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