Clinical Research Associate
TFS, Sweden
Job Description
Through this exciting opportunity you have the chance to join a dermatology company in Uppsala as a Clinical Research Associate, being employed by TFS and fully outsourced to our client who has the whole product chain from research and development to production and marketing.
Our client is offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged.
The role includes:
• Compilation/review of clinical trial documents related to monitoring and site interactions (e.g. Clinical Trial Agreement, Clinical Study Protocol, Subject Information and Informed Consent forms, Monitoring Manual and other manuals, Newsletter, Investigator’s File)
• Review of submissions to ethics committee/health authorities
• CRF design and validation of database/e-CRF system
• Oversee study product and study material (order, label, shipping)
• Contact with CRO including training of CRO’s CRA
• Site/co-monitoring
• Study administration including archiving of study documentation
• Handling of clinical study data and participate in data / data base closure preparations
Requirements
Basic requirements:
- University degree in Biology, Pharmacy, or Medicine or similar
- 5-8 years of work experience
- Thorough knowledge in Good Clinical Practice
- Life Science experience
Wishful mindset:
- Courage and willingness to learn and work with new things
- Flexible to changes
We are conducting interviews on an ongoing basis so please apply today if you want to know more about this opportunity.