Senior Medical Director, Medical Affairs, Oncology - Western Europe - Remote

Overview

Senior Medical Director, Medical Affairs, Oncology - Western Europe - Remote

Join to apply for the Senior Medical Director, Medical Affairs, Oncology - Western Europe - Remote role at Worldwide Clinical Trials.

About Worldwide

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers. Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit. We are a diverse and inclusive environment that promotes collaboration and creativity.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!

What Medical Affairs Does At Worldwide

Medical Affairs plays a pivotal role throughout the life cycle of a clinical investigation, exerting its influence from the initial stages of Business Development to the final Regulatory Submissions. Within this multifaceted domain, the dedicated members of the Medical Affairs team provide essential support to the broader project team, contributing to the cultivation of the scientific and medical principles that define Worldwide's philosophy.

What You Will Do

• Serves as Global Lead Medical Monitor (GLMM) for pan-regional and / or global trials, providing therapeutic and protocol-specific training to the project teams.
• Contributes medical input into the design of clinical development programs, study protocols, research papers, client-focused white papers, etc.
• Maintains a high level of competence with assigned projects, including knowledge of project and therapeutic advances as well as marketplace developments by participating in internal meetings, reviewing relevant literature, and attending conferences and meetings.
• Assists in the annual attainment of departmental revenue targets and any other activities as directed by senior management.

Your Experience

Your Skills and Qualifications

Equal Opportunity

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.

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