A Study Management Associate (SMA) is typically a role within the field of clinical research or pharmaceutical industry. The primary responsibility of a Study Management Associate is to provide support to the study management team in planning, executing, and monitoring clinical trials or research studies. Their tasks may vary depending on the organization and specific study, but generally, their responsibilities include:
Study Planning: SMAs assist in the development and implementation of study protocols, study manuals, and study-specific procedures. They contribute to the design of data collection tools and ensure they comply with regulatory requirements.
Regulatory Compliance: SMAs help ensure that all necessary regulatory documentation and approvals are obtained before the study can commence. They may assist with submitting study protocols and other required documents to regulatory authorities and ethics committees.
Study Execution: During the course of the study, SMAs support the study management team by coordinating various activities. They may assist in site selection and initiation, preparing study-related materials, organizing investigator meetings, and providing training to study site personnel.
Data Management: SMAs play a role in data collection and management. They may assist in setting up electronic data capture systems, monitoring data quality, and resolving data discrepancies. They may also contribute to the development of data management plans.
Study Monitoring: SMAs may participate in monitoring visits to study sites to ensure adherence to the study protocol, regulatory guidelines, and good clinical practices. They may assist in reviewing source documents, verifying data accuracy, and resolving any issues identified during monitoring.
Documentation and Reporting: SMAs help maintain study documentation and ensure it is complete and accurate. They may assist in the preparation of study reports, including interim and final reports, and contribute to study publications or presentations.
Communication and Collaboration: SMAs collaborate with various stakeholders involved in the study, including study sponsors, investigators, study site personnel, and other study team members. They may assist in facilitating communication, organizing meetings, and maintaining effective working relationships.
Study Management Associates provide essential support to ensure the smooth execution of clinical trials or research studies, assisting in various aspects of study planning, execution, data management, and regulatory compliance.
Here is an overview of Cincinnati and its potential as a life sciences location:
Home to several large healthcare systems including Cincinnati Children's Hospital Medical Center, TriHealth, Mercy Health, and UC Health. This provides clinical research and talent pipelines.
The University of Cincinnati and Cincinnati State Technical and Community College offer relevant life sciences degree programs.
Multiple business parks and incubators exist, like Hamilton Landing and BioStart, aimed at attracting biotech companies.
Several large companies have presences, including Procter & Gamble, Kroger, and Ethicon Endo-Surgery. Opportunities for partnerships.
Part of a tri-state region with Northern Kentucky and Indianapolis, providing access to a large labor pool.
Cost of living and real estate are lower compared to major biotech hubs.
However, lacks the density of other emerging biotech hubs like Miami or San Diego. Early stages of development.
Ohio provides some tax incentives but less VC funding compared to coastal states.
Cincinnati offers affordable real estate, clinical assets, and a skilled workforce that could support growth of its life sciences sector.