Oncology Clinical Research Lead (Remote)

Sumitomo Pharma; Juneau (AK); À distance; USD 226 000 - 282 000; Plein temps

Résumé du poste

Sumitomo Pharma America is seeking an Associate Medical Director, Clinical Development – Oncology to lead and manage clinical studies, partnering with investigators and KOLs worldwide. The role emphasizes hematologic malignancies and cross-functional collaboration in a fast-paced environment.

Responsibilities include protocol design, data review, safety assessment, and contributions to IND/NDAs, with remote work from the US and periodic on-site meetings. Competitive compensation provided.

Qualifications

• MD/DO or non-US equivalent required.
• Residency completion strongly preferred.
• Subspecialty fellowship desirable.
• Experience in hematological malignancies or solid tumors desirable.
• 0 to 3 years of pharmaceutical drug development experience required.

Responsabilités

• Design and implement clinical protocols aligned with product development plans, focusing on hematologic malignancies.
• Provide clinical input to protocols, regulatory documents, publications, and investigator interactions.
• Lead clinical study teams, monitor study integrity, and review safety/efficacy data.
• Contribute to regulatory filings with clinical sections for INDs/NDAs.
• Collaborate with Drug Safety & Pharmacovigilance to assess safety profiles.

Connaissances

Hematologic malignancies knowledge

Clinical trial methodology

Leadership

Communication

Team collaboration

Formation

MD/DO or non-US equivalent

Residency completed

Subspecialty fellowship desirable

Experience in blood cancers or solid tumors desirable

Pharmaceutical drug development experience 0–3 years

Description du poste

Sumitomo Pharma America is seeking an Associate Medical Director, Clinical Development – Oncology to lead and manage clinical studies, partnering with investigators and KOLs worldwide. The role emphasizes hematologic malignancies and cross-functional collaboration in a fast-paced environment.

Responsibilities include protocol design, data review, safety assessment, and contributions to IND/NDAs, with remote work from the US and periodic on-site meetings. Competitive compensation provided.