Provide medical monitoring for assigned projects
Function as medical representative on the project team
Provide medical consultation as required or requested to client/sponsor or to other Parexel service groups
Assume the role of Senior Technical Lead in selected circumstances
Review all individual adverse experience reports for accuracy and clinical importance
Characterize relationship to the study drug, severity, and seriousness
Provide reports to FDA or other regulatory agencies and the sponsor summarizing adverse experiences as required
Review data listings of safety data, including adverse experiences, laboratory data, and vital signs data
Review documents for safety issues written by various Parexel divisions
Provide support for preparation of clinical protocols, integrated clinical and statistical summary reports, journal articles, and other documents

Medical Degree from an accredited institution
Board Certification / Fellowship in Hematology / Oncology
2+ years of experience in adult Hematology required
Experience in CAR-T, Myeloma or Lymphoma highly preferred
Prior experience as a Medical Monitor, Industry Physician, Primary Investigator, or Sub-Investigator highly preferred
Strong interpersonal skills and the ability to collaborate effectively with sponsor and client partners
Excellent time‑management capabilities
Clear, professional verbal and written medical communication skills
A high standard of written and spoken English
Comfort working in a matrixed, team‑oriented environment
Willingness to travel up to 15% domestically and/or internationally as needed

Medical Director, Hematology/Oncology

Key skills