Clinical Research Physician - MD for Phase I Site, Madison WI

Fortrea•Madison, WI

4d•Onsite

About The Position

Fortrea is hiring a dynamic Clinical Research Physician at our Madison, WI Phase I site — onsite, full-time, and fully immersed in cutting-edge clinical trials. This role offers an excellent work/life balance with a Monday-Friday schedule, though hours can be variable based on enrollment periods. The position involves a 1:4 call rotation (from home, with potential to come in as needed). The physician will communicate across clinical teams, regulatory bodies, and trial participants, support study protocols, IRB/IEC meetings, and client visits, and conduct pre-, on-, and post-study exams. The role may also involve serving as a Sub- or Principal Investigator.

Requirements

MD or DO with an active WI medical license and DEA.
CPR/ACLS certified.
2+ years clinical experience (Family Medicine or Primary Care preferred).
Demonstrated computer proficiency and strong working knowledge of Microsoft Office Suite, including Outlook, Word, Excel, e-signatures and Teams.
Strong technical aptitude and ability to effectively utilize clinical systems, databases, reporting tools, and emerging technologies in a fast-paced environment.
Ability to manage electronic documentation, prepare reports, and communicate effectively through virtual collaboration platforms.
English proficient in speaking, writing, and reading.

Nice To Haves

Clinical trials experience is a plus.
Passion for research, safety, and patient-centered care.
Open to candidates interested in moving to area and obtaining state licensure.

Responsibilities

Provide onsite medical coverage and oversight for healthy volunteers.
Communicate across clinical teams, regulatory bodies, and trial participants.
Support study protocols, IRB/IEC meetings, and client visits.
Conduct pre-, on-, and post-study exams.
May serve as Sub- or Principal Investigator.
Utilize various technology platforms, databases, and electronic systems to support medical monitoring, data review, clinical trial execution, and communication with internal and external stakeholders.
Conduct final review and approval of Case Report Forms (CRFs) to ensure data accuracy, protocol adherence, and regulatory compliance at study closeout.
Provide medical training and guidance to cross-functional teams to ensure high standards of clinical practice.
Undertake any other duties as required.