Trine Birgitte Moulvad

Pharma developer eager to help with Regulatory hurdles.København, DanmarkUnique capabilities within drug development & regulatory strategic thinking and negotiation. Constructive & lean innovation mindset. Result oriented & data-driven. Bring enthusiasm and engagement to the table. Motivated by challenges. High capacity & integrity. Proven record of successful regulatory agency negotiations enabling efficient global drug approvals. Thrive building and developing functions/organisations. Good network. Have worked and lived in the UK and the US, culturally agile.

Bestyrelseserfaring

Ingen bestyrelseserfaring

Erhvervserfaring

2014 -

VP Regulatory, Pt Safety and Med.writing @ ZEALAND PHARMA A/S

2003 - 2015

VP, RA GLP-1 & Obesity @ NOVO NORDISK A/S

1998 - 2003

Sn.Dir. RA @ FERRING PHARMACEUTICALS A/S

1995 - 1999

RA Project Lead & Head of PV Case Mgmt @ Lilly Research Centre

Uddannelser & kurser

2005 - 2006

Diploma in “Managing Med. Product Innovation @ SIMI/CBS

1995 - 1997

PV Certificate @ Uni of Hertfordshire

1980 - 1989

MScPharm @ KU

Handlinger

Du kan kontakte denne kandidat, ved at sende en personlig besked.

Tilføj denne kandidat til dine favoritter.

Ekspertiseområder

Drug development and approvals

Sprog

Engelsk

Tysk