Senior Medical Director, Clinical Development – Oncology

Syndax Pharmaceuticals

New York (NY)

On-site

USD 375,000 - 398,000

Full time

32 hours ago
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Benefits offered by this job

Equity offering
Annual bonus
Competitive benefits

Job summary

Syndax Pharmaceuticals in New York seeks a Senior Medical Director, Clinical Development to lead clinical development plans, oversee multiple assets, and contribute to regulatory strategy. You will collaborate with cross-functional teams, provide medical monitoring oversight, and drive scientific writing for regulatory submissions.

The role reports to the Executive Medical Director and requires MD or MD/PhD with extensive experience in clinical research, ideally in hematology/oncology.

Qualifications

  • MD or MD/PhD with 5-10 years’ experience in clinical research.
  • Sub-specialty training or board certification in hematology, oncology, or related field preferred.
  • Strong ability to integrate biological knowledge into clinical development strategy.

Responsibilities

  • Develops and implements clinical development plans and study protocols with a multidisciplinary team.
  • Represent clinical development with senior internal and external stakeholders.
  • Provide input for business development opportunities and regulatory strategy development.
  • Oversee clinical trial programs and provide medical monitoring oversight with CROs.
  • Lead scientific writing and review of clinical study reports and regulatory documents.
  • Collaborate with translational medicine for biomarker strategy development and IST strategy.

Skills

Clinical development leadership
Regulatory strategy input
Medical monitor liaison
Hematology/Oncology expertise

Education

MD or MD/PhD

Job description

Syndax Pharmaceuticals in New York seeks a Senior Medical Director, Clinical Development to lead clinical development plans, oversee multiple assets, and contribute to regulatory strategy. You will collaborate with cross-functional teams, provide medical monitoring oversight, and drive scientific writing for regulatory submissions.

The role reports to the Executive Medical Director and requires MD or MD/PhD with extensive experience in clinical research, ideally in hematology/oncology.

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