About the Opportunity
We are partnered with a rapidly growing organization with a focus in Oncology / Hematology that is looking to bring on a Senior Medical Director, Clinical Development (Medical Monitoring). This is a full-time, remote position that can be located anywhere in the United States. This individual will provide hands-on medical monitoring and clinical expertise to support the design, conduct, and interpretation of clinical trials. Acting as the primary Medical Monitor for assigned studies, the Medical Director serves as a key medical point of contact for investigative sites and sponsors, providing real-time medical guidance, reviewing safety data, and contributing to clinical and scientific discussions to support high-quality study execution.
The annual base salary range is $280,000 to $320,000. Actual compensation offered to the successful candidate may vary from posted hiring range based upon geographic location, work experience, education, and/or skill level, among other things. Details about eligibility for bonus compensation (if applicable) will be finalized at the time of offer.
Job Responsibilities
- Serve as the primary Medical Monitor for assigned clinical trials
- Act as the first point of contact for investigative sites for medical questions related to eligibility, enrollment, and patient management
- Review and interpret safety data including serious adverse events (SAEs), adverse events (AEs), laboratory data, medical history, and concomitant medications
- Provide medical input into protocol development, protocol amendments, and study-related documents
- Contribute to development of Medical Monitoring Plans and Safety Management Plans
Job Requirements
- Doctor of Medicine (MD) from an accredited institution. A strong foundation in clinical medicine, combined with practical experience in medical research or clinical development, is essential. Additional certifications or training in specific therapeutic areas (e.g., hematology, oncology) may be an advantage, but the primary qualification must be an MD or equivalent medical degree
- Minimum of 10–15 years of experience in clinical development, including significant experience in medical monitoring and clinical trial oversight
- Prior experience serving as a Medical Monitor on Phase I–IV clinical trials in a pharmaceutical, biotechnology, or CRO setting
- Strong knowledge of clinical trial methodology, safety assessment, and medical data review
- Therapeutic area expertise in oncology, hematology, or related fields preferred
