As a consultant within Clinical Development, you are contributing with operational and strategic support to SDS Life Science’s clients with preparation, implementation, and reporting of clinical trials of a drug or medical device. You are an important part in our contact with sponsoring companies, CRO, and testers, as well as interaction with governmental authorities. You will also have an important role in developing Clinical Development as a business area within SDS Life Science.
The employment is permanent, with starting date according to our agreement. You will be employed by SDS Life Science in Danderyd, Stockholm, where we offer a happy and productive atmosphere and, considering the times we are in, we also offer a work environment suited for distance work. We offer beneficial terms of employment and part-time work (80%) can be discussed.
- At least five years of work experience in clinical trials/studies.
- We prefer if you have experience in working independently at a smaller pharmaceutical- or biotech company/CRO
- Experience from leading the entire, or parts of a project/studies, as well as medical writing of study protocol or study reports.
- Academic degree within the natural sciences, healthcare
- Professional level of spoken and written Swedish and English
We think that you, as an important part of SDS Life Science culture and development, are goal-oriented, communicative, and like to explore new possibilities with others.
We look forward to your application!
Application and contact
For more information, call Maria Wanderoy, 070-5706593. Email your application to firstname.lastname@example.org as soon as possible. Write ‘’Senior Clinical Project Management in the title/subject line of the email . Interviews will be kept ongoingly.
About SDS Life Science
SDS Life Science is a Swedish consulting company that focuses on regulatory and scientific expertise within product development of drugs and medical technology, biostatistics. Our most important asset is our work force, where everyone have long experience in drug development in the pharmaceutical industry, governmental authorities and/or academic research. Hence, we can offer our client a unique concept consisting of cutting-edge competence and the over all responsibility of some parts of a project, or the entire project itself.