Clinical Trials Coordinator - Data & Compliance Focus

Touro University; Town of Mount Pleasant (NY); On-site; USD 43,680 - 54,600; Full time

Job summary

New York Medical College is seeking a clinical research coordinator to join the Division of Medical Genetics on multiple trials. The candidate will bring up to two years of trial experience, with training available.

Responsibilities include protocol review, regulatory submissions, data entry, and coordinating drug supply and budget/BUDIR reviews. The role is full-time and grant-supported, contingent on funding, with a salary range listed publicly.

Qualifications

• Bachelor's degree required, preferably in health‑science field.
• Proficiency with Microsoft Office suite, including Word, Excel, and Outlook.
• Must be adept at keeping track of multiple projects, able to work independently, and have strong problem solving, communication, and analytical skills.

Responsibilities

• Review and analysis of clinical trial protocols and informed consent forms.
• Assist Principal and Sub-Investigator in study start-up process.
• Coordinate budget review and IRB reviews.
• Submission of regulatory documents and communication with IRB.
• Data entry, management of queries.
• Managing supply of investigational study drug with temperature monitoring.
• Invoicing Study Sponsor for study procedures as per contract requirements.
• Coordinating transportation and lodging with submission of patient travel and meal receipts to Sponsor.
• Management of medical supplies and related product orders.
• Packing and shipping of clinical laboratory specimens.
• Maintain source documents in accordance with FDA and GCP guidelines.
• Other duties as assigned.

Skills

Project tracking

Independent work

Problem solving

Communication

Analytical thinking

Education

Bachelors degree

Tools

Microsoft Office

Job description

Overview

The Division of Medical Genetics at New York Medical College is seeking a clinical research coordinator to work with our team on multiple clinical trials. The ideal candidate has 2 years of clinical trial experience, but we are willing to train the right candidate. The coordinator will be working on investigational drug studies as well as prospective and retrospective data entry for multiple studies.

Overview

The Division of Medical Genetics at New York Medical College is seeking a clinical research coordinator to work with our team on multiple clinical trials. The ideal candidate has 2 years of clinical trial experience, but we are willing to train the right candidate. The coordinator will be working on investigational drug studies as well as prospective and retrospective data entry for multiple studies.

Category: Full-time, Grant Supported Position-(Position is contingent on continued funding)

Responsibilities

• Review and analysis of clinical trial protocols and informed consent forms
• Assist Principal and Sub-Investigator in study start-up process
• Coordinate budget review and IRB reviews
• Submission of regulatory documents and communication with IRB
• Data entry, management of queries
• Managing supply of investigational study drug with temperature monitoring
• Invoicing Study Sponsor for study procedures as per contract requirements.
• Coordinating transportation and lodging (as needed) with submission of patient travel and meal receipts to Sponsor
• Management of medical supplies and related product orders
• Packing and shipping of clinical laboratory specimens
• Maintain source documents in accordance with FDA and GCP guidelines
• Other duties as assigned
  
  

Qualifications

• Bachelor's degree required, preferably in health-science field
• Proficiency with Microsoft Office suite, including Word, Excel, and Outlook
• Must be adept at keeping track of multiple projects, able to work independently, and have strong problem solving, communication, and analytical skills
  
  

Minimum Salary

USD $43,680.00/Yr.

Maximum Salary

USD $54,600.00/Yr.