Senior Medical Director

Celcuity

Remote
Base: $260,000-$350,000 doe; bonus/equity: annual ...
Remote
Medical oversight of service suppliers
Clinical study design and protocol development
Medical monitoring for assigned study
Celcuity is seeking a Senior Medical Director to oversee clinical studies in oncology, focusing on Phase I-III trials. The role involves medical oversight, protocol development, and regulatory compliance, requiring an MD with significant clinical development experience

Job Summary

  • Responsible for providing medical oversight of service suppliers driving ongoing clinical studies and plans and executes the study design protocol development, implementation and monitoring of the company’s new Phase I-III Oncology clinical trials.
  • The position will provide key overall clinical, scientific and/or logistical support to clinical development programs and is responsible for the compliance of the department and the company to regulatory standards and procedures.
  • The successful candidate will be eligible for an annual performance incentive bonus and a new hire equity package, along with various benefits offerings including medical, dental, vision insurance, 401k match, PTO, and several paid holidays.

Matching Summary

Match Score: 85

Celcuity is seeking a Senior Medical Director to oversee clinical studies in oncology, focusing on Phase I-III trials. The role involves medical oversight, protocol development, and regulatory compliance, requiring an MD with significant clinical development experience.

Salary

Base: $260,000-$350,000 DOE; Bonus/Equity: Annual performance incentive bonus and new hire equity package; Benefits: Medical, dental, vision insurance, 401k match, PTO, and several paid holidays

Skills & Requirements

Must-have

  • Medical oversight of service suppliers
  • Clinical study design and protocol development
  • Medical monitoring for assigned study
  • Track drug efficacy and safety profiles
  • Prepare clinical sections of regulatory documents
  • Develop publications and presentations

Nice-to-have

  • Collaborative and team-oriented approach
  • Build strong relationships with co-workers
  • Function at a high level in a team setting
  • Values-based leadership

Key Requirements

  • MD with solid tumor clinical trials experience
  • 8-10 years clinical development experience
  • Phase I-III clinical trial experience
  • Working knowledge of IND/NDA process
  • In depth knowledge of GCP/ICH guidelines

Work Rights

Not specified

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