Research – Principal Investigator

at iMETx (view profile)
Location VERONA, WI
Date Posted July 30, 2019
Category Digital Health
Job Type Full-time
Address 8806 ROYAL OAKS DR



Prepares grant proposals and publications.

Assists in the design of and conducts complex research protocols in area of expertise. Oversees and monitors research studies and conducts and/or reviews various phases of research projects and ensures timelines are met. Disseminates research findings to advance the science of the profession. Conducts research experiments and assures the validity and reliability of all collected data.

Collaborates with project teams in developing and implementing routine research plans and protocols, conducting analyses, and preparing reports, abstracts and manuscripts.

In consultation with Senior Research Scientists, monitors the operation of complex technical procedures and equipment.

Designs and/or modifies experimental and routine research and/or patient-related testing procedures.

Participates in the organization and writing of scientific and technical standard operation procedure (SOP) manuals and publications. May co-author and contribute to publications. Disseminates scientific information through publication of manuscripts and presentations.

Performs regular scientific literature searches and maintains current and complete literature referencing.

Participates in the development of Intellectual Property.

Licenses & Certifications

All CiTi bio-medical certificates and HIPPA certificate


Doctorate Degree in Health Science or Medicine or Kinesiology

Outstanding Master’s degree candidates will be considered.

Required Functional Experience

Typically requires 3 years of experience in research, with a minimum of two years post-graduate experience in performing research in a designated field.

Knowledge, Skills & Abilities

Strong critical/analytic thinking and ability to communicate effectively. Understanding of good clinical practices and the laws, regulations, standards and guidance governing the conduct of clinical studies and the preparation of clinical documentation in support of regulatory submissions. Understanding of various computer systems and databases. Experienced in developing and delivering presentations, reports, and business correspondence. Minimum of three peer-reviewed publications. Preferred experience as Principal Investigator, Co-PI or co-investigator. Ability to interact on a scientific level with medical staff and other researchers. Demonstrated effective organizational and time management skills, professional communications, and conflict resolution skills. Knowledge of scientific methodologies, procedures, and basic experimental theories/applications.

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