Medical Advisor | Final Medical Signatory

Medical Advisor | Final Medical Signatory

Full-Time 36000 - 60000 £ / year (est.) On-site
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At a Glance

  • Tasks: Provide medical expertise and collaborate on innovative therapy strategies.
  • Company: Proclinical, a leader in the pharmaceutical industry with a focus on innovation.
  • Benefits: Competitive salary, professional development, and opportunities to impact patient outcomes.
  • Other info: Exciting role with excellent career growth and collaboration opportunities.
  • Why this job: Join a dynamic team and contribute to groundbreaking medical advancements.
  • Qualifications: 5+ years in Medical Affairs and strong communication skills required.

The predicted salary is between 36000 - 60000 £ per year.

Proclinical is seeking a Medical Advisor / Disease Area Specialist to join the Medical Affairs team. This role focuses on providing medical expertise across the innovative medicines portfolio, supporting therapy area strategies, and fostering collaboration with internal and external stakeholders. You will also contribute to new product planning and late-stage portfolio management, ensuring alignment with business objectives and compliance standards.

Key Responsibilities

  • Provide scientific and clinical input for designated therapy areas.
  • Collaborate with cross-functional teams to develop robust therapy area strategies.
  • Drive content creation and execute UK medical strategies and research plans for products and pipeline.
  • Act as a medical signatory, ensuring compliance with relevant codes and procedures.
  • Build and maintain partnerships with internal and external stakeholders.
  • Oversee portfolio tasks, prioritizing based on brand team needs.
  • Coordinate efforts between brand teams and field medical teams to align with brand strategies.
  • Lead medical assessments for early-stage assets to inform launch and commercialization decisions.
  • Partner with cross-functional teams to critically assess information and provide recommendations for asset development.
  • Act as the primary medical lead for Health Technology Assessments (HTAs), ensuring expert input and stakeholder engagement.
  • Provide medical expertise for non-promoted and late-stage portfolio assets, including sensitivity assessments and communication reviews.
  • Collaborate with commercial, market access, regulatory, and supply chain teams to manage asset lifecycle decisions.

Key Skills & Requirements

  • 5+ Years Medical Affairs Experience in Pharma
  • ABPI Final Medical Signatory - Essential
  • End-to-End Product Lifecycle Management Experience (Early, Mid & Late)
  • Product Strategy Development & Launch Experience
  • Advanced scientific or clinical degree; registered physician or UK-registered pharmacist preferred but not required.
  • Strong scientific understanding with the ability to quickly learn new therapeutic areas.
  • Experience in medical affairs, including product lifecycle management and strategy development.
  • Knowledge of the UK healthcare environment and compliance with the UK Code of Practice.
  • Excellent communication, presentation, and matrix team leadership skills.
  • Proven ability to prioritize tasks, assess risks, and adapt to changing circumstances.
  • Passion for improving patient outcomes and advancing scientific innovation.
  • Proficiency in Office business applications and familiarity with health technology assessments.

If you are having difficulty in applying or if you have any questions, please contact Josh Bye at j.bye@proclinical.com.

Medical Advisor | Final Medical Signatory employer: Proclinical Staffing

Proclinical Staffing is an excellent employer, offering a dynamic work environment in Barnard Castle where innovation meets quality. Employees benefit from a strong focus on professional development, with opportunities for growth within the quality control team, while enjoying a collaborative culture that prioritises adherence to GMP standards and excellence in microbiological testing.

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Contact Details:

Proclinical Staffing Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Medical Advisor | Final Medical Signatory

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Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Proclinical Staffing. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.

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We think you need these skills to ace Medical Advisor | Final Medical Signatory

Medical Affairs Experience
Final Medical Signatory
End-to-End Product Lifecycle Management
Product Strategy Development
Advanced Scientific or Clinical Degree
Strong Scientific Understanding
Knowledge of UK Healthcare Environment

Some tips for your application 🫡

Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Proclinical Staffing!

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How to prepare for a job interview at Proclinical Staffing

✨Understand the Science

Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Proclinical Staffing that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.

✨Showcase Relevant Experience

If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.

✨Know Their Products

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In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.