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- Tasks: Lead global medical monitoring for oncology trials and contribute to clinical development.
- Company: Join Worldwide Clinical Trials, a pioneering CRO dedicated to improving lives through innovative research.
- Benefits: Enjoy remote work flexibility, a supportive team culture, and opportunities for professional growth.
- Why this job: Make a real impact in healthcare while working in a diverse and inclusive environment.
- Qualifications: Medical Degree, Oncology/Hematology Board Certification, and 6-8 years in CRO or Pharma.
- Other info: Be part of a mission-driven team that values creativity and collaboration.
The predicted salary is between 43200 - 72000 £ per year.
Senior Medical Director, Medical Affairs, Oncology – Western Europe – RemoteEurope –
Join to apply for the Senior Medical Director, Medical Affairs, Oncology – Western Europe – RemoteEurope – role at Worldwide Clinical Trials
Senior Medical Director, Medical Affairs, Oncology – Western Europe – RemoteEurope –
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Join to apply for the Senior Medical Director, Medical Affairs, Oncology – Western Europe – RemoteEurope – role at Worldwide Clinical Trials
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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.
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
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.
What You Will Do
- Serves as Global Lead Medical Monitor (GLMM) for pan-regional and/ or global trial(s) to which s/he is assigned, 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 (company-wide project tracking, medical management meeting, etc), review of relevant therapeutic/clinical literature, and attendance in conferences and meetings
- Assists in the annual attainment of departmental revenue targets and any other activities as directed by senior management
What You Will Bring To The Role
- Experience reviewing and/or assisting in the preparation of final study reports (CSRs), or other study documentation (Protocols, ISS/ISEs etc,) as directed by senior management.
- Proven track record of independently supporting 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
- Exhibits the necessary skillset to mentor other medical staff as directed by Senior management and by consistently displaying exemplary work ethics, compassion and integrity, support Senior Management’s leadership of both the department and the company
- Robust clinical/therapeutic acumen in medical subspecialty
- Working knowledge of GCPs and regulatory requirements relating to clinical development and safety assure compliance with ethical, legal and regulatory standards.
Your Experience
- Medical Degree from an accredited institution of Medical Education.
- Oncology/Hematology Board Certification
- 6-8 years in the CRO, Pharma or Biotech industry with the medical monitoring or study physician role.
- Valid passport and ability to travel if required.
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 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’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.
Seniority level
-
Seniority level
Not Applicable
Employment type
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Employment type
Full-time
Job function
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Job function
Health Care Provider
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Industries
Research Services
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Senior Medical Director, Medical Affairs, Oncology - Western Europe - Remote employer: Worldwide Clinical Trials
Contact Detail:
Worldwide Clinical Trials Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Medical Director, Medical Affairs, Oncology - Western Europe - Remote
✨Tip Number 1
Network with professionals in the oncology field, especially those who have experience in medical affairs. Attend relevant conferences and seminars to meet potential colleagues and learn about the latest trends in oncology research.
✨Tip Number 2
Familiarise yourself with Worldwide Clinical Trials' mission and values. Tailor your conversations and interactions to reflect how your personal goals align with their commitment to improving lives through innovative clinical trials.
✨Tip Number 3
Stay updated on the latest developments in oncology and medical affairs. Subscribe to industry journals and follow key opinion leaders on social media to ensure you can discuss current topics knowledgeably during interviews.
✨Tip Number 4
Prepare to demonstrate your leadership skills and ability to mentor others. Think of specific examples from your past experiences where you successfully led a team or contributed to a project that required collaboration and guidance.
We think you need these skills to ace Senior Medical Director, Medical Affairs, Oncology - Western Europe - Remote
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in medical affairs, particularly in oncology. Use specific examples of your contributions to clinical trials and any leadership roles you've held.
Craft a Compelling Cover Letter: Your cover letter should reflect your passion for improving patient lives and your alignment with Worldwide Clinical Trials' mission. Mention specific projects or achievements that demonstrate your expertise in the field.
Highlight Relevant Qualifications: Clearly outline your medical degree, board certifications, and years of experience in the CRO, Pharma, or Biotech industry. Emphasise your knowledge of GCPs and regulatory requirements as they relate to clinical development.
Showcase Soft Skills: In addition to technical skills, highlight your ability to mentor others, work collaboratively in teams, and communicate effectively with stakeholders. These qualities are essential for a Senior Medical Director role.
How to prepare for a job interview at Worldwide Clinical Trials
✨Showcase Your Medical Expertise
As a Senior Medical Director, it's crucial to demonstrate your deep understanding of oncology and medical affairs. Be prepared to discuss your previous experiences in clinical development and how they relate to the role. Highlight specific projects where you contributed significantly.
✨Understand the Company's Mission
Worldwide Clinical Trials values innovation and a patient-centric approach. Familiarise yourself with their mission and values, and be ready to explain how your personal values align with theirs. This shows that you're not just looking for a job, but are genuinely interested in contributing to their goals.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills and decision-making abilities in complex situations. Prepare examples from your past experiences where you successfully navigated challenges in clinical trials or medical affairs, showcasing your leadership and strategic thinking.
✨Emphasise Collaboration and Mentorship
The role involves mentoring other medical staff and working closely with diverse teams. Share examples of how you've fostered collaboration in previous roles and how you plan to support and mentor your colleagues at Worldwide Clinical Trials.
