Clinical Research

Spire Orthopedic Partners•Wakefield, RI

1d•Onsite

About The Position

The Vision of the Clinical Researcher is the essential link in providing a team-based approach to patient care and an exceptional patient experience. The Clinical Researcher will emphasize highly personalized care and help patients surpass barriers to healthcare by improving the patient/provider relationship. The Clinical Researcher is responsible for the coordination and administration of clinical trials under the direction of the Principal Investigator. The Clinical Researcher will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials. The Clinical Researcher will perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study specific protocols.

Requirements

Bachelor's degree in Human Health Care or related field required.
Any combination of education, training, and experience that demonstrates the ability to perform the duties of the position.
Experience with Electronic Medical Records
Excellent computer skills
EMR Systems
Practice Management System
Microsoft Suite (including: Outlook, Word, Excel, Calendar)
Phone software
Navigating Insurance Authorization websites
Knowledge of estimated co-payment and co-insurance
General understanding of processing legal forms
Ability to collaborate with supervisory teams and administrators on projects or assigned tasks

Nice To Haves

Spine, Joints/Trauma, Sports Medicine, Foot/Ankle, and Hand/Microsurgery

Responsibilities

Collect and organize data and compile for progress reports
Coordinate with research assistants/ student employees, provide guidance and assistance as needed
Assist and coordinate with Research Manager to ensure clinical research and activities are performed in accordance with approved IRB
Discuss study protocols with patients and verify the informed consent documentation
Provide patient with written communication of their participation (i.e. copy of the signed informed consent)
Adhere to Good Clinical Practices and the study protocols
Ensure scientific integrity and accuracy of data and protect the rights, safety, and well-being of patients enrolled in clinical trials
Prepare findings for publication and assist in laboratory analysis, quality control, or data management
Write and contribute to publications
Ensure that non-serious and serious adverse events are properly documented and reported
Liaison to partnering hospitals other research sites for new and existing patients
Prepare and submit initial review of new studies to IRB
Assist with overflow Medical Assistant duties
Compliance with HIPAA and OSHA regulations
Other duties may be assigned as necessary