Remote Associate Medical Director, Oncology

Sumitomo Pharma; Frankfort (KY); Remote; USD 226.000 - 282.000; Vollzeit

Benefits dieser Stelle

401(k) plan

Medical insurance

Dental insurance

Vision insurance

Life insurance

Disability insurance

Flexible paid time off

11 paid holidays

Paid sick time

Zusammenfassung

Sumitomo Pharma America, Inc. seeks an Associate Medical Director, Clinical Development – Oncology to lead the design, execution, and interpretation of oncology trials from early development to regulatory submissions. You will provide medical input, supervise study teams, and collaborate with investigators, KOLs, and stakeholders.

Remote work with periodic on-site meetings is expected. The role requires an MD/DO and oncology trial experience, with opportunities to influence regulatory filings

Qualifikationen

• MD/DO or non-US equivalent required.
• Residency completed; subspecialty fellowship desirable.
• Experience in hematologic malignancies or solid tumors desirable.
• 0 to 3 years pharmaceutical drug development experience required.

Aufgaben

• Demonstrate ownership of the design and implementation of a clinical protocol supporting the product development plan, with emphasis on hematological malignancies.
• Provide clinical and medical input to protocols, regulatory documents, publications, and site interactions.
• Lead clinical study teams and monitor study integrity, safety and efficacy data.
• Contribute to regulatory filings including INDs, NDAs, and related documents.
• Collaborate with discovery to design translational strategies as needed.
• Present at scientific, medical, and regulatory meetings globally.

Kenntnisse

Clinical trial leadership

Hematologic malignancies knowledge

Regulatory strategy

Cross-functional collaboration

Excellent communication

Ausbildung

MD/DO or foreign equivalent

Residency completion

Subspecialty fellowship desirable

Experience in hematologic malignancies or solid tumors desirable

Jobbeschreibung

Sumitomo Pharma America, Inc. seeks an Associate Medical Director, Clinical Development – Oncology to lead the design, execution, and interpretation of oncology trials from early development to regulatory submissions. You will provide medical input, supervise study teams, and collaborate with investigators, KOLs, and stakeholders.

Remote work with periodic on-site meetings is expected. The role requires an MD/DO and oncology trial experience, with opportunities to influence regulatory filings