At a Glance
- Tasks: Lead innovative studies for medical devices, OTC, and cosmetics safety and efficacy.
- Company: Join a top-tier Consumer Goods manufacturer focused on product innovation.
- Benefits: Enjoy competitive salary, flexible working options, and professional development opportunities.
- Other info: Opportunity to present findings at conferences and contribute to peer-reviewed publications.
- Why this job: Be at the forefront of product innovation while collaborating with diverse teams.
- Qualifications: BS, MS, or PhD in biological sciences with 8+ years of relevant experience.
The predicted salary is between 54000 - 84000 £ per year.
Blackfield Associates are supporting a leading Consumer Goods manufacturing organisaiton, who are seeking a strategic and hands-on Senior Manager, Global Clinical Affairs to lead medical device, OTC, and cosmetics safety and efficacy studies, including claims substantiation. This role is pivotal in designing and managing robust in vitro and clinical programs that meet regulatory requirements and drive product innovation.
What You’ll Do
- Partner with Product Development to create innovative, scientifically sound study strategies.
- Design and oversee safety and claims substantiation studies for diverse product categories.
- Collaborate cross-functionally with Regulatory, Legal, Marketing, and Quality teams to deliver compliant protocols and actionable study results.
- Build and expand internal and external networks with CROs, consultants, auditors, and investigators.
- Manage full study lifecycle: protocol development, budget, monitoring, data interpretation, and reporting.
- Present high-impact study results to inform timely business decisions.
What You Bring
- BS, MS, or PhD in a biological science (e.g., Toxicology, Pharmacology, Biology, Physiology, Biochemistry).
- 8+ years of in vitro and clinical testing experience in medical devices, OTC, or cosmetics.
- Proven ability to lead complex projects across multiple categories and geographies.
- Knowledge of MDR – CER/BER and medical device safety/efficacy testing (preferred).
- Strong communication, problem-solving, and organizational skills.
- Track record of conference presentations and peer-reviewed publications.
Manager Clinical Affairs in Maidstone employer: STR Group
At Blackfield Associates, we pride ourselves on being an exceptional employer, offering a dynamic work environment that fosters innovation and collaboration. Our commitment to employee growth is evident through our comprehensive training programmes and opportunities for advancement within the Consumer Goods sector. Located in a vibrant area, we provide a supportive culture that values diversity and encourages employees to make meaningful contributions to product safety and efficacy.
StudySmarter Expert Advice🤫
We think this is how you could land Manager Clinical Affairs in Maidstone
✨Tip Number 1
Network with professionals in the clinical affairs field, especially those who have experience in medical devices and cosmetics. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends and requirements in clinical studies.
✨Tip Number 2
Familiarise yourself with the latest regulations and guidelines related to medical device safety and efficacy testing. Understanding MDR – CER/BER will give you an edge and demonstrate your commitment to compliance and quality in your work.
✨Tip Number 3
Showcase your leadership skills by discussing any past experiences where you successfully managed complex projects. Highlight your ability to collaborate cross-functionally, as this is crucial for the role and will set you apart from other candidates.
✨Tip Number 4
Prepare to discuss your experience with study lifecycle management in detail. Be ready to provide examples of how you've developed protocols, managed budgets, and interpreted data, as these are key responsibilities for the position.
We think you need these skills to ace Manager Clinical Affairs in Maidstone
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights relevant experience in clinical affairs, particularly in medical devices, OTC, and cosmetics. Emphasise your leadership roles and any specific projects that align with the job description.
Craft a Compelling Cover Letter:Write a cover letter that showcases your passion for the role and the industry. Discuss your experience in designing and managing clinical studies, and how you can contribute to the company's goals.
Highlight Relevant Skills:In your application, clearly outline your skills related to regulatory compliance, project management, and cross-functional collaboration. Use specific examples to demonstrate your problem-solving abilities and communication skills.
Showcase Your Achievements:Include any notable achievements such as successful study outcomes, publications, or presentations at conferences. This will help illustrate your expertise and commitment to advancing product safety and efficacy.
How to prepare for a job interview at STR Group
✨Showcase Your Technical Expertise
Make sure to highlight your educational background and relevant experience in biological sciences. Be prepared to discuss specific projects you've led, particularly those involving safety and efficacy studies in medical devices or cosmetics.
✨Demonstrate Cross-Functional Collaboration
Since the role requires collaboration with various teams, come ready with examples of how you've successfully worked with Regulatory, Legal, Marketing, and Quality teams in the past. This will show your ability to navigate complex organisational structures.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills and project management capabilities. Think of scenarios where you had to manage a study lifecycle from protocol development to reporting, and be ready to explain your approach and outcomes.
✨Highlight Your Communication Skills
As presenting high-impact study results is crucial, practice articulating your findings clearly and concisely. You might want to prepare a brief presentation on a past project to demonstrate your ability to communicate complex information effectively.
