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Clinical Research Physician

Lincoln, NY
Closing date
Mar 21, 2023

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Doctors, Pharmaceutical, Physicians/Nurses
Organization Type
As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries. Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services paired with regulatory support for the chemical testing and crop protection industries.

Labcorp Drug Development is a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Our unique perspectives are based on decades of scientific, medical and regulatory expertise.

*** This position is not remote***

Are you ready to redefine what's possible, and discover your extraordinary potential at Labcorp Drug Development ?

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.

Our mission is to help our clients bring the miracles of medicine to market sooner -- join us for your next career move.

Job Summary:

Provides coverage for the Labcorp Clinical Research Unit. As Principal Investigator/Sub-Investigator, responsible for assuring the health and welfare of participants. Responsible for performing medical procedures, responsible for proper conduct of study trial, and responsible for all trial related medical decisions

Key Responsibilities:
  • Provides onsite medical coverage for Clinical Research Unit for our Madison, WI site
  • Responsible for protecting the rights, safety and welfare of participants under their care
  • Responsible for ensuring that the clinical trial is conducted according to the investigational plan and all applicable regulations
  • Provide medical and scientific feasibility of all new sponsor inquiries
  • Direct test article administration or dispensation
  • Administers test article to the subjects, or delegates this to nursing staff where appropriate
  • Review and evaluate protocols and provide clinical and scientific support
  • Liaise with sponsor regarding study design and site capabilities
  • 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 by the Medical Director
  • Weekend and off-hours work as necessary


• Relevant sub specialty fellowship training and history of board certification

Travel Requirements:
  • Potential travel for cross-site support needs or training needs


• Leadership Competencies

• Ability to drive projects outside of medical perspective

• Problem solving ability

• Sees issues outside of own remit and is able to escalate

Required Education/Licensures/Certifications:
  • MD or DO degree
  • Active and unrestricted Wisconsin Medical License and DEA (Wisconsin license must be obtained prior to hire date if selected applicant does not currently have one)
  • ACLS/CPR/AED Certified

  • Minimum of 3-5 years of clinic/patient care experience
  • Specialization in Family Medicine and or Primary Care preferred.
  • Previous Clinical Trials experience is preferred
  • Ability to work in a fast-paced environment
  • Strong interpersonal and communication skills

In July 2022, Labcorp announced its intention to spin off its clinical development business as a separate public company, subject to the satisfaction of certain customary conditions. Fortrea will become the new brand identity for our Clinical Development business in connection with the spin-off, which is expected in mid-2023.

We believe that the exceptional is possible when you have the right partner, so we are looking for the right people to help build a transformative force in Clinical Development. www. fortrea. com

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Labcorp 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.

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