Senior Clinical Director, Clinical Research, Hematology

Role Responsibilities:

• Plan and direct clinical research activities in Oncology (Hematology), managing studies across the clinical development cycle (design, initiation, execution, monitoring, analysis, regulatory reporting, publication).


• Evaluate pre-clinical/translational work for early clinical development plans and Investigational New Drug (IND) applications.


• Develop clinical development strategies for investigational/marketed Hematology drugs.


• Plan clinical trials based on strategy; provide medical oversight and overall conduct of trials.


• Analyze and summarize clinical findings to support safety/efficacy decisions, regulatory submissions, clinical study reports, and publications.


• Participate in internal and joint internal/external research teams; support business development assessments.

Required Qualifications/Skills:

• M.D. or M.D./Ph.D.


• Industry or senior faculty academia experience.


• Minimum 3 years clinical medicine experience.


• Minimum 3 years industry drug development or biomedical research (academia).


• Demonstrated success overseeing clinical studies/protocols; strong scientific scholarship.


• Proven track record in clinical medicine and biomedical research; strong interpersonal and teamwork skills.


• Outstanding verbal/written communication and presentation.

Preferred Qualifications/Skills:

• Board Certified/Eligible in Oncology, Hematology, or related discipline.


• Prior clinical research experience and prior publication.

Travel/Work:

• Travel ~20% of the time.


• Hybrid.

Benefits (if applicable):

• Annual bonus and long-term incentive (if applicable); comprehensive benefits (medical/dental/vision, retirement/401(k), paid holidays/vacation, compassionate and sick days).