Medical writer (freelance)

Profil Foto
Verfügbarkeit einsehen
  auf Anfrage
zh  |  en  |  de
  auf Anfrage
  79258 Hartheim (Breisgau)
 05.06.2018

Kurzvorstellung

I am a pharmacist by training, and I am a master in drug sciences. I have comprehensive knowledge in clinical pharmacotherapy and drug development, and years of experience in medical affairs in big pharmaceutical company.

Ich biete

Design, Kunst, Medien
  • Medical Writing
    2 Jahre, 2 Monate Erfahrung

Fokus
  • clinical research

Projekt‐ & Berufserfahrung

Medical Writer (freelance)
Kundenname anonymisiert, Hartheim am Rhein
6/2016 – offen (2 Jahre, 3 Monate)
Life Sciences
Tätigkeitszeitraum

6/2016 – offen

Tätigkeitsbeschreibung

Experienced Medical Writer in pharmaceutical medical/ marketing article composition. Diverse writing experience including disease or product summary report/ highlight/ flyer, presenter slides, training slides, advisor board meeting minutes, clinical trial documents, or customized materials. Solid clinical pharmacy knowledge in various therapeutic areas from professional pharmacist training in Taiwan and the US as well as solid knowledge in drug science from comprehensive education in University of Basel.
Hands-on experience of pharma-healthcare professional (HCP) interaction from years of experience in medical affairs of big pharma.

Eingesetzte Qualifikationen

Medical Writing

Zertifikate

Good clinical practice (GCP)
Januar 2017

Pharmacist license
Oktober 2011

Ausbildung

MSc of Drug Sciences
(Ausbildung)
Jahr: 2018
Ort: Basel

BSc of pharmacy
(Ausbildung)
Jahr: 2011
Ort: Taiwan

Qualifikationen

My name is Tsai-sang (Susan) [...]. I am a pharmacist by training, and I am a master in drug sciences. I have comprehensive knowledge in clinical pharmacotherapy and drug development. I have years of experience in medical affairs in big pharmaceutical company, and I have been working as a medical writer with diverse writing experience in variable pharmaceutical documents, including clinical trial-related documents (eg. study protocol, case-report form, inform consent form, and variable required documents for ethical committee submission.) as well as medical/ marketing-related documents such as flyers, advisory board slides, education slides, etc.
As a medical science liaison, I used to read and communicate clinical trial data with physicians, healthcare professionals, commercial colleagues, clinical research scientists, and other internal/ external stakeholders. Accordingly, I have great understanding in clinical trials, the operation, and the related documents. I also worked closely with clinical research team in Taiwan to facilitate them with site evaluation, initiation and study monitoring. For investigator-initiated trials (IITs), I was the key person in charge of trial master file (TMF) organization.

Über mich

I am currently looking for a position primarily involved in clinical research, so I can have more hands-on experience and more insights in the operation.

Persönliche Daten

Sprache
  • Chinesisch (Muttersprache)
  • Englisch (Fließend)
  • Deutsch (Grundkenntnisse)
Reisebereitschaft
auf Anfrage
Arbeitserlaubnis
  • Europäische Union
  • Schweiz
Profilaufrufe
27
Alter
29
Berufserfahrung
4 Jahre und 11 Monate (seit 09/2013)

Kontaktdaten

Nur registrierte PREMIUM-Mitglieder von freelance.de können Kontaktdaten einsehen.

Jetzt Mitglied werden »