Senior Clinical Research Coordinator & Protocols Lead

Mount Sinai Morningside; New York (NY); On-site; USD 72,881 - 116,693; Full time

Job summary

Mount Sinai Morningside is seeking a clinical research professional to generate and interpret highly complex data, develop protocols, and mentor junior staff. You will oversee study subject assessments, data handling, and budget-related tasks while ensuring regulatory and protocol compliance across sites.

The role involves coordinating with investigators and regulatory teams, preparing grant and IRB documents, and contributing to research reporting for conferences.

Qualifications

• Bachelor's degree in sciences or related field.
• Master's degree preferred.
• 5 years of clinical research.

Responsibilities

• Generates highly complex data gathered on clinical research studies.
• Interprets complex clinical research data.
• Conducts clinical testing, develops protocols and assures all protocol procedures are approved.
• Prepares reports for presentation in conferences and seminars.
• Mentors, trains and reviews the work of less experienced clinical research staff.
• Develops workflow policies and procedures, prepares manuals and documents related to operations of the function.
• Oversees the clinical assessments of the study subjects including screening, evaluation and testing.
• Oversees data collection, processing, storage, inventory and quality control for clinical research studies.
• Assists in budget preparation and negotiation.
• May prepare and ensure grant applications, IRB / GCO documents are submitted.
• Coordinates protocols and human subject approvals between various sites.
• Assists the Principal Investigator and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials.
• May obtain informed consent under general supervision of the Investigator(s) and educate participants regarding study requirements
• Performs other related duties.

Education

Bachelor's degree in sciences or related field

Master's degree preferred

Job description

Mount Sinai Morningside is seeking a clinical research professional to generate and interpret highly complex data, develop protocols, and mentor junior staff. You will oversee study subject assessments, data handling, and budget-related tasks while ensuring regulatory and protocol compliance across sites.

The role involves coordinating with investigators and regulatory teams, preparing grant and IRB documents, and contributing to research reporting for conferences.