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JOB REQUIREMENTS: As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe. Are you ready to redefine what\'s possible, and discover your extraordinary potential at Fortrea ? Joining our team as a Clinical Research Physician will offer you a rewarding career, an opportunity to work in a high-energy & collaborative work place, along with access to comprehensive benefits. With the support of exceptional people from across the globe and an energized purpose, you\'ll be empowered to own your career journey with mentoring, training and personalized development planning. Key Responsibilities (include but not limited to): Provides onsite medical coverage for Clinical Research Unit for our Madison, WI site Protect the rights, safety and welfare of participants under their care Ensure that the clinical trial is conducted according to the investigational plan and all applicable regulations Administers test article to the subjects, or delegates this to nursing staff where appropriate Review and evaluate protocols and provide clinical and scientific support Interact with regulatory bodies as is relevant to clinical operations Attend study initiation meetings. Present protocols at IRB/IEC meetings, as required Assist Operations and Client Managers with sponsor visits Perform pre-study physical examinations and review lab data and all inclusion/exclusion criteria to ensure volunteers are medically and mentally fit upon entering the study Perform on-study and post-study physical examinations to ensure that the physical and mental well-being of volunteers is undiminished at the end of the study Inform Principal Investigator, IRB/IEC and Sponsor as appropriate of relevant events Review and sign CRFs at the conclusion of the study Delegate the above as appropriate Act as Principal Investigator/Co-Investigator as assigned... For full info follow application link. As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply. ***** APPLICATION INSTRUCTIONS: Apply Online: ipc.us/t/8DE9EA47BF734E08