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For Companies At a Glance
- Tasks: Lead clinical trials, ensuring high medical quality and oversight throughout the process.
- Company: Join Parexel, a leader in clinical research and drug development.
- Benefits: Enjoy a hybrid work model with flexibility and a focus on work-life balance.
- Why this job: Make a real impact in healthcare while working with top-tier clients in a collaborative environment.
- Qualifications: MD with 4+ years of clinical experience; pharma or CRO experience is a plus.
- Other info: Opportunity to co-author clinical plans and engage in risk management.
The predicted salary is between 43200 - 72000 £ per year.
Parexel is currently seeking an experienced Study Physician to join us in the UK, you be assigned to one of our key sponsors in the EMEA region. The successful applicant is expected to be office based (Bracknell/Reading) for 2 days per week.
Working as a Study Physician you will be medically responsible at the trial level throughout the preparation, conduct and reporting phase of clinical trial. During the clinical trial, you will be responsible to provide medical expertise and medical oversight from the Trial Design Outline to the Clinical Trial Report. This is a core role within the trial team.
Some Specifics About This Advertised Role
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Dedicated to one client.
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Ensure timely preparation of high medical quality clinical trial protocols, minimising protocol amendments.
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Contribute to trial risk based quality management, by defining medically relevant data and related risks are integrated into the quality and risk management plan.
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Co-author Clinical Quality Monitoring plans.
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Performing ongoing reviews of medical data.
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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.
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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.
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Understanding of relevant regulations and guidance including ICH-GCP.
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Ideally previous experience as a medical monitor
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Ideally experienced with data visualization systems and IT systems.
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*Clinical development/trials experience which would be an additional asset
Lifelancer
Study Physician/Medical Monitor - FSP - Hybrid employer: Lifelancer
Contact Detail:
Lifelancer Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Study Physician/Medical Monitor - FSP - Hybrid
✨Tip Number 1
Make sure to familiarize yourself with the specific clinical trial protocols and regulations, especially ICH-GCP. This knowledge will not only help you during the interview but also demonstrate your commitment to the role.
✨Tip Number 2
Network with professionals in the pharma industry or CROs. Attend relevant conferences or webinars where you can meet people who work in clinical development; they might provide insights or even referrals for the position.
✨Tip Number 3
Highlight any experience you have with data visualization systems and IT tools in your discussions. Being able to showcase your technical skills can set you apart from other candidates.
✨Tip Number 4
Prepare to discuss your previous experiences in medical oversight and how you've contributed to trial quality management. Real-life examples will illustrate your expertise and fit for the role.
We think you need these skills to ace Study Physician/Medical Monitor - FSP - Hybrid
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Study Physician position at Parexel. Understand the key responsibilities and required qualifications, such as experience in clinical trials and knowledge of ICH-GCP.
Highlight Relevant Experience: In your CV and cover letter, emphasize your medical background, particularly any experience in clinical development or as a medical monitor. Mention specific projects or trials you have worked on that align with the role.
Tailor Your Application: Customize your application materials to reflect the language and requirements mentioned in the job description. Use keywords related to medical oversight, trial management, and quality assurance to demonstrate your fit for the role.
Proofread Your Documents: Before submitting your application, carefully proofread your CV and cover letter for any errors or inconsistencies. A polished application reflects your attention to detail, which is crucial in the medical field.
How to prepare for a job interview at Lifelancer
✨Show Your Medical Expertise
Be prepared to discuss your medical background in detail. Highlight your experience in clinical practice and any relevant specialization, especially in internal medicine or general practice. This will demonstrate your capability to handle the responsibilities of a Study Physician.
✨Familiarize Yourself with Regulations
Make sure you understand ICH-GCP guidelines and other relevant regulations. Being able to discuss these during the interview will show that you are well-prepared and knowledgeable about the standards expected in clinical trials.
✨Discuss Risk Management Strategies
Prepare to talk about how you would approach trial risk-based quality management. Share examples from your past experiences where you defined medically relevant data and integrated it into quality and risk management plans.
✨Highlight Your Team Collaboration Skills
As a core role within the trial team, emphasize your ability to work collaboratively. Discuss any previous experiences where you co-authored clinical quality monitoring plans or worked closely with other team members to ensure high-quality outcomes.
