Job Overview:
This role involves leading and managing clinical research projects in the medical device industry. The ideal candidate will have experience in pre-market and post-market studies, as well as strong organisational skills.
The successful applicant will be responsible for designing, planning, implementing, and monitoring clinical research projects to ensure compliance with protocols and overall clinical objectives.
Key Responsibilities:
* Assisting interdisciplinary teams with project management
* Developing study-specific documents and preparing ethics submissions
* Maintaining trial master files and presenting at investigator meetings
* Collaborating with cross-functional teams to achieve project objectives
Requirements:
Bachelor's degree in Science or related discipline with 3+ years of experience in the medical device industry.
Experience in clinical research and project management is essential, with a strong understanding of regulatory requirements.
Excellent communication and problem-solving skills are also required, along with the ability to work independently and manage multiple priorities.
Benefits:
Working in a dynamic and innovative company with a team-oriented environment
Opportunities for professional growth and development
A competitive salary package with excellent benefits