Research Program Coordinator I - Cardiology

Mount Sinai; United States; On-site; USD 60,000 - 90,000; Full time

Job summary

Mount Sinai is seeking a Research Program Coordinator I to develop and participate in study protocols, design management and statistical plans, analyze data and prepare final reports from study projects.

This role involves human subjects or laboratory research, collaboration with fellows, grant applications, budget development and regulatory compliance including IRB/IACUC processes. A strong foundation in natural sciences is required.

Qualifications

• Masters in Natural Sciences or Bachelors in Natural Sciences with 5 years of progressive research experience.
• 4–5 years of research experience in data management and study coordination in healthcare or basic research.

Responsibilities

• Provide consultation on research methodologies and statistical analysis issues.
• Participate in primary analysis of evaluation datasets.
• Design and implement research projects focusing on health outcomes.
• Assist in project design, sample size calculations and consulting on statistical analyses.
• Document and record observations per regulatory requirements and MSMC protocols.
• Supervise personnel and guide research methods and techniques.
• Assist the Principal Investigator or Research Manager on grant applications.
• Assist in developing budgets and grant proposals including pilot studies.
• Complete IRB/IACUC and other regulatory applications and renewals.
• Develop and amend protocols; write policies and procedures.
• Collaborate with fellows on research projects and papers for publication.

Skills

Research coordination

Statistical analysis

Grant applications

Data management

Education

Masters in Natural Sciences

Bachelors in Natural Sciences with 5 years of progressive research experience

Job description

The Research Program Coordinator I

The Research Program Coordinator I develops and/or participates in study protocols, designs management and statistical plans, analyzes data and prepares final reports from study. This position is responsible for human subjects or laboratory research, depending on department and type of study assigned.

1. Provides assistance and consultation on basic research or clinical trials methodologies and statistical analysis issues.
2. Participates in the primary analysis of evaluation datasets.
3. Designs and implements research projects focusing on health and interventions and their associated health outcomes.
4. Assists evaluation staff in project design, appropriate procedures and conduct and coordination by establishing sample size requirements, calculating issues associated with various evaluation design options and consulting on appropriate statistical analysis for proposed evaluations.
5. Documents and records observations on progress of research, investigations and data per regulatory requirements and MSMC protocols.
6. Supervises subordinate personnel and offers guidance on research methods and techniques.
7. Provides assistance to the Principle Investigator or Research Manager on grant applications.
8. Assists in the development of budgets for research projects. Completes grant applications and proposals by developing pilot studies and generating pre-clinical data.
9. Completes all Institutional Review Board (IRB) or IACUC and other regulatory applications and renewals.
10. Develops consent forms, screens and enrolls patients, follows patients through course of study, collects and analyze data. (Clinical Research only)
11. Develops policies and procedures within area of responsibility. Writes and amends protocols as necessary.
12. Participates in conferences, meetings and seminars concerning research and surveillance projects.
13. Collaborates with fellows on research projects and papers to be published.
14. Maintains and submits the regulatory requirements for the FREEDOM Clinical Coordinating Center at Mount Sinai Medical Center. (those performing Clinical Research only)
15. Performs other related duties.

Masters degree in Natural Sciences OR Bachelors degree in Natural Sciences plus 5 years of progressive research experience with some experience in research administration preferred 4 years of research experience (5 years if no Masters degree) in data management and study coordination in healthcare or basic research.