Senior Medical Lead

Key Responsibilities

Lead the clinical development strategy and execution of Zenitars US and global hematology/oncology programs.

Serve as the senior medical representative in FDA and other health authority interactions.

Build and maintain relationships with leading investigators and KOLs.

Provide medical and strategic oversight of clinical trials including protocol development benefit-risk assessment safety governance and data interpretation.

Lead and oversee the US clinical team CROs medical monitors and other external partners.

Support regulatory submissions including IND amendments End-of-Phase meetings NDA/BLA preparation and responses to health authority questions.

Provide clinical input to corporate strategy business development board discussions and investor communications.

Establish appropriate clinical governance quality standards and decision-making processes within a fast-paced biotech environment.

Key Qualifications

MD or equivalent medical degree; board certification or advanced training in hematology/oncology is strongly preferred.

12 years of innovative drug clinical development experience including at least 5 years in hematology/oncology.

Demonstrated leadership experience in sponsor-side Phase 2 and/or Phase 3 clinical development.

Prior experience leading a myelofibrosis or broader MPN program ideally involving a JAK inhibitor is highly preferred.

Proven experience leading FDA interactions and cross-functional global development teams.

NDA/BLA or other late-stage regulatory submission experience is strongly preferred.

Established relationships with leading US MF/MPN investigators would be a significant advantage.

Ability to operate both strategically and hands-on in a small growth-stage biotechnology company.