Clinical Trials Data & Protocol Manager

Mount Sinai Morningside; New York (NY); On-site; USD 59,000 - 89,000; Full time

Job summary

Mount Sinai Morningside is seeking a professional to supervise and coordinate data collection, entry, and retrieval for the department. The role involves protocol development, regulatory oversight, and data management across all phases of clinical trials in a dynamic research environment.

The candidate will support IRB submissions, study feasibility, and collaboration with investigators and study teams to ensure accurate data capture and reporting for regulatory filings and research outcomes.

Qualifications

• HS Diploma required.

Responsibilities

• Coordinate protocol development activities with investigators across all phases.
• Develop investigator-initiated projects and coordinate study development.
• Coordinate and communicate with investigators and team to aid in study oversight throughout the life-cycle of clinical trials.
• Regulatory activities: oversee regulatory processes for projects and prepare IRB submissions.
• Data Management/Analysis: create, manage, protect departmental research systems, organize, store, and analyze data.
• Data entry and maintenance; create databases and perform data acquisition/mining.
• Track and report study progress; maintain regulatory documents and study status.

Skills

Data management

Data analysis

Regulatory knowledge

Education

HS Diploma

Tools

SPSS

REDCap

SAS

R

Job description

Mount Sinai Morningside is seeking a professional to supervise and coordinate data collection, entry, and retrieval for the department. The role involves protocol development, regulatory oversight, and data management across all phases of clinical trials in a dynamic research environment.

The candidate will support IRB submissions, study feasibility, and collaboration with investigators and study teams to ensure accurate data capture and reporting for regulatory filings and research outcomes.