Are you looking for new challenge in Clinical Trial Management? Could you already gain experience in Clinical Trial Management? Then apply here:
Responsibilities
- Leading, mentoring and developing the clinical trial organization at Hamilton Medical, fostering a collaborative and high-performance culture
- Providing guidance and support to team members on clinical trial processes, regulatory requirements and company policies
- Conducting regular performance reviews and developing training plans for team members
- Developing trial strategies and ensuring the successful execution of clinical studies from inception to completion
- Overseeing the planning, implementation, and management of clinical trial portfolio (mainly European and US trials), including protocol development, site selection, and patient recruitment
- Developing and managing trial portfolio budget, timelines, and resources
- Ensuring trials are conducted in alignment with our product innovation strategy, regulatory requirements, company SOPs and ethical standards in compliance with GCP, ISO 14155, MDR and other relevant regulations
- Monitoring regulatory requirement updates
- Liaising with regulatory authorities as needed
- Developing and updating SOPs related to clinical trial management
- Managing and developing the overall clinical data management: data collection, quality, and analysis processes to ensure data integrity and accuracy
- Preparing regular progress reports for senior management and regulatory bodies
- Ensuring timely and accurate reporting of adverse events and deviations
- Serving as the primary point of contact for investigators, study sites, and external vendors (e.g. CROs)
- Facilitating communication with other internal departments, including R&D, regulatory affairs, and clinical affairs
Your Profile
- Master’s degree in life sciences, engineering or a related field
- Minimum of 8 years of experience in clinical trial management within medical device industry, with at least 4 years in a leadership role
- Track record of successful talent recruitment and development
- In-depth knowledge of GCP, ISO 14155, and regulatory requirements (MDR) for medical devices
- Proven track record of managing clinical trials from initiation to completion
- People’s lead mentality, strong leadership, organizational, and communication skills
- Motivation to act as an architect of an effective and efficient CTM organization, interpreting this task as a challenge and attractive opportunity
- Ability to manage multiple projects and prioritize effectively
- Proficiency in clinical trial management software and clinical data management
- Certification in clinical research, PhD and FDA experience are a plus
Benefits
- A responsible position with interesting challenges
- A stimulating and friendly working environment
- Competitive remuneration and benefits
Contact
In case of any doubt on this vacancy (ref.: JN -072024-618814), please contact Judith Atgé Martin at +41 58 233 45 41.
About Us
Adecco is the market leader for staffing solutions in Switzerland and worldwide. Every day, our teams in our 50 locations throughout Switzerland ensure the best match between candidates and clients in various professional fields and industries. Adecco Switzerland is part of the Adecco Group, the world’s leading talent advisory and solutions company. We believe in making the future work for everyone, and every day enable more than 3.5 million careers. We skill, develop, and hire talent in 60 countries, enabling organisations to embrace the future of work.