Associate Medical Director
Bracknell
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.
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Recruiter: Manpower UK
Salary: £60 to £70 Per Hour
Reference: BBBH433384