Senior Medical Director, Clinical Development
Confidential · Chicago, IL
FULL-TIME
Posted Jul 1, 2026
Job Description
About the Company
Join a rapidly growing organization that is making significant strides in the oncology and hematology fields. Be part of an innovative team dedicated to advancing healthcare.
About the Role
We are eager to find a Senior Medical Director for Clinical Development with a specialization in medical monitoring. In this role, you will provide essential medical monitoring and clinical expertise to enhance the design, conduct, and interpretation of clinical trials. Responsibilities include:
• Serving as the primary medical monitor for assigned studies.
• Acting as the main medical point of contact for investigative sites and sponsors.
• Providing real-time medical guidance to ensure the highest quality of study execution.
• Reviewing and interpreting safety data while contributing to clinical and scientific discussions.
To be successful in this role, candidates should hold a Doctor of Medicine (MD) from an accredited institution, with a solid grounding in clinical medicine and practical experience in medical research or clinical development. We require a minimum of 10-15 years of experience in clinical development, especially in medical monitoring and trial oversight. Candidates with prior experience in Phase I-IV clinical trials within the pharmaceutical, biotechnology, or CRO settings will be given preference. Familiarity with clinical trial methodology, safety assessments, and medical data review is essential. Expertise in oncology, hematology, or related therapeutic areas is highly preferred, and additional certifications or training in these fields will be advantageous.
Travel Percent
Less than 10%
Functions
• Medical Care/Hospital Administration
Join a rapidly growing organization that is making significant strides in the oncology and hematology fields. Be part of an innovative team dedicated to advancing healthcare.
About the Role
We are eager to find a Senior Medical Director for Clinical Development with a specialization in medical monitoring. In this role, you will provide essential medical monitoring and clinical expertise to enhance the design, conduct, and interpretation of clinical trials. Responsibilities include:
• Serving as the primary medical monitor for assigned studies.
• Acting as the main medical point of contact for investigative sites and sponsors.
• Providing real-time medical guidance to ensure the highest quality of study execution.
• Reviewing and interpreting safety data while contributing to clinical and scientific discussions.
To be successful in this role, candidates should hold a Doctor of Medicine (MD) from an accredited institution, with a solid grounding in clinical medicine and practical experience in medical research or clinical development. We require a minimum of 10-15 years of experience in clinical development, especially in medical monitoring and trial oversight. Candidates with prior experience in Phase I-IV clinical trials within the pharmaceutical, biotechnology, or CRO settings will be given preference. Familiarity with clinical trial methodology, safety assessments, and medical data review is essential. Expertise in oncology, hematology, or related therapeutic areas is highly preferred, and additional certifications or training in these fields will be advantageous.
Travel Percent
Less than 10%
Functions
• Medical Care/Hospital Administration
Additional Details
- City
- Chicago
- State
- Illinois
- Country
- US
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