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New York Medical College · 10 hours ago

Clinical Research Coordinator

US-NY-Valhalla

Full-time

Onsite

Entry, Mid Level

$36K/yr - $45K/yr

2+ years exp

New York Medical College is seeking a Clinical Research Coordinator to manage all aspects of research studies. The role involves developing SOPs, monitoring protocol adherence, managing budgets, and ensuring effective communication with various stakeholders.

BiometricsMedicalUniversities

Work & Life Balance

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

Qualification

CITI certificationPhlebotomy trainingData management systemsElectronic Data Capture (EDC)MS WordExcelAnalytical skillsCommunication skillsOrganizational skillsTeamworkAttention to detail

Required

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