Multi-Sponsor CRA Role with Excellent Work-Life Balance
vor 1 Woche
Job Summary:
Meet is seeking a highly skilled Clinical Research Associate/CRA II to join our team in a homebased opportunity. As a CRA II, you will be responsible for performing clinical study site management/monitoring activities in compliance with ICH-GCP and Sponsor SOPs.
Key Responsibilities:
- Perform site initiation, monitoring, and close-out visits in accordance with ICH-GCP and Sponsor SOPs.
- Ensure compliance with regulatory documentation for study start-up, maintenance, and close-out.
- Develop and maintain strong relationships with site personnel and sponsors.
- Collaborate with cross-functional teams to ensure timely and successful study execution.
- Identify and report any site-related issues or concerns to the project team.
Requirements:
- Strong understanding of clinical research and regulatory requirements.
- Excellent communication and interpersonal skills.
- Ability to work independently and as part of a team.
- Strong problem-solving and analytical skills.
- Proficiency in Microsoft Office and clinical trial management systems.
What We Offer:
- Competitive salary and bonus structure.
- Opportunities for career growth and professional development.
- Flexible work arrangements, including homebased work options.
- Collaborative and dynamic work environment.
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