Associate Medical Director
| Posting date: | 19 February 2026 |
|---|---|
| Salary: | £61.31 per hour |
| Hours: | Full time |
| Closing date: | 05 March 2026 |
| Location: | Bracknell, Berkshire, rg12 8ht |
| Company: | Manpower UK Limited |
| Job type: | Temporary |
| Job reference: | BBBH433384_1771503759 |
Summary
Associate Medical Director
Join a leading innovator in the medical device industry, dedicated to improving patient outcomes through cutting-edge technology and scientific excellence. Our organisation prides itself on fostering a collaborative, dynamic environment where medical professionals can make a tangible impact on healthcare. With a commitment to continuous development and a focus on regulatory compliance, we offer an attractive and rewarding career path for experienced medical professionals seeking to contribute to meaningful advancements in medical devices.
Job Responsibilities
- Provide medical insights for product development, risk assessments, and customer interactions to ensure clinical relevance and safety.
- Oversee the design, execution, and analysis of clinical studies to support product approvals and post-market surveillance activities.
- Monitor safety data during clinical trials, assess adverse events, and ensure participant safety throughout the study life cycle.
- Contribute medical expertise during the introduction of new products, ensuring clinical validity and regulatory compliance.
- Provide medical input in complaint management processes to facilitate effective resolution and continuous improvement.
- Develop and maintain relationships with key opinion leaders and industry experts to gather insights and foster collaboration.
- Collaborate closely with R&D, Quality Assurance, Regulatory Affairs, and Marketing teams to align clinical objectives with business goals.
- Ensure all activities comply with relevant regulatory requirements and industry guidelines.
- Contribute to the training of medical and non-medical personnel to promote understanding of clinical and regulatory standards.
- Provide medical input for the development of marketing and educational materials to ensure scientific accuracy.
- Support the development and execution of medical education and scientific evidence strategies to enhance product credibility.
Required Skills & Qualifications
- Medical degree (MD or equivalent) with active registration preferred.
- Minimum of 5 years clinical experience, ideally within the medical device industry.
- Experience in medical affairs roles, with a strong understanding of clinical trial monitoring and medical device regulations.
- Proficiency in statistical principles, Good Clinical Practice (GCP), and other relevant regulations governing clinical research.
- Demonstrated ability to lead cross-functional teams and manage complex projects effectively.
- Excellent verbal and written communication skills, capable of conveying complex information clearly and professionally.
- Strong problem-solving skills with a data-driven decision-making approach.
- Knowledge of medical device regulatory landscape is desirable.
- Additional postgraduate qualifications in medicine, management, or related fields are advantageous.
- Proficiency in additional languages is a plus, enhancing communication with global stakeholders.
- Ability to thrive in a fast-paced, dynamic environment with adaptability and resilience.