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- Tasks: Lead safety surveillance and assess safety data in Rare Disease.
- Company: Join a global pharmaceutical company making a difference in rare diseases.
- Benefits: Enjoy a hybrid work model with 3 days on-site each week.
- Why this job: Be at the forefront of safety and risk management in a vital field.
- Qualifications: Medical degree with clinical experience; background in pharmacovigilance preferred.
- Other info: Opportunity to collaborate with cross-functional teams and influence key decisions.
The predicted salary is between 43200 - 72000 £ per year.
BioTalent is collaborating with a global pharmaceutical company to appoint a UK based Global Safety Physician. This is an important position to drive safety and risk management in Rare disease. This is a hybrid role with a typical 3 day per week on site requirement.
Responsibilities:
- Lead safety surveillance and assess integrated safety data in Rare Disease.
- Contribute to benefit-risk assessments and support regulatory submissions.
- Collaborate with cross-functional teams to ensure the highest safety standards.
- Represent safety in internal and external decision-making forums.
Key Requirements:
- Medical degree with proven clinical experience and sound medical judgment.
- Strong background in clinical development or pharmacovigilance, ideally in rare diseases.
- Experience with regulatory submissions (FDA/EMA) or working within regulatory agencies.
If this role is for you reach out to
Global Safety Physician employer: BioTalent
Contact Detail:
BioTalent Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Global Safety Physician
✨Tip Number 1
Make sure to highlight your clinical experience and any specific work you've done in rare diseases during your conversations. This will show that you understand the unique challenges and nuances of this field.
✨Tip Number 2
Familiarize yourself with the latest trends and regulations in pharmacovigilance, especially those related to rare diseases. Being knowledgeable about current practices will help you stand out in discussions.
✨Tip Number 3
Network with professionals in the pharmaceutical industry who have experience in safety surveillance. They can provide insights and potentially refer you to opportunities within their organizations.
✨Tip Number 4
Prepare to discuss your experience with regulatory submissions in detail. Be ready to share specific examples of how you've contributed to successful submissions, as this is a key requirement for the role.
We think you need these skills to ace Global Safety Physician
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Global Safety Physician position. Understand the key responsibilities and requirements, especially focusing on safety surveillance and regulatory submissions.
Highlight Relevant Experience: In your CV and cover letter, emphasize your medical degree, clinical experience, and any specific work you've done in pharmacovigilance or rare diseases. Use concrete examples to demonstrate your sound medical judgment.
Tailor Your Application: Customize your application materials to reflect the language and priorities mentioned in the job description. Show how your background aligns with the company's focus on safety and risk management in rare diseases.
Proofread and Submit: Before submitting your application, carefully proofread all documents for clarity and professionalism. Ensure that your application is complete and accurately reflects your qualifications.
How to prepare for a job interview at BioTalent
✨Showcase Your Clinical Experience
Be prepared to discuss your medical degree and any relevant clinical experience. Highlight specific cases or projects where you demonstrated sound medical judgment, especially in the context of rare diseases.
✨Demonstrate Knowledge of Pharmacovigilance
Familiarize yourself with pharmacovigilance principles and be ready to explain how you've applied them in previous roles. Discuss any experience you have with safety surveillance and integrated safety data assessment.
✨Understand Regulatory Processes
Since this role involves regulatory submissions, brush up on your knowledge of FDA and EMA processes. Be prepared to discuss your experience with regulatory agencies and how it relates to safety and risk management.
✨Collaborate Effectively
This position requires collaboration with cross-functional teams. Think of examples where you've successfully worked with diverse groups to achieve safety standards. Emphasize your communication skills and ability to represent safety in decision-making forums.
