Senior Research Coordinator Jobs

Atria Physician Practice New York PC is seeking a highly motivated and detail-oriented Senior Research Coordinator to join our team. As the Senior Research Coordinator, you will be responsible for supporting the clinical research programs across our organization, contributing to the development of cutting-edge medical care. Atria is revolutionizing the medical industry by using the latest science to provide patients with personalized preventive care. Our team is focused on proactive and preventive healthcare, with a mission to improve the quality of life for individuals globally. By joining Atria, you will become part of a team dedicated to changing the world and improving the lives of patients.

Responsibilities

• Creates, maintains, and updates the designated database for each research protocol
• Builds and maintains a broad network of professional relationships with participants, principal investigator, co‐investigators, research study staff, and other collaborators to ensure successful research collaborations
• Develop, implement, and coordinate the research-related activities
• Plans and coordinates all aspects of multiple research projects
• Participates with a team in the development and authoring of research protocols
• Collaborate with interdisciplinary teams and experts to conduct clinical trials
• Oversee and manage clinical research projects and studies from initiation to completion
• Ensure compliance with regulatory requirements and guidelines
• Maintains inventory of supplies or equipment, prepares study kits and requisitions prior to study visits to ensure the appropriate items are available when necessary
• Manage and oversee data collection and analysis
• Assists with writing abstracts and manuscripts
• Identifies and reports issues that may affect the accuracy and quality of study design and implementation to meet study aims
• Participates in internal/external research related meetings and investigator meetings to build and maintain relationships.
• Prepare and submit research protocols, manuscripts, and applications for grants
• Interpret complex data sets and provide clear summaries for presentations or scientific publications
• Prepares and maintains all IRB and regulatory paperwork to comply with institutional regulatory requirements
• Adheres to ethical standards
• Abstracts or collects data from study subjects and enters information into the designated forms/database to comply with study protocols
• Assists the clinical research team in the implementation of research studies to ensure successful completion of study goals

Salary Range: $75,000 - $90,000

Requirements

• Strong organizational skills with attention to detail
• Excellent communication and interpersonal skills
• Proficiency in Microsoft Office is required.
• At least 3 years of experience in clinical research, including experience with clinical trials, required
• Knowledgeable of FDA regulations and guidelines
• Ability to work independently and as part of a team
• Experience in research protocol development and grant writing is preferred
• Bachelor's degree in a healthcare-related field or equivalent experience required

Benefits

At Atria, we are proud to offer every member of the Atria team:

• Time to give back and make an impact in underserved communities
• Clinic Family Days that are scheduled throughout the year so your family may share the wealth of our clinician expertise and state-of-the-art technology services
• Excellent health and wellness benefits, 100% paid by Atria