Clinical Research Coordinator

New York Medical College • Town of Mount Pleasant, NY

4d

About The Position

The candidate will report to Dr. Salomon Amar, VP for Research, and to Dr. Islam, Chair of PMI. The incumbent will manage all aspects of the research study. Attention to detail, self-starter, organized as well as good communication skills. Applicant must adhere to patient confidentially as well as oversees various studies effectively and efficiently.

Requirements

• Bachelor's degree in biology, mathematics, computer science, natural sciences, or related areas.
• Minimum of two years of related professional experience
• Phlebotomy training and/or certification required.
• Ability to use a combination of validated Electronic Data Capture (EDC) systems and/or other internal or commercial software tools and proven ability to learn and apply new software quickly as projects require
• Strong IT skills, including excellent knowledge of various software programs and packages including MS Word, Excel
• Ability to work effectively both as part of a project team and independently is essential
• Excellent oral and written English communication skills.
• Proven experience using data management systems, tools and processes to support multi-site, multi-mode research studies.
• Ability to effectively apply knowledge and skills in a highly organized fashion while adhering to required guidelines, SOPs and client expectations.
• Good organizational and analytical/problem-solving skills with strong attention to detail.
• Ability to work productively with minimal supervision.
• Ability to attain, maintain and apply a working knowledge of GCPs and applicable SOPs.
• Strong patient focus and excellent interpersonal skills.

Nice To Haves

• CITI certified preferred (but can be trained at NYMC).

Responsibilities

• Contribute to the development and implementation of SOPs, project-specific procedures, budgets, and technical guidance documents.
• Monitor, adherence to protocols.
• Establish data and workflow plans.
• Designing IRB consent forms for the project.
• Identify and enroll patients at study sites.
• Obtain, track, and administer all patient and specimen data in TissueMetrix2 Redcap database or other databases.
• Perform QC review of data and coordinating timely corrections to the database with the PI.
• Interface with investigational sites, clinical consultants, and lab.
• Direct all aspects of clinical trial data generation and analysis including external site clinical studies and internal analytical studies.
• Monitoring study performance metrics using standard study management tools.
• Drive internal communication, including timelines, budget, progress, and project needs.
• Manage budgets.
• Pick up/Deliver specimens as needed
• Other duties as needed.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 501-1,000 employees