Global Oncology Medical Director, Clinical Development (Hybrid)

Millipore Corporation; Billerica (MA); Hybrid; USD 201,000 - 301,000; Full time

Benefits offered by this job

Health insurance

PTO

Retirement contributions

Perquisites

Job summary

EMD Serono in Billerica, MA is seeking a Medical Director for Global Clinical Development Oncology to provide clinical and scientific leadership across oncology programs, including targeted therapies and ADCs. The role involves cross-functional collaboration and oversight from early to late-phase trials, with emphasis on regulatory submissions and Health Authority interactions.

The position is onsite/hybrid in the Boston area, requiring MD with substantial industry experience in clinical R&D.

Qualifications

• MD with expertise in clinical drug development.
• Experience in oncology.
• Industry experience in clinical R&D within pharma/biotech.
• Experience across Phase 1 through Phase III.
• Proficient in regulatory submissions and Health Authority interactions.

Responsibilities

• Lead assigned clinical studies from Phase 1 through Phase III and support registration-enabling activities.
• Integrate clinical, translational, biomarker, and emerging data to influence indication and dose strategy.
• Collaborate with cross-functional teams across Global Project Teams and Program Leadership.
• Support study design, patient selection, and indication prioritization.
• Review safety and efficacy data to inform development decisions; author key clinical/regulatory documents.

Skills

Oncology expertise

Clinical drug development

Regulatory submissions

Cross-functional collaboration

Study design & management

Data integration biomarker

English communication

Education

MD in Medicine

Job description

EMD Serono in Billerica, MA is seeking a Medical Director for Global Clinical Development Oncology to provide clinical and scientific leadership across oncology programs, including targeted therapies and ADCs. The role involves cross-functional collaboration and oversight from early to late-phase trials, with emphasis on regulatory submissions and Health Authority interactions.

The position is onsite/hybrid in the Boston area, requiring MD with substantial industry experience in clinical R&D.