Anna Uddén, MSc, Senior Clinical Project Manager

Ms. Anna Uddén joined Sigrid Therapeutics in January 2019.

Ms. Uddén is an experienced clinical trials specialist. She has a combined 27 years’ experience working in the pharma industry including 16 years as a Project Manager, 12 years’ experience in managing global studies and 7 years’ experience in line management.

Her extensive clinical trials experience has resulted from positions within both CRO and big pharma, most recently at Swedish Orphan Biovitrum, where, as Clinical Study Manager, she lead and managed the cross-functional global clinical team in Rare diseases.

Prior to this, Ms. Uddén was a Senior Project Manager at PRA Health Sciences, where she was responsible for management of full service global clinical trials within Hepatitis B and Epilepsy.

Jan 2019-current Clinical Study Manager, Sigrid Therapeutics
2017- Jan 2019 Clinical Study Manager/Leader, Swedish Orphan Biovitrum, Stockholm
2013-2017 Senior Project Manager, PRA Health Sciences
2005-2013 Project Manager/Senior Project Manager/Line Manager, ICON Clinical Research
2003-2005 Affiliate innovator, Medical IT, Eli Lilly AB
1995-2003 Clinical Trial Operation Manager/Project Manager, Roche AB
1994-1995 Clinical Research Associate, Eli Lilly AB
1991-1994 Product Manager, ASTA Medical AB

Education

1991, MSc., Biology and Toxicology, Uppsala University, Sweden
1991-1993, IHM business school for Pharmaceutical Companies

Läkemedelsakademin (Apotekarsocieteten): Basics in Clinical Trials; Planning; Protocol writing; CRF’s; Agreements and contracts in Clinical Trials; Statistics planning and analysis of Clinical Trials; GCP in Clinical Trials
2002, Vendator: Project Management