks ago
Job Description:
We are seeking a highly skilled Clinical Research Associate (CRA) to join our team. As a CRA, you will be responsible for ensuring the quality and integrity of clinical trials by conducting on-site and remote monitoring, developing monitoring tools and procedures, and contributing to process design and delivery.
Responsibilities:
- Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.
- Develop and implement tools, procedures, and processes to ensure quality monitoring.
- Contribute to the design, implementation, and delivery of processes, programs, and policies.
- Manage defined components of projects or processes within the area of responsibility.
- Ensure accurate and timely documentation of monitoring activities and findings.
- Collaborate with cross-functional teams to support clinical trial operations.
Requirements:
- Bachelor's degree in a related field or equivalent experience.
- Minimum of 2-4 years of experience in clinical research monitoring.
- Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Excellent communication and interpersonal skills.
- Ability to work independently and manage multiple priorities.
- Proficiency in using clinical trial management systems and other relevant software.
Benefits:
- Opportunity to work in a dynamic and growing organization.
- Chance to contribute to the development of innovative solutions in clinical research.
- Collaborative and supportive work environment.
Others:
This is an exciting opportunity for individuals who are passionate about clinical research and want to make a meaningful contribution to the industry.
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