Senior Biostatistician managing statistical expertise for Arthrex's Research team in Munich. Overseeing study designs, compliance, and analytics to support medical device research.
About the role
- Clinical Research Coordinator managing significant aspects of clinical trials at Winship Cancer Institute. Fostering excellence in cancer research and treatment collaboration across disciplines.
Responsibilities
- Independently manages significant and key aspects of a large clinical trial or all aspects of one or more small trials, or research projects.
- Trains and provides guidance to less experienced staff.
- Oversees data management for research projects.
- Interfaces with research participants and resolves issues related to study protocols.
- Authorizes purchases for supplies and equipment maintenance.
- Determines effective strategies for promoting/recruiting research participants and retaining participants in long term clinical trials.
- Periodically audits operations including laboratory procedures to ensure compliance with applicable regulations; provides leadership in identifying and implementing corrective actions/processes.
- Monitors IRB submissions and responds to requests and questions.
- Interfaces with study sponsors, monitors and reports SAEs; resolves study queries.
- Provides leadership in determining, recommending, and implementing improvements to policies/processes.
- Assists in developing grant proposals and protocols.
- With appropriate credentialing and training may perform phlebotomy, specimens collection or diagnostics.
- May perform some supervisory duties.
- Performs related approved responsibilities as required.
Requirements
- High School Diploma or GED and seven years of clinical research experience.
- Two years of college in a scientific, health related or business administration program and five years of clinical research experience
- Licensed as a Practical Nurse (LPN) and four years of clinical research experience
- Bachelor's degree in a scientific, health related or business administration program and three years clinical research experience
- Master’s degree, MD or PhD in a scientific, health related or business administration program and one year of clinical research experience
- Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred.
Benefits
- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
- Professional development
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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