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

Fortrea Inc

  • Madison, WI
  • 4 days ago
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    Skills

    • Case Report Form (CRF)unmatched
    • Clinical Dataunmatched
    • Clinical Information Systemsunmatched
    • Clinical Laboratoryunmatched
    • Clinical Practices/Protocolsunmatched
    • Clinical Researchunmatched
    • Clinical Trialunmatched
    • Communication Skillsunmatched
    • Computer Skillsunmatched
    • Computer Softwareunmatched
    • Cross-Functionalunmatched
    • Data Qualityunmatched
    • Database Report Toolsunmatched
    • Document Managementunmatched
    • Electrical Componentsunmatched
    • Emerging Technologyunmatched
    • English Languageunmatched
    • Hardware Virtualizationunmatched
    • Health Planunmatched
    • IRB/IEC (Institutional Review Board/Independent Ethics Committee)unmatched
    • Laboratory Equipmentunmatched
    • Laptop PCunmatched
    • Lift/Move 20 Poundsunmatched
    • Medical Office Administrationunmatched
    • Microsoft Excelunmatched
    • Microsoft Officeunmatched
    • Microsoft Outlookunmatched
    • Microsoft Wordunmatched
    • Office Equipmentunmatched
    • Patient Safetyunmatched
    • Quality of Careunmatched
    • Regulatory Complianceunmatched
    • Reporting Skillsunmatched
    • Research Protocolsunmatched
    • Software Developmentunmatched
    • Training/Teachingunmatched
    • United States Drug Enforcement Agency (DEA)unmatched

    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.

    Numbers & Facts

    LocationMadison, WI

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