Meet our expert Anna Junell

With over 20 years’ experience from both the pharmaceutical industry and academic research, and with a strong background in clinical development, Anna guides clients through their development phases. “My experience, in combination with my knowledge of regulatory requirements and study design allows our clients to reach their goals on time and with a high quality delivery”.

Prior to joining SDS, Anna was an acknowledged Senior Clinical Research Associate (SrCRA) and Subject Matter Expert (SME) in Site Monitoring with expert knowledge in Good Clinical Practice. She has been leading trials as a local and regional Project Manager in both global and regional study setups.

“I have extensive experience managing complex phase I-IV clinical trials from feasibility and start-up to close-out phase in therapy areas as diverse as oncology, inflammation, vaccine, infection, haemophilia, urology, paediatrics and CNS. Typical assignments involve support of a timely start-up, protocol design, medical writing, regulatory submissions and study sponsor oversight, as well as coordination of other expert functions.”