Sr. Medical Director

Join a dynamic organization leading innovation in the life sciences sector, where your expertise can make a significant impact on advancing new therapies and treatments. This is a fantastic opportunity for a senior medical professional to contribute to cutting-edge clinical development efforts within a collaborative environment. If you are passionate about driving scientific progress and shaping the future of healthcare, this role offers an exciting platform to do so.

Our client is a prominent player in the biotechnology and pharmaceutical landscape, supporting the development of novel therapies for a range of indications. They are seeking a highly experienced Senior Medical Director to provide leadership across their clinical development programs. This role is vital in guiding strategic planning, clinical trial execution, and advancing their pipeline of innovative products.

Role Summary:
As a Senior Medical Director, you will be a key member of the clinical development team, interacting with cross-functional departments and external partners. Your leadership will influence the design, implementation, and interpretation of clinical trials, all while ensuring regulatory compliance and scientific excellence. This on-site role offers an opportunity to work closely with global investigators, Key Opinion Leaders, and internal teams, driving forward the organization’s ambitious development goals.

Key Responsibilities:

• Lead the development of strategic plans for clinical indications and product development.
• Manage the creation and review of clinical trial outlines, protocols, and regulatory submission documents.
• Support ongoing medical monitoring of clinical trials, including safety assessments and eligibility criteria evaluation.
• Collaborate with external investigators and Key Opinion Leaders to explore novel indications and therapeutic approaches.
• Provide scientific and medical expertise to internal teams across clinical operations, safety, regulatory, and commercial functions.
• Contribute to the preparation of scientific publications, abstracts, and presentations for conferences.
• Ensure adherence to industry standards and regulatory requirements governing clinical trials.
• Assist in evaluating potential business development opportunities by providing clinical insights.

Experience & Requirements:

• Medical degree (MD), with clinical experience in hematology preferred.
• Significant biotechnology or pharmaceutical industry experience.
• Strong leadership and strategic thinking skills, with excellent communication abilities.
• Proven ability to work effectively in fast-paced, evolving environments.
• Experience working with regulatory agencies and preparing regulatory documents.
• Ability to travel up to 20% for conferences and external meetings.

Salary:
This role offers a base salary between $320,000 and $350,000, depending on experience.

Apply now to be part of a growing team shaping the future of life sciences and making a difference in patient care.