Clinical Research Coordinator Jobs

- Study Coordinator

A hospital system we are working with is seeking a research Coordinator who can oversee and support the conduct of a pilot program that will last 3-5 months. The candidate will be primarily responsible for launching a groundbreaking remote patient monitoring pilot program. The job is initially short-term but has the opportunity to turn into a long-term role with the hospital.

This Research Coordinator will be responsible for ensuring the successful launch and execution of the remote patient monitoring pilot program. The Research Coordinator will be responsible for working independently and maintaining professional and effective communication with physicians, patients, peers, and other hospital personnel. They must also adhere to the policies and procedures of the hospital they are supporting. The Coordinator's key responsibilities will include:

Platform Integration Management:

●Lead the effort for building out a “Smart Healthcare Platform” that will host the current iTempShield’s program on a secure network

●Ensure remote patient monitoring platforms are integrated between the hospital system and Idion

●Support marketing and promotional efforts for the program

Study Site Management:

●Screen for potential protocol patients and determine patient eligibility for the program

●Oversee subject enrollment to ensure that informed consent is properly obtained and documented.

●Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.

●Clinical study product and device accountability from the administration to completion of the study

●Educates and answers patients questions regarding study device

●Ensures that study is conducted as written so that scientific questions are answered

●Protocol Administration

●Prepare study-related documentation, such as study binders, procedural manuals, visit documentation and training materials

●Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts, such as protocol revisions.

●Ensures study is on track, and builds and follows milestone tracking for study success

●Maintain completeness of site documents and manage patient and study data

●Able to create and edit a study report as needed

●Will primarily be responsible for non-regulated clinical studies, but may be introduced to regulated study activities as appropriate

●Assist other team member participating in the cross-training opportunities with study-related activities

●Support the start-up, monitoring and maintenance of Idion’s other clinical study projects as requested

●Close out clinical study sites on completion of the study

Expected Areas of Competence

●Project management experience- competent in tracking project milestones, owning a project and proactively moving the needle for project success and completion

●Previous clinical trial experience

●Medical device experience

●Ability to present to stakeholders

●Ability to prioritize assignments, manage time efficiently and assist in project oversight to meet established deadlines

●Attention to detail with outstanding organizational skills

●Ability to multi-task in fast paced environment is essential.

●Assists in the efficient use of available resources to accomplish project goals

●Able to adapt behaviors and attitude to improve performance of the team and to have a positive effect on the outcome of the project

●Initiates and exchanges best practices with other team members and business partners

●Possesses positive attitude and self-awareness of impact of actions on others

●Significant understanding and willingness to comply with Regional and Global guidelines (ICH/FDA/MDR) and government related regulations

●Understanding of medical terminology

●Proficient in Microsoft Office including Word, Excel, Project and PowerPoint, Data management platforms, EMR systems

●Willingness to learn and progress

●Above average reading comprehension

●Understanding and willingness to follow Idion’s policies, procedures, standard operating procedures, and work instructions

Education/Experience Requirements

Minimum Education: Bachelor's degree in life or medical sciences, public health, health policy or hospital administration

Minimum Experience: 2-year Minimum Field of Expertise: Project management experience, Hospital Administrative or research experience, Experience navigating healthcare systems, Patient facing experience is a plus

A combination of education and experience may be considered

Location Requirement

Albany/Schenectady Capital District Region

About Us

The IDION Shield is an innovative remote patient monitoring device that empowers healthcare providers to improve patient outcomes for all. IDION is an innovative new technology that acts as a catalyst for the emerging telehealth sector in healthcare. IDION’s mission is to provide a lower-cost, easy to use device that will make remote monitoring widely accessible for patients at little or no-cost to the healthcare provider.

https://www.idion.us/

IDION® is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state or local law.