Clinical Research Coordinator

Talentify; Town of Mount Pleasant (NY); On-site; USD 44,000 - 55,000; Full time

Job summary

New York Medical College is seeking a clinical research coordinator to support multiple clinical trials within the Division of Medical Genetics. The role involves data entry, study start-up activities, regulatory submissions, and coordination with sponsors across investigational drug studies.

The ideal candidate has 2 years of clinical trial experience but we are willing to train the right candidate. A bachelor’s degree is required, and strong organizational and communication skills are

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 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

MS Office

Multi-project management

Communication skills

Analytical skills

Education

Bachelor's degree

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.

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.