Alzheimer's Disease Prevention Coordinator

4 days ago


SaintBauzilledePutois, Occitanie, United States The Roskamp Institute, Inc Full time
Make a Difference
Clinical Research Coordinator for Alzheimer's Disease Prevention and Environmental Health Studies
The Roskamp Institute, Inc is seeking an experienced Clinical Research Coordinator to support our groundbreaking studies in Alzheimer's disease prevention and environmental health. As a member of our team, you will be at the forefront of these critical research initiatives, working directly with patients, physicians, and research teams to ensure the success of these vital research projects.

**About the Role**
We are looking for a highly motivated and organized individual to join our team as a Clinical Research Coordinator. The successful candidate will have a strong understanding of clinical research protocols and regulatory requirements, excellent organizational, communication, and interpersonal skills, and the ability to work independently and as part of a collaborative team. The ideal candidate will also have experience in phlebotomy and a strong commitment to patient safety and study integrity.

**Responsibilities**
- Coordinate all aspects of the PACT and Red Tide studies, ensuring adherence to study protocols and regulatory guidelines.
- Collaborate with research teams, physicians, and participants to facilitate the safe and effective conduct of clinical trials.
- Manage patient recruitment, screening, enrollment, and follow-up processes.
- Perform clinical assessments and monitor patient progress throughout the study.
- Collect, process, and manage laboratory samples, including blood draws (phlebotomy).
- Maintain accurate and detailed study documentation, case report forms (CRFs), and ensure regulatory compliance.
- Ensure compliance with Good Clinical Practice (GCP) and relevant safety regulations.

**Requirements**
- Experience as a Clinical Research Coordinator or in a similar clinical research environment.
- Phlebotomy skills (Required) – Proficiency in performing blood draws, sample collection, and processing.
- Preferred: Registered Nurse (RN) or Licensed Practical Nurse (LPN) with clinical experience.
- Strong understanding of clinical research protocols and regulatory requirements.
- Excellent organizational, communication, and interpersonal skills.
- Ability to work independently and as part of a collaborative team.

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