Medical Director, Oncology & Hematology

Are you passionate about advancing Oncology clinical development?

Would you relish the challenge of working within a leading global organization; one where you will enjoy a high level of responsibility and autonomy, whilst able to focus on further enhancing your therapeutic expertise?

Our client has enjoyed unprecedented growth and success in the delivery of innovative drug development solutions across all phases and therapeutic areas.

They have a presence in 80 countries globally, with over 10,000 highly qualified staff and have contributed to in excess of 3,500 clinical studies and consulting projects since 2010. During this time they have made a significant contribution to the development of over 100 marketed drugs and conducted pivotal trials leading to the regulatory approval of in excess of 50 compounds.

Much of their success has been achieved through being a recognized leader in conducting complex, global Oncology / Hematology trials, in every phase and across all indications. Their commitment to Oncology continues:

  • 60% of Medical Directors have Oncology / Hematology experience
  • 80% of CRAs have Oncology / Hematology experience
  • 85% of Project Directors and Project Managers have Oncology / Hematology experience
  • 90% of Clinical Team Leaders have Oncology / Hematology experience

As Medical Director, Oncology you will join the Europe, Asia Pacific and Africa Medical Affairs Team consisting of 25 Medical Directors, of which approximately a third are dedicated to Oncology / Hematology.

The Medical Director will require outstanding communication skills, leadership and a “hands-on” approach, working closely with the other experts within the Medical Affairs team to provide Oncology and Hematology expertise within:

  • Scientific Affairs
  • Medical Affairs
  • Patient Access and Retention Services
  • Safety and Commercialisation Services, including Safety & Risk Management

The scope of responsibility will be broad, providing medical expertise across many areas, including site identification, study feasibility, study design, conduct, analysis and reporting, IAEs and IASs, dossiers for regulatory submission, submissions for marketing authorizations of new medicinal products and supporting the Business Development group.

Corporate growth and success will be mirrored by your own personal and professional growth within this career shaping role, where there will be significant opportunity to personal development.

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