Global Clinical Strategy Director - VP

Proclinical; Delaware; Remote; USD 250,000 - 350,000; Full time

Job summary

Proclinical is seeking a Global Clinical Strategy Development Director - VP Clinical Development to join a dynamic biotechnology team with a global remit in oncology and immuno-oncology. The role is remote and permanent, reporting to the Chief Medical Officer.

You will lead late-stage programs, guide MRCTs, and collaborate with regulatory and cross-functional teams to advance therapies toward registration on a worldwide scale.

Qualifications

• MD degree or equivalent qualification.
• Extensive experience in late-stage development, including Phase III trials.
• Proven track record leading or participating in MRCTs.
• Deep knowledge of global regulatory and clinical development pathways.
• Therapeutic focus on oncology and immuno-oncology.
• Ability to make high-impact decisions in global clinical strategy.

Responsibilities

• Lead late-stage clinical development programs, including Phase III through BLA/NDA submissions.
• Oversee Multi-Regional Clinical Trials (MRCTs), especially in the US and EU.
• Drive global clinical strategy to support product registration.
• Collaborate with cross-functional teams to align regulatory and clinical development pathways.
• Provide strategic input into therapies in oncology, immuno-oncology, autoimmune diseases, and other serious conditions.
• Report directly to the Chief Medical Officer.

Skills

MD degree

Late-stage development

Phase III trials

MRCTs

Regulatory submissions

Oncology & IO focus

Global strategy decisions

Education

MD degree or equivalent

Job description

Global Clinical Strategy Development Director - Permanent - Remote

Are you ready to shape global clinical development strategies and lead late-stage oncology programmes that bring life-changing therapies closer to patients worldwide?

Proclinical is seeking a Global Clinical Strategy Development Director - VP Clinical Development to join a dynamic and innovative team in the biotechnology sector.

Primary Responsibilities:

The successful candidate will focus on advancing clinical strategies for oncology, immuno-oncology, and other severe conditions with unmet medical needs. You will play a pivotal role in late-stage clinical development, contributing to groundbreaking therapies that make a difference in patients' lives.

Skills & Requirements:

• MD degree or equivalent qualification.
• Strong expertise in late-stage clinical development, including hands-on experience with Phase III trials and regulatory submissions.
• Proven track record in leading or participating in MRCTs.
• In-depth knowledge of global regulatory and clinical development pathways.
• Therapeutic focus on oncology and immuno-oncology, with broader interests in autoimmune and severe diseases.
• Demonstrated ability to make impactful decisions in global clinical strategy.

The Global Clinical Strategy Development Director's responsibilities will be:

• Lead late-stage clinical development programs, including Phase III trials through BLA/NDA submissions.
• Oversee and participate in Multi-Regional Clinical Trials (MRCTs), particularly in the US and EU.
• Drive global clinical strategy decision-making to support product registration.
• Collaborate closely with cross-functional teams to ensure alignment with regulatory and clinical development pathways.
• Provide strategic input into the development of therapies in oncology, immuno-oncology, autoimmune diseases, and other serious conditions.
• Report directly to the Chief Medical Officer, contributing to high-level organizational goals.

Compensation:

• $250 000.00 - $350 000.00/Annum