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Pharmaceutical Development Scientist / Technical Writer

Oxford Global Resources - Nijmegen
We are looking for a Pharmaceutical Development Scientist / Technical Writer. Your responsibility will be to optimize and validate manufacturing processes for pharmaceutical compounds intended for clinical trials. This
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Administrative Support (Patient Safety)

Oxford Global Resources - Breda
Programs, Clinical Trials and spontaneous reports. Responsibilities PSPs are homecare programs where third-party nurses go to patients' home to explain the use of the products and in some cases administer the product to the patient
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Clinical Study Lead

Derks & Derks B. V. - Utrecht
Offer working at a quality-oriented biopharmaceutical company a challenging job with a lot of responsibilities Position As a Clinical Study Lead you
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Translation of heeft een in English

Reverso - Amsterdam
hear PatrolTec has an opening . has an opening Functieomschrijving Yacht Life Sciences heeft een vacature voor... Functieomschrijving Yacht Life Sciences has a vacancy for a Clinical Study Associate. has a
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Country Safety Head FR/EN (part-time - 5 FTE)

Oxfordcorp
Manager to ensure adequate resources and budget are allocated and builds close and robust relations/collaboration with the in-country partner functions, including but not limited to Medical, Regulatory, Quality, Commercial, Legal
 60+ dagen geleden - Preview

Onderzoeksarts Principal Investigator binnen het kli...

DoctorConnect - Groningen
uit van een projectteam bestaande uit o.a. een Project manager , Apotheker, Clinical Study Manager en een Data Manager . Samen zorgen jullie er voor dat het onderzoek goed opgezet en uitgevoerd wordt, en dat de
FULL_TIME

Study Start Up Associate I - Dutch Speaker

Icon Plc - Utrecht
mission to shape the future of clinical development. We are currently seeking a Study Start Up Associate I to join our diverse and dynamic team. As a Study Start Up Associate II at ICON, you will play a pivotal role in leading
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Study Start Up Associate I - Dutch Speaker

Icon Plc - Utrecht
Job Categories Study Start Up Job Type Permanent Description As a Lead Site Activation Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare
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CRA II in ICON

Icon Plc - Amsterdam
coutnry regulations, sponsor policies, quality standards and adverse event reporting requirements. Acts as primary site contact and site manager throughout all phases of a clinical research study , taking overall responsibility

Assistent-manager

Reverso - Sint Maarten
employee. vacancy for Functieomschrijving Yacht Life Sciences heeft een vacature voor ... Functieomschrijving Yacht Life Sciences has a vacancy for a Clinical Study Associate. vacancy for Er was een vacature voor

Country Safety Head (EN FR)

Oxfordcorp
study protocols Requirements Life Sciences background Minimum 3 years of pharmacovigilance/ clinical development experience in Belgium Experience with pharmacovigilance systems and safety related product management in
 60+ dagen geleden - Preview

Ontmoet ons team

Novartis
zo waardevol maakt? Lees zijn verhaal → Nine van Zadelhoff Clinical Study Manager “Ik ben verantwoordelijk voor een goed verloop van de studies in de ziekenhuizen die onze projectteams vanuit Novartis begeleiden
 60+ dagen geleden - Preview

QA Technology Manager

Derksenderks via Monster Worldwide - Leiden
cycle reviews. You assure the completeness of the Product Specification File and the Study File to facilitate certification of clinical trial materials by the Qualified Person. As QA Manager you participate and contribute to
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