Clinical Research Coordinator: Trials and Data Management

Touro College; 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

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