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Clinical Research Physician

Madison, WI
Closing date
Nov 26, 2022

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Doctors, Pharmaceutical, Physicians/Nurses
Organization Type
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Job Description
Job Summary:

Contributes to the development of Company policies involving medical, safety and therapeutics. Also participates in process improvement activities across Company

Client Relationship & Business Development Activities

• Partnering with GCO to develop new and enhance existing client relationships where possible

• Presents medical/scientific capabilities to clients as a participant of a proposal team

• Performs site/investigator feasibility, builds relationships with investigators to support optimal recruiting and conduct of trials


• Supports and participates in the recruitment process for department positions


• Provides leadership to junior staff within the therapeutic area

• Participates and leads initiatives that serves the physicians within the TA

Therapeutic and Scientific Expertise

• Develops training modules and materials, and provides training in disease states and

protocol specific requirements across the Company

• Participates in training opportunities to advance knowledge of drug development and good

clinical practice guidelines

• Serves as global lead project physician

• Performs medical data review- Reviews laboratory values, adverse events, coding

dictionaries and data tables, listings and figures as needed

• Develops, reviews and revises protocols, case report forms, training materials, project

specific tools, analysis plans design, clinical trial reports and new drug applications

• Prepares materials for investigator meetings

• Actively participates in investigator meetings

• Provides medical/scientific expertise to project teams

• Responsible for medical and safety monitoring on assigned projects

• Interacts with inter-departmental and external consultants as appropriate

• Participates in feasibility discussions relating to specific project proposals

• Participates in project risk assessment activities

• Assists when needed with data safety monitoring board activities

• Provides clinical and medical expertise to other Covance departments

Travel requirements of the position on an annual basis

% of time: 30%

Travel is primarily to where: Global


• 3-5 years of experience with substantial knowledge of drug development and extensive

clinical research experience within the pharmaceutical/CRO industry in a specific

therapeutic area

• Equivalent academic experience can be substituted

Education/Qualifications/Certifications and Licenses:

Minimum Required

• MD Degree


• Relevant sub specialty fellowship training and history of board certification


• Covance Leadership Competencies

• Ability to drive projects outside of medical perspective

• Problem solving ability

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

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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