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

Job description

Clinical Research Physician, Dallas Phase I Onsite 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 Key Responsibilities (Include but not limited to): 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 Required Qualifications: MD or DO with an active WI medical license and DEA CPR/ACLS certified 2+ years clinical experience (Family Medicine or Primary Care preferred) Clinical trials experience is a plus Passion for research, safety, and patient-centered care 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. Language skills: English proficient in speaking, writing, and reading. Work Environment: Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment. Occasional drives to site locations, occasional domestic travel. Exposure to biological fluids. Personal protective equipment required such as protective eyewear, garments and gloves. Physical Requirements: Ability to work in an upright and /or stationary position for 6-8 hours per day. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment. Occasional crouching, stooping, with frequent bending and twisting of upper body and neck. Ability to access and use a variety of computer software developed both in-house and off-the-shelf. Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs. Regular and consistent attendance. Varied hours may be required. Benefits: All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), Paid time off (PTO) or Flexible time off (FTO), Company bonus where applicable. Learn more about our EEO & Accommodations request here .