Medical Writer Jobs
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Search Results - Medical Writer Jobs
AO Foundation-Zizers
and posters/presentations)
• Evaluate and interpret clinical data in collaboration with the medical subject matter experts (PCIs), medical biostatisticians, and medical writers
• Adverse Event Review as specifically defined in the CIP/RP for each clinical...
Debiopharm-Lausanne
working on innovative medicines for patients. Join our team at Debiopharm where together, we innovate, we impact, and we grow.
For our Clinical Development organization based at our Headquarters in Lausanne, we are looking for a
Medical Writer...
workable.com -
AO Foundation-Zizers
and posters/presentations) Evaluate and interpret clinical data in collaboration with the medical subject matter experts (PCIs), medical biostatisticians, and medical writers Adverse Event Review as specifically defined in the CIP/RP for each clinical research...
AO Foundation-Zizers
Maintain contact with principal investigators and study nurses
• Evaluate and interpret clinical data in collaboration with the statistician, the medical advisor and the medical writer
• Review interim and annual registry reports...
ostjob.ch-Zizers
documents (such as OnePager, CIP/RP, SAP, FSR, manuscripts, conference abstracts, and posters/presentations)
• Evaluate and interpret clinical data in collaboration with the medical subject matter experts (PCIs), medical biostatisticians, and medical writers...
jobup.ch -
Planet Pharma-Basel
Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably...
Audemars Piguet-Le Brassus
Technical Writer
Le présent et le futur d'Audemars Piguet se construisent grâce à la contribution de tous nos talents. Inspirés par la richesse de notre passé, nous sommes enthousiastes à l'idée de ce que nous créerons dans le futur. Ensemble, nous...
Stettler Consulting AG-Zurich
Veterinär-Präparate.
Ihre Aufgaben :
• Führung, Coaching und Weiterentwicklung des Regulatory- und Medical-Teams
• Aufteilung der Verantwortlichkeiten innerhalb der Abteilung Registrierung
• Erstellung und Optimierung von abteilungsrelevanten Abläufen...
Stettler Consulting AG-Zurich
Sie übernehmen die Abteilungsleitung zur regulatorischen Betreuung der Human- und Veterinär-Präparate. Ihre Aufgaben: Führung, Coaching und Weiterentwicklung des Regulatory- und Medical-Teams Aufteilung der Verantwortlichkeiten innerhalb der...
Medison group-Schweiz
Senior Medical Director, European Partner Markets
About The Position
Medison is a rapidly growing global pharmaceutical company with a strong global presence, operating in 4 continents and over 24 countries. Our mission is to provide access...
appcast.io -
Mirum Pharmaceuticals, Inc.-Basel
POSITION SUMMARY
The Senior Medical Director will join the Clinical Development group and will be responsible for all clinical trial related activities in all stages of clinical development in a cross-functional team of internal and external...
Medison group-Baar
Senior Medical Director, European Partner Markets
About The Position
Medison is a rapidly growing global pharmaceutical company with a strong global presence, operating in 4 continents and over 24 countries. Our mission is to provide access...
appcast.io -
CK Group-Schweiz
Company Core Data Sheet (CCDS) etc. Previous experience with safety signal identification methodology and risk minimization measures. Excellent medical writing skills. Good presentation skills. Excellent interpersonal, communication and negotiation skills...
Neurocrine Biosciences-Basel
knowledge of Excel
• Strong publication/medical writing experience is required
• Ability to synthesize, analyze and summarize data, think critically, manage projects, influence others
• Ability to work in a team environment, across multiple departments...
appcast.io -
Bien-Air Surgery SA-Bienne
At least 4 years' experience in clinical evaluations, medical writing or clinical research in the medical device sector.
• In-depth knowledge of national and international regulations applicable to medical devices (ISO 13485, MDR 2017/745, MDSAP, FDA, etc...
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