Senior Medical Director, Medical Affairs, Neurology - U.S Remote

Position: Senior Medical Director, Medical Affairs, Neurology - U.S. - Remote
Location: LaSalle

Senior Medical Director, Medical Affairs, Neurology – U.S. – Remote
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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, a global team of over 3,500+ experts, bright thinkers, dreamers, and doers, and together we are changing the way the world experiences CROs – in the best possible way.

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 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 a Senior Medical Director, Neurology does at Worldwide Clinical Trials

Medical Affairs plays a pivotal role throughout the entire 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.

Collaboration is a cornerstone of Medical Affairs, as you work closely with other functional groups within the Worldwide organization. As a member of our team, you will have the opportunity to engage in the entire spectrum of clinical investigation activities, from initial database construction to the final delivery of project datasets. Within Medical Affairs, you will discover a diverse range of roles, including direct interactions with pharmaceutical companies, protocol preparation, feasibility assessments, training of site staff, medical monitoring, pharmacovigilance, and medical writing.

These roles present ample opportunities for you to excel and contribute your unique talents to our mission to impact millions of patients' lives around the globe.

What You Will Do

Collaborates with the other members of the Medical & Safety project teams to process Serious Adverse Events (SAEs)

Contributes medical input into the design of clinical development programs, study protocols, research papers, client‑focused white papers, etc.

Supports Business Development through participation in proposal generation, feasibility assessments, review of proposals/contracts for medical services, and attendance at meetings with sponsors as directed by department senior management.

Reviews and/or assists in the preparation of final study reports (CSRs), or other study documentation (Protocols, ISS/ISEs, etc.) as directed by senior management.

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, review of relevant therapeutic/clinical literature, and attendance in conferences and meetings.

Assists in the mentoring of other medical staff as directed by Senior Management and by consistently displaying exemplary work ethics, compassion, and integrity, supporting Senior Management’s leadership of both the department and the company.

What You Will Bring To

The Role

Excellent computer skills (Word, Excel, Access)

Excellent spoken and written English skills

Excellent organizational and time management skills

Excellent presentation skills

Your Experience

Medical Degree from an accredited institution of Medical Education with a Neurology focus

At least 2‑4 years of medical monitoring in a CRO

Valid passport and ability to travel as required

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