Senior Medical Director– Oncology - Mid-sized CRO – Homebased USA

i-Pharm Consulting; United States; Remote; USD 330,000 - 387,000; Full time

Job summary

A leading consulting company is seeking a Senior Medical Director specializing in Oncology. This home-based role offers the chance to lead clinical trial strategies while advising on medical matters. Ideal candidates will have extensive experience in Oncology, with board certification preferred. The role is full-time and offers a competitive salary.

Benefits

Medical insurance

401(k)

Vision insurance

Paid maternity leave

Qualifications

• Qualified physician with a board certification or fellowship in Oncology.
• Experience in solid or hematological tumors.
• Experience with CAR-T and cell therapies is a plus.

Responsibilities

• Responsible for scientific and clinical strategy of clinical trials.
• Advise clients, monitoring boards, and regulatory agencies.
• Collaborate with clinical teams for protocol and development plans.

Skills

Expertise in Oncology

Client-facing experience

Education

Board certified in Oncology

Fellowship in Oncology

Job description

Senior Medical Director– Oncology - Mid-sized CRO – Homebased USA

Senior Medical Director– Oncology - Mid-sized CRO – Homebased USA

Senior Medical Director– Mid-sized CRO – Homebased USA

Summary

i-Pharm Consulting are seeking a qualified physician with a strong background in Oncology (ideally board-certified or with a fellowship in Oncology).

This position is a full-time role as a Senior Medical Director with a global mid-sized CRO Client. This position can be homebased anywhere in the US.

As the Senior Medical Director, you will be responsible for the scientific and clinical strategy of assigned clinical trials, scientific monitoring, and reporting of quality data.

Responsibilities:

• Provide expertise as the medical monitor to our client’s clinical project teams and sites that are involved in the trials
• Advise the CRO’s clients, data safety monitoring boards, regulatory agencies and third-party vendors on medical matters as the expert in these area
• In preparation for protocol and clinical development plans, you will collaborate with various teams including the Clinical Operations team and Clinical Project Management team
• Be responsible to review and sign off clinical documents with respect to medical relevance
• Participate in such activities as BID defense meetings and Kick-off meetings with the client

Qualifications

• Board certified in Oncology or a Fellowship in Oncology
• Experience working in solid or haematological tumours, experience in both is an advantage
• Experience with CAR-T and cell therapies is a plus
• Experience in medical practice/patient care
• Experience being client facing in a CRO environment or have previously worked in a Pharmaceutical / Biotechnology company

If you are interested in this role, please contact Aoife Cronin on acronin-pharmconsulting.com

Seniority level

• Seniority level

  Director

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research

• Industries

  Staffing and Recruiting

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Inferred from the description for this job

Medical insurance

401(k)

Vision insurance

Paid maternity leave

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