Requistion ID : 75945

　　Dentsply Sirona is the world’s largest manufacturer of professional dental products and technologies, with a 130-year history of innovation and service to the dental industry and patients worldwide. Dentsply Sirona develops, manufactures, and markets a comprehensive solutions offering including dental and oral health products as well as other consumable medical devices under a strong portfolio of world class brands. Dentsply Sirona’s products provide innovative, high-quality and effective solutions to advance patient care and deliver better and safer dentistry. Dentsply Sirona’s global headquarters is located in Charlotte, North Carolina, USA. The company’s shares are listed in the United States on NASDAQ under the symbol XRAY.

　　Bringing out the best in people

　　As advanced as dentistry is today, we are dedicated to making it even better. Our people have a passion for innovation and are committed to applying it to improve dental care. We live and breathe high performance, working as one global team, bringing out the best in each other for the benefit of dental patients, and the professionals who serve them. If you want to grow and develop as a part of a team that is shaping an industry, then we’re looking for the best to join us.

　　Clinical Research Manager

　　Do you want to work with clinical studies in a global environment? We are a dental company with products in the field of dentistry and what we do really makes a difference to people’s lives. We give people their smiles back, which is very rewarding being part of. The role will offer you a broad spectrum of tasks in an international environment and with many different contact settings. We take great pride in making sure our products are safe and compliant and our clinical studies are a crucial factor in this work. Our company has a long history and we have a constant drive towards being in the forefront of what we do.

　　Come and join our engaged Clinical Research team!

　　Center of Clinical Research at Dentsply Sirona is responsible for the planning and performance of all phases of our clinical studies. This can be sponsored studies on non-approved products as well as on regulatory approved and marketed products. In this role you will be responsible for the preparation of the required study documents, including time plans and study agreements. You will work in close collaboration with other departments within Dentsply Sirona, as well as with dental clinics and universities worldwide. The role will offer you great insight to clinical studies in a global context and you will be part of many interesting projects along the way.

　　Responsibilities

　　Planning and execution of clinical studies according to applicable regulations

　　Preparation of study documents such as study protocol and study agreement

　　Preparation and submission of clinical investigation documentation to Independent Ethics Committees/Review Boards and Regulatory Authorities

　　Registration of clinical studies in applicable databases

　　Monitoring – up to 20 travel days are expected

　　Data management and follow up on time plan and budget

　　Study data analysis, preparation of clinical investigation reports and presentation of study data to internal and external parties

　　Qualifications / Background

　　Higher education in natural science

　　Background in dentistry, research and/or clinical studies

　　Experience working with Medical devices is preferable

　　Knowledge of Medical Device regulations related to conduct of human clinical studies (e.g. ISO 14155, MDR, FDA, GDPR, Declaration of Helsinki and Good Clinical Practise (GCP))

　　Fluent English in writing and speaking

　　The ability of being able to travel internationally

　　As a person you have a scientific mindset and you are market oriented. You will need to be structured, engaged and solution-oriented with a drive for result. Good collaboration skills are essential as well as strong communication.

　　The position will be located in Mölndal, Sweden and reports to the Director of Center of Clinical Research.

　　Please note that we will review applications continuously, so be sure to send in your CV as soon as possible.

　　Welcome with your application!