Interventional Study Scientist Medical Director-Vaccines

Interventional Study Scientist Medical Director

The Interventional Study Scientist Medical Director will lead the scientific design of interventional clinical studies, medical governance, and interpretation of results within the Medical Affairs organization for assigned asset(s)/indication(s). This role will partner closely with the GML and GMT and is the single point accountability for translating the evidence strategy set by the GMT into appropriate interventional studies. The study designed is expected to fulfill a strategic objective of the clinical development and integrated evidence plan. This role is pivotal in shaping data generation strategies and ensuring clinical trials are conducted with the highest standards of quality, ethics, and efficiency.

The successful candidate will have deep expertise in industry-sponsored clinical research, global medical affairs, commercial acumen, and cross-functional team leadership. They will oversee multiple projects independently and may be responsible for study development and implementation across an entire therapeutic area. Must possess Vaccines experience.

Key Responsibilities

Strategic Leadership

Scientific Oversight For The Study

Outputs For The Study

Team Leadership

Regulatory And Compliance

Stakeholder Engagement

Innovation And Continuous Improvement

Basic Qualifications

Advanced degree in a relevant scientific discipline (MD, PhD, PharmD, or equivalent)

Vaccines Medicine experience is required

10 + years of experience in clinical research, with 5 + years in a leadership role overseeing interventional studies

Led at least three large-scale interventional clinical trials from design to execution with demonstrated impact

5+ years of experience as a medical monitor, overseeing at least three interventional clinical trials in compliance with ICH-GCP, FDA, EMA, and other global regulatory requirements

Experience analyzing and synthesizing data from multiple sources to drive decision-making

5+ years of experience leading cross-functional line or matrix teams at the study level, including managing direct reports or leading virtual teams

Evidence of strong leadership skills

Leading the resolution of at least two significant trial challenges

Experience managing multiple priorities in a fast-paced environment

Preferred Qualifications

Physicians and specialization in relevant therapeutic area preferred

Experience collaborating with regulatory authorities

Familiarity with innovative approaches in clinical trial execution

Experience in developing scientific content for publications and regulatory submissions

Understanding of digital tools and AI-driven methodologies for evidence generation

Prior experience with cross-functional teams in a pharmaceutical or biotech setting

The annual base salary for new hires in this position ranges from $170,250 to $283,750 taking into account a number of factors including work location within the US.