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Job type: Permanent

Discipline: VP/Head of Clinical Operations

Location: United States

Vice President Clinical Development, Immuno-Oncology - Permanent - Remote within US

Are you ready to lead cutting-edge clinical development that accelerates clinical breakthroughs in biotech?

̽��ϼ� is seeking a Vice President of Clinical Development to lead the clinical development strategy and execution for a portfolio of innovative immuno-oncology therapeutics.

Primary Responsibilities:

In this role, you will oversee clinical programs, ensuring scientific rigor, regulatory compliance, and operational excellence. This position requires a strong background in regulatory strategies, biometrics, and medical writing, as well as expertise in safety monitoring and pharmacovigilance.

Skills & Requirements:

Medical degree (MD or equivalent).
Extensive experience in clinical development within the biotechnology or pharmaceutical industry, including leadership roles.
Proven ability to manage multiple complex programs or studies.
Comprehensive understanding of clinical trial operations, drug development processes, and global regulatory requirements.
Strong business acumen with the ability to lead and align cross-functional teams.
Exceptional written and verbal communication skills, with the ability to convey complex ideas clearly.
Strategic thinker with strong analytical and problem-solving abilities.
Ability to thrive in a fast-paced, detail-oriented, and entrepreneurial environment.
Proven ability to build and maintain collaborative relationships with internal and external stakeholders.

The Vice President Clinical Developments' responsibilities will be:

Develop and oversee clinical development programs, including strategic planning and execution of clinical trials.
Evaluate and refine development strategies to mitigate risks and accelerate asset advancement.
Lead the planning, delivery, and management of clinical trials across early to late phases.
Design and refine clinical trial protocols, ensuring compliance with scientific, ethical, and regulatory standards.
Provide medical oversight throughout the clinical trial lifecycle, including safety monitoring, data interpretation, and risk management.
Supervise biometrics and medical writing to ensure high-quality study design, analysis, and reporting.
Collaborate with regulatory teams to develop and execute strategies for successful trial approvals and submissions.

Compensation:

$300,000 to $350,000 per annum.

If you are having difficulty in applying or if you have any questions, please contact Tom Pinnock at t.pinnock@proclinical.com

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

̽��ϼ� is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. ̽��ϼ� is acting as an Employment Agency in relation to this vacancy.

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