Senior Medical Director, Medical Affairs (Oncologist) - U.S. Remote

Worldwide Clinical Trials - USA; North Carolina; Remote; USD 150,000 - 210,000; Full time

Job summary

An innovative organization is seeking a Senior Medical Director with oncology expertise to lead medical oversight in clinical trials. This pivotal role offers the chance to engage in the entire lifecycle of clinical investigations, from protocol preparation to regulatory submissions. The ideal candidate will ensure data integrity and contribute to clinical development programs while mentoring junior staff. Join a forward-thinking team dedicated to improving lives through groundbreaking research and collaboration. If you're passionate about making a difference in healthcare, this opportunity is perfect for you.

Qualifications

• 3-6 years of medical monitoring experience in a CRO or pharmaceutical setting.
• Strong expertise in medical data review and ensuring data quality.

Responsibilities

• Provide medical oversight for oncology clinical trials and serve as Medical Monitor.
• Conduct medical data reviews and support business development activities.

Skills

Medical Oversight

Medical Data Review

Organizational Skills

Communication Skills

Presentation Skills

Education

Medical Degree with board certification in oncology

Fellowship training in medical oncology

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

Senior Medical Director, Medical Affairs (Oncologist) - U.S. Remote

Employer: Worldwide Clinical Trials - USA

Location: Virtual United States

Salary: Competitive

Start date: 5 Mar 2025

Closing date: 15 Apr 2025

Who we are
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 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.

What Medical Affairs 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
At Worldwide Clinical Trials, we push boundaries and innovate to find cures for the world’s most persistent diseases. We are seeking a Senior Medical Director with expertise in oncology to join our Medical Affairs team. This role provides medical oversight, contributes to clinical development programs, and supports business development activities.

• Provide medical oversight for oncology clinical trials, serving as Medical Monitor and, when applicable, Global Lead Medical Monitor.
• Conduct medical data review to ensure the integrity, accuracy, and quality of clinical trial data.
• Work closely with pharmacovigilance teams on selected Serious Adverse Events (SAEs) and Suspected Unexpected Serious Adverse Reactions (SUSARs).
• Contribute to the design and execution of clinical development programs, study protocols, and research materials.
• Provide protocol-specific and therapeutic training to project teams.
• Support business development through feasibility assessments, proposal generation, budget development, and sponsor engagement.
• Mentor and guide junior medical staff, exemplifying work ethics, compassion, and integrity.
• Stay abreast of therapeutic and regulatory advancements by attending conferences, reviewing literature, and participating in internal meetings.

What you will bring to the role

• Excellent spoken and written English skills.
• Excellent organizational and time management skills.
• Excellent presentation skills.

Your experience

• Medical Degree with board certification in oncology.
• Fellowship training in medical oncology, including malignant hematology, is required.
• 3-6 years of medical monitoring experience, preferably within a CRO, pharmaceutical, or biotech setting.
• Strong expertise in medical data review and a commitment to ensuring data quality and consistency.
• Strong organizational, communication, and presentation skills, with proficiency in Word, Excel, and PowerPoint.
• Demonstrated ability to manage multiple priorities and collaborate within matrixed study teams.
• Availability to travel domestically up to 20% and flexibility to provide after-hours medical support.

We love knowing that someone is going to have a better life because of the work we do.

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.