RWE Site Coordinator
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Job Location:
Manchester, CT - USA
Monthly Salary:
Not Disclosed
Posted on:
7 hours ago
Vacancies:
1 Vacancy
Job Summary
We are seeking an experienced Real-World Evidence (RWE) Site Coordinator to lead the execution and delivery of critical research initiatives that will shape the future of infusion device this high-impact role you will serve as the central hub connecting product teams clinical sites and research stakeholders to design and implement comprehensive evaluation protocols across regional and global sites. Youll take ownership of the entire research lifecyclefrom developing data collection strategies and managing KPI integrity to analyzing results and driving publication-ready insights. This position offers the opportunity to provide strategic thought leadership while working hands-on with cutting-edge clinical systems and EMR platforms to advance real-world evidence in healthcare delivery.
How you will make an impact as a RWE Site Coordinator:
One hour from the beach Boston and the mountains the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research and Development where we are taking the same innovation and cutting-edge technology into the modern age.
Behind DEKAs brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering design and manufacturing. Here at DEKA some of the most innovative and life-changing products of our time are created and new ideas are always welcome and explored.
How you will make an impact as a RWE Site Coordinator:
- Lead end-to-end research execution and delivery for regional or global research initiatives
- Partner with product operations and clinical teams to ensure alignment on priorities and timelines
- Work with all parties (Site Site lead Steering Committee Training Team and Clinical team) to develop a comprehensive evaluation plan and/or evaluation protocol(s)
- Manage day to day responsibilities for collection of study/evaluation-critical data from use of the infusion devices qualitative and quantitative.
- Lead the development of the identification and collection of KPIs related to the RWE to ensure integrity for later analysis and publication.
- This includes:
- the selection of an appropriate data collection platform
- the appropriate tools for collection or input of the data
- the oversight of any personnel (employees or contracted entities) involved in the data collection analysis and/or write-up/summary
- Summarize critical data from studies summarize in written form and present appropriate results in a logical and compelling fashion.
- Provide outreach tracking and follow-up with new or potential RWE sites in the US or OUS to fulfill additional research or evaluation requirements.
- Provide internal thought leadership on and collaboration with risk and ethics committees to review study feasibility site capability and safety monitoring processes.
- Demonstrate competence in study development including strategy execution data collection and security data analysis study write-up and publication acceptance. RN preferred but not necessary. Knowledge of medical device industry preferred with knowledge and success in research in clinical environment a must.
- Degree Requirements: BS or BSN with preference for any advanced degree of relevance to professional competency.
- Clinical Systems & Platform / EMR/EHR Experience including:
- Epic
- Cerner
- Meditech
- Allscripts
- Experience leading direct day-to-day clinical operations across multiple national research sites
- Experience managing inpatient and outpatient evaluations for various therapies devices and/or case use studies.
- Demonstrate a proven ability to summarize critical data from studies summarize in written form and present appropriate results in a logical and compelling fashion.
- Evidence of clinical publication success is a plus.
- Proficient with Microsoft Office Suite
- Motivated energetic and a self-starter
- Required travel requirements: 25-50% travel. Local (Office) and Clinical site requirements.
- Phase 1: Manchester NH
- Phase 2: Cleveland OH
One hour from the beach Boston and the mountains the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research and Development where we are taking the same innovation and cutting-edge technology into the modern age.
Behind DEKAs brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering design and manufacturing. Here at DEKA some of the most innovative and life-changing products of our time are created and new ideas are always welcome and explored.
Required Experience:
Senior IC
Key Skills
- Experience Working With Students
- Google Docs
- Organizational skills
- Classroom Experience
- Data Collection
- Materials Handling
- Workers' Compensation Law
- OSHA
- Special Operations
- Team Management
- Experience with Children
- Supervising Experience
About Company
DEKA Research and Development is perhaps best known for its founder and president Dean Kamen -- and for the Segway Personal Transporter he invented. DEKA is a design and engineering firm that develops innovative technologies, many of them in the field of medical devices. The Segway it ... View more
