Senior Medical Director, Medical Affairs (Oncologist) - U.S. Remote - Raleigh
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.
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 Clinical Trials
Medical Affa irs 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 Affa irs 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 Affa irs , 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 Affa irs , 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 y ou to excel and contribute your unique talents to our mission to impact milli ons 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. As a global, midsize CRO with over 3,500 team members, we are dedicated to improving lives through pioneering approaches implemented with excellence.Join a diverse, inclusive environment where you can thrive while making a meaningful impact.
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
- Excellent computer skills (Word, Excel, Access)
- Excellent spoken and written English skills
- Excellent organizational and time management skills
- Excellent presentation skills
- 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 collaboration 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.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide !For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn .
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’reon a mission to hire thevery bestand 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.