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 Randamp;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 andamp; 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.