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- Tasks: Lead oncology trials, ensuring high-quality protocols and medical oversight.
- Company: Join Parexel, a leader in clinical research with a collaborative spirit.
- Benefits: Remote work, competitive salary, and opportunities for professional growth.
- Why this job: Make a real difference in patient care through innovative oncology research.
- Qualifications: MD with 4+ years clinical experience; pharma or CRO experience preferred.
- Other info: Dynamic role with potential for significant impact in the medical field.
The predicted salary is between 36000 - 60000 £ per year.
When our values align, there's no limit to what we can achieve. Parexel is currently seeking an experienced Study Physician to join us in either Germany or the UK, you will be assigned to one of our key sponsors in the EMEA region. This is an upcoming role, not an active position.
Working as a Study Physician, you will be medically responsible at the trial level throughout the preparation, conduct and reporting phase of clinical trials. During the clinical trial, you will be responsible for providing medical expertise and medical oversight from the Trial Design Outline to the Clinical Trial Report. This is a core role within the trial team.
Responsibilities:- Dedicated to one client.
- Ensure timely preparation of high medical quality clinical trial protocols, minimising protocol amendments.
- Contribute to trial risk-based quality management, by defining medically relevant data and related risks that are integrated into the quality and risk management plan.
- Co-author Clinical Quality Monitoring plans.
- Perform ongoing reviews of medical data.
- Physician (MD) (ideally with medical thesis), trained in a clinical setting, and minimum of 4 years of active clinical practice experience; specialization in internal medicine or general practice is desirable.
- Experience in pharma industry or CRO in medical or project management or global pharmacovigilance functions/any other relevant medical function ideally in Clinical Development is desirable.
- Understanding of relevant regulations and guidance including ICH-GCP.
- Ideally experienced with data visualization systems and IT systems.
Associate Medical Director / Study Physician - Oncology trials - FSP - Remote in London employer: Parexel
Contact Detail:
Parexel Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Medical Director / Study Physician - Oncology trials - FSP - Remote in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the oncology field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream role.
✨Tip Number 2
Prepare for interviews by brushing up on your medical knowledge and trial processes. We recommend practising common interview questions with a friend or mentor to boost your confidence and ensure you shine during the real deal.
✨Tip Number 3
Showcase your passion for clinical trials! When you get the chance, share your insights on recent developments in oncology or discuss your previous experiences. This will help you stand out as someone who’s genuinely invested in the field.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to connect directly with us.
We think you need these skills to ace Associate Medical Director / Study Physician - Oncology trials - FSP - Remote in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the role of Study Physician. Highlight your relevant experience in clinical trials and any specific oncology expertise you have. We want to see how your background aligns with what we’re looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about this role and how your skills can contribute to our team. Keep it concise but impactful – we love a good story!
Showcase Your Medical Expertise: Since this role requires medical oversight, be sure to emphasise your medical qualifications and any relevant experience in clinical development. We’re looking for someone who can bring their A-game to the trial level!
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just a few clicks and you’re done!
How to prepare for a job interview at Parexel
✨Know Your Stuff
Make sure you brush up on your oncology knowledge and clinical trial processes. Familiarise yourself with the latest trends in oncology trials and be ready to discuss how your experience aligns with the responsibilities outlined in the job description.
✨Showcase Your Experience
Prepare specific examples from your past roles that demonstrate your medical expertise and oversight capabilities. Highlight any relevant projects you've worked on, especially those involving protocol preparation and risk management.
✨Understand the Company
Research Parexel and their values. Be ready to explain why you want to work with them specifically and how your values align with theirs. This shows genuine interest and can set you apart from other candidates.
✨Ask Insightful Questions
Prepare thoughtful questions about the role and the company. Inquire about their approach to trial quality management or how they integrate medical data into their processes. This not only shows your interest but also your understanding of the role's complexities.
