Medical Director/senior Medical Director

Discover new opportunities to grow your career as a

**What to Expect**:

- Client Relationship & Business Development Activities: _
- Develop new and enhance existing client relationships where possible
- Provides leadership and presents medical/scientific capabilities to clients as a participant of a proposal team
- Leverage known and builds new relationships with investigators/sites to performs site/ investigator feasibility and to support optimal recruiting and conduct of trials
- Able to present or serve on panels to represent the company at conferences and scientific meetings.
- Therapeutic and Scientific Expertise_
- Responsible for medical and safety monitoring on assigned projects
- Develops training modules and materials, and provides training in disease states and protocol specific requirements
- Participates in training opportunities to advance knowledge of drug development and good clinical practice guidelines
- Serve as global lead project physician and provides clinical and medical expertise
- May serve as a program level physician across multiple studies for a given company
- Performs medical data review and/or oversight of central medical data review
- laboratory values, adverse events, coding dictionaries and data tables, listings and figures as needed, holistic and aggregated data review
- Actively participates in investigator meetings
- Provides medical/scientific expertise to project teams and to other Labcorp Drug Development departments
- 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
- Contributes to the scientific strategic leadership for the programs

**Education / Experience**:

- MD degree with fellowship training in Hematology / Oncology
- Board certification preferred.
- Excellent communication and interpersonal skills
- Ability to travel

**Qualifications**:

- 3+ years of clinical research experience with a CRO, pharmaceutical company, research experience in academics preferred - Strong knowledge and experience with clinical trials
- Previous experience in medical practice/patient care
- Prior clinical / laboratory research experience in a fellowship / academic setting also preferred

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.

**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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