Sr. Medical Director

Are you a passionate leader with a strong background in clinical development, seeking to make a significant impact in the evolving field of life sciences? This is a fantastic opportunity to join a dynamic organization at the forefront of innovative therapies, where your expertise will help shape the future of healthcare. You will have the chance to lead cross-functional teams, influence key clinical strategies, and work in a fast-paced environment that values your scientific insight and leadership.

Our client is a growing organization specializing in developing groundbreaking medical solutions. They are looking for a senior medical leader to drive their clinical development programs, ensuring the highest standards of safety, scientific integrity, and regulatory compliance. This role offers the unique opportunity to operate at the intersection of science, medicine, and strategic leadership, directly impacting clinical decision-making and regulatory success.

Role Summary:
You will serve as a critical member of the clinical development team, providing strategic medical oversight across multiple therapeutic programs, with a focus on advancing innovative treatments. The role involves collaborating closely with internal teams, external investigators, regulatory agencies, and CROs to ensure clinical trials meet their objectives. This position is onsite, with an emphasis on strong leadership and cross-functional influence to support the organization’s growth and success in bringing novel therapies to market.

Key Responsibilities:

• Lead the development and execution of Clinical Development Plans (CDP).
• Manage the clinical protocol development process, ensuring alignment with CDP objectives.
• Provide medical training and ongoing scientific guidance to the clinical team.
• Oversee clinical operations at trial sites, CROs, and internal staff to maintain high standards of safety and compliance.
• Support data management by reviewing case report forms and providing medical insight.
• Contribute to pharmacovigilance activities, including safety reports and safety monitoring committees.
• Engage with investigators and key opinion leaders to facilitate clinical research and trial recruitment.
• Develop scientific methods for clinical trial design, data collection, and analysis.
• Support regulatory interactions, including INDs and NDA/MAA submissions.
• Review and interpret clinical data continuously and contribute to report writing for global regulatory submissions.

Experience & Requirements:

• MD degree, with board certification in oncology preferred.
• Minimum of 5 years’ experience in clinical trials within the pharmaceutical industry or relevant academic research.
• Proven leadership skills and experience managing cross-functional teams.
• Strong communication skills with the ability to collaborate effectively across departments.
• Experience designing and executing clinical trial strategies in a fast-paced, dynamic environment.

Salary:
This role offers a base salary between $350,000 and $380,000, depending on experience.

Apply now to be part of a growing team shaping the future of innovative healthcare solutions.