Clinical Research Coordinator
Job Description
Job Description
MORE Foundation is a non-profit dedicated to Keeping Life in Motion through innovative research, community education and charitable assistance programs.
The Foundation conducts both laboratory based and clinical research in collaboration with physician groups and leading healthcare organizations such as The CORE Institute and HOPCo.
Our biomechanics lab is home to the most advanced robotic testing systems in the industry. Our Human Motion Laboratory uses advanced motion analysis techniques to measure the movement of the body after and after different treatment interventions.
MORE Foundation’s clinical research program conducts multiple clinical studies of orthopedic devices, pharmaceuticals and rehabilitation protocols each year to help advance the standard of patient care.
Our programs are staffed with clinicians, clinical research specialists, bioengineers and scientists who are truly dedicated to our mission.
MORE Foundation is accredited by ArMA as a provider of medical education (CME) and we work with multiple societies and entities to review and accredit educational courses.
Our charitable assistance programs deliver free prosthetic hands to children who are not able to obtain prosthetics through traditional care pathways and provide free rides to military veterans that are unable to reach medical appointments without assistance.
MORE Foundation provides a dynamic working environment with hands-on interaction with patients, clinicians, scientists and technologies from a diverse array of backgrounds to provide opportunities for personal and professional growth.
We are looking for a Clinical Research Coordinator to join our growing team. See below for functions and requirements for this position.
Benefits :
- Salary $22-26 / hr DOE
- Competitive Health & Welfare Benefits
- Monthly $43 stipend to use toward ancillary benefits
- HSA with qualifying HDHP plans with company match
- 401k plan after 6 months of service with company match (Part-time employees included)
- Employee Assistance Program that is available 24 / 7 to provide support
- Employee Appreciation Days
- Employee Wellness Events
ESSENTIAL FUNCTIONS
- Review potential protocols to evaluate their feasibility and advise on implementation within standard clinical practices
- Recruits study participants by referrals from clinical sites; schedules appointments, and interviews and evaluates potential participants to ensure they meet eligibility requirements;
instructs participants concerning protocol and obtains informed consent.
- Monitors and participates in research activities including data collection, data entry, and analysis for a research project.
- Schedules and / or coordinates the scheduling of required laboratory tests and / or radiographic exams
- Assists in developing patient educational materials and provides patient and / or family members with instructions on investigational drug / device administration and other pertinent information related to study participation.
- Assists in preparing forms for submission to appropriate oversight / regulatory committees
- Is the primary resource to clinical and support staff within the scope of the study; ensures adherence to clinical and imaging protocols, scheduling study visits within protocol windows, and appropriate sites of service for study activities.
- Prepares and submits study-related reports to sponsors, institutional review boards and other parties as required.
- Completes case report forms for study participants and documents applicable data in study records / databases.
- Inventories and requisitions research study supplies and equipment
- Conducts clinical research in compliance with all applicable SOPs, laws, and standards
EDUCATION
Associate Degree with two years of clinical trial experience or Bachelor's degree in a related medical field
EXPERIENCE
- Two plus years’ experience in the health care field or an equivalent combination of education and experience.
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