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Sr. Research Strategy & Program Specialist **Remote Available**
Company | Vanderbilt University Medical Center |
Address | Nashville, TN, United States |
Employment type | FULL_TIME |
Salary | |
Category | Hospitals and Health Care |
Expires | 2023-08-11 |
Posted at | 10 months ago |
Discover Vanderbilt University Medical Center: Located in Nashville, Tennessee, and operating at a global crossroads of teaching, discovery, and patient care, VUMC is a community of diverse individuals who come to work each day with the simple aim of changing the world. It is a place where your expertise will be valued, your knowledge expanded, and your abilities challenged. Vanderbilt Health recognizes that diversity is essential for excellence and innovation. We are committed to an inclusive environment where everyone has the chance to thrive and where your diversity of culture, thinking, learning, and leading is sought and celebrated. It is a place where employees know they are part of something that is bigger than themselves, take exceptional pride in their work and never settle for what was good enough yesterday. Vanderbilt’s mission is to advance health and wellness through preeminent programs in patient care, education, and research.
- Develop social media campaigns as well as graphic design and communications roles
- Act as a "go-to" resource for internal and external colleagues with less experience.
- Effectively lead/manage low- to mid-level institutional or national projects that have tight timelines and limited visibility.
- Educate the research community regarding resources available to clinicians and researchers to improve aspects of the research enterprise.
- Collaborate independently with internal and external customers to evaluate current services for continual improvement and develop new research tools.
- Provide independent, intermediate research support consultation and services, including regulatory, quality assurance and operational support, to all levels of research colleagues.
- Leads website development and support.
- The responsibilities listed are a general overview of the position and additional duties may be assigned.
- Lead programmatic efforts to locally produce videos, animated info graphics, and other educational materials.
- Play a lead role in the conduct of all tasks and activities required to complete projects and may oversee project activities of team members.
- Exhibit excellent interpersonal and communication skills in collaborating with internal and external customers.
- Collaborates with leaders on project planning and sets own objectives to deliver against responsibilities that have a direct impact on the near-term results of a low- to mid-level research project or program. Is familiar with key literature relevant to projects. Able to articulate how detailed tasks and assignments contribute to the broad goals of the organization.
- Demonstrates advanced knowledge in advising and assisting researchers and clinicians on improving the quality of research and grants by identifying collaborators, connecting investigators with resources/funding opportunities, and developing tools to further the research enterprise. Has played a lead role in identifying barriers to optimal study execution and formulate, implement, and assess solutions to those barriers. Independently identifies resources needed for the timely & successful completion of research projects. Provides available resources for preparing grant proposals, identifying study funding, ongoing financial management safety committees, IRB submissions, scientific review submission, study feasibility, recruitment methods, data management, and study implementation. May assist in the development of study budgets and billing grids to facilitate capture of all study costs and compliance with regulations. May assist in the development of reports, manuscripts, and other strategies for dissemination of research findings.
- Demonstrates comprehensive understanding of the optimal application of federal, state, and local laws, guidance documents, GCP/ICH guidelines, VUMC Institutional policies, and HRPP/IRB policies and procedures to meet the objectives of the VUMC and national research community. Has independently consulted on research and regulatory issues to identify solutions and develop improvement processes. Comprehends, manages, and facilitates IRB regulatory assurance(s), contracts, agreements, and IRB policies and procedures when appropriate. Tracks the progress of clinical research protocols through each step of the regulatory/administrative process and follows up as necessary to ensure efficient service when needed. Oversees coordination of ongoing analysis and modification of protocols and recommends amendments to study protocols, as appropriate. Assures adherence to FDA and other regulatory guidelines.
- Demonstrates proficiency in critically analyzing current research practices and policies through observation, data collection, peer reviews, literature reviews, interviews, and industry analysis to assess quality of existing workflow processes and identify improvements needed to maximize quality and efficiency. Able to independently develop and implement training programs on the strategic application of IRB policies and procedures, federal mandates and guidelines, GCP/ICH guidance, and other applicable topics (e.g., budget development, research billing, grants, contracts, COI). Independently provides ongoing consultation and education to research personnel regarding quality assurance.
- Demonstrates proficiency in providing guidance on operational goals, business strategies, ethical considerations, regulatory mandates, and institutional practices, policies and workflow. Has assisted investigators, key study personnel, and other team members in the development of data tools, record keeping, study budgets, process improvement plans, and efficient timelines for research studies. Advises on the development, implementation, and maintenance of comprehensive electronic systems including reporting to sustain efficient operations.
- Demonstrates advanced knowledge in broadening the institutional and national research community’s exposure to available digital tools and products. Has provided consultation, training, education, and assistance on use of digital services. Collaborates with technical professionals to inform the build, maintenance, and enhancement of electronic platforms and systems to support the needs of clinical researchers and projects, as well as objectives of the research enterprise. Serves a key role in developing content and designing usability and accessibility to determine user experience.
- Bachelor’s degree or equivalent experience (required)
- 3 years relevant experience (required)
- *Excellent organizational skills
- *Proven expertise in website development
- *Excellent oral communication skills
- *Excellent interpersonal skills
- *Excellent critical thinking skills
- *Proven expertise in writing and social media campaign development
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