Medical Monitor Professional
4 days ago
The Role
IQVIA Argentina is seeking a Medical Monitor Professional to join our team. The ideal candidate will have experience in clinical research and be able to monitor clinical studies effectively.
Key Responsibilities
- Monitor clinical sites to ensure compliance with Good Clinical Practice (GCP).
- Collaborate with sites to develop and track subject recruitment plans to enhance predictability.
- Provide protocol and related study training to assigned sites and maintain regular communication.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
- Monitor study progress by tracking regulatory submissions, case report form completion, data query generation, and resolution.
- Maintain accurate records of site management, monitoring visit findings, and action plans.
- Collaborate with study team members for project execution support as needed.
Requirements
- Bachelor's degree in a scientific discipline or healthcare preferred.
- At least 2 years of on-site monitoring experience.
- Excellent knowledge of clinical research regulatory requirements, GCP, and ICH guidelines.
- Strong analytical and problem-solving skills.
- Excellent communication and interpersonal skills.
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