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

Fortrea•Madison, WI

13d•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. If you're ready to lead with purpose, grow your expertise, and collaborate with a dynamic team, this role could be your next big move. Role Highlights: Support healthy volunteers by providing onsite medical coverage and oversight Excellent work/life balance M-F schedule 7:30am – 3:30pm schedule variable based on enrollment periods Call Rotation 1:4 (every fourth weekend – from home / come in as needed) Communicate across clinical teams, regulatory bodies & 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

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.
Open to candidates interested in moving to area and obtaining state licensure.
English proficient in speaking, writing, and reading.

Nice To Haves

Clinical trials experience is a plus
Passion for research, safety, and patient-centered care

Responsibilities

Utilizes various technology platforms, databases, and electronic systems to support medical monitoring, data review, clinical trial execution, and communication with internal and external stakeholders.
Conducts final review and approval of Case Report Forms (CRFs) to ensure data accuracy, protocol adherence, and regulatory compliance at study closeout.
Approximately 10–20% of the role may involve administrative and operational activities.
Provides medical training and guidance to cross-functional teams to ensure high standards of clinical practice.
Undertake any other duties as required