Remote Associate Medical Director, Oncology Clinical Dev

Sumitomo Pharma; Dover (DE); Remote; USD 226,000 - 282,000; Full time

Job summary

Sumitomo Pharma America, Inc. is seeking an Associate Medical Director, Clinical Development – Oncology to lead the design, execution and management of oncology clinical studies. You will build relationships with investigators and key opinion leaders while advancing regulatory filings and scientific communication.

The role emphasizes hematologic malignancies and requires medical leadership, cross-functional collaboration, and rigorous study oversight in a fast-paced, global environment.

Qualifications

• MD/DO or equivalent.
• Residency completion preferred.
• Subspecialty fellowship desirable.
• Experience in hematologic malignancies or solid tumors desirable.
• 0–3 years of pharmaceutical drug development experience.

Responsibilities

• Design and implement clinical protocols supporting the product development plan, focusing on hematologic malignancies.
• Provide medical input to protocols, regulatory documents, publications, and site interactions.
• Lead clinical study teams and monitor overall study integrity, safety and efficacy data.
• Present at global scientific, medical, and regulatory meetings.
• Draft manuscripts and collaborate with cross-functional teams to meet publication plans.
• Partner with safety and pharmacovigilance to assess safety profiles.

Skills

Hematologic malignancies knowledge

Clinical trial design

Regulatory knowledge

Leadership

Communication skills

Education

MD/DO or non-US equivalent

Residency completion

Subspecialty fellowship desirable

Experience in blood cancers or solid tumors desirable

Pharma drug development experience 0-3 years

Job description

Sumitomo Pharma America, Inc. is seeking an Associate Medical Director, Clinical Development – Oncology to lead the design, execution and management of oncology clinical studies. You will build relationships with investigators and key opinion leaders while advancing regulatory filings and scientific communication.

The role emphasizes hematologic malignancies and requires medical leadership, cross-functional collaboration, and rigorous study oversight in a fast-paced, global environment.