Project assistant in Genomics, Diabetes and Endocrinology - Hiring in process/Finished, not possible to apply

Work duties

The candidate will be responsible for drafting and reviewing clinical study documentation, including: clinical protocols, reports and other necessary regulatory documents. The candidate will be coordinating cross functional relationships with laboratory and clinical investigations, biological sampling and quality control of the data in the project in Sweden and Ukraine.

Qualifications

• The applicant should hold a relevant degree in medical or biomedical sciences, diabetes, or endocrinology. PhD degree is not mandatory.
• The applicant should have background from clinical medicine, and clinical laboratory experience, particularly histological analyses of samples from different tissues.
• The successful applicant must have experience in counseling, supervising of medical and biomedical personnel, writing scientific manuscripts and preferentially also assisting in grant applications.
• The experience in clinical protocols and laboratory documentations is preferable.
• The applicant must be motivated and responsible, and also have a great work capacity and enthusiasm for clinical research.
• Experience with international collaboration is an advantage.
• Experience in organizing conferences is preferable.
• The candidate must be fluent in written and oral English as well as written and oral Ukrainian.

Employment duration: 12 months.