Project Coordinator - Research, HVC - Dartmouth-Hitchcock Health

Conducts Heart and Vascular focused research on multiple projects and works with others in the research group to develop the research approach and design and also executes deliverables in support of these projects. May contribute to writing related papers and grant proposals in support of research activities. May work on projects with grant funding and clinical trial schedules and responsibilities, as well as a variety of process improvement and administrative duties.

1. Serves as major contributing member to the research program, participating in the development of the research hypothesis and planning the project parameters and scope.
2. Independently conducts research on aspects of multiple projects and provides leadership to others participating in the project.
3. Collects, analyzes and interprets data resulting from projects and presents findings and their significance in various settings such as lab meetings, conferences, and may author or co-author research findings and present at national conferences.
4. May find/obtain funding for research projects and write grant proposals and applications.
5. May hire, supervise, train, and evaluate staff and student assistants to meet changing department needs.
6. Oversees general laboratory operations to ensure proper methods, procedures and techniques and provides technical guidance and direction. Advises on the need for and type of equipment and supply purchase, use, maintenance, and availability.
7. Performs other duties as required or assigned.

• Bachelor’s Degree in applicable field of study with five (5) years of research experience or the equivalent in education and experience required.
• Master’s Degree or PhD or foreign equivalent in relevant field, preferred.
• Comprehensive knowledge of laboratory and research methods, procedures, and techniques as well as equipment and instruments.
• Depending on the assigned area, experience in animal models or a strong background with human research will be necessary.
• A scientific background in an environmental, chemical or biological field preferred.
• Prior experience with IRB, regulatory oversight of clinical trials and knowledge of Good Clinical Practice (GCP) preferred.
• Willingness to be exposed to and work with hazardous and or infectious materials and/or hazardous chemicals.
• Exceptional organizational and management skills to plan and organize the research approach and project parameters.
• Ability to work independently and apply critical thinking and sound judgment.
• Ability to manage laboratory inventory and records.
• Excellent oral communication and interpersonal skills.
• Knowledge of computer software applications used for research investigations and data analysis and presentation as well as on line search engines.