Állam állások, munkák klinikai kutató kategóriában

• biológiai minták feldolgozása, adatgyűjtés és pontos adatbevitel
• megfigyelések, mérési eredmények és kísérleti körülmények dokumentálása
• oldatok, reagensek, médiumok, pufferoldatok előkészítése és szakszerű eltakarítása
• fogyóanyagok nyomon követése, rendelési igények jelzése

• részvétel sejttenyésztésben és sejtes munkában (passzálás, kezelések)
• fizikai erőnlétet igénylő feladatok elvégzése (munkaidő 30-35%-át teszi ki):
• folyékony nitrogén tartályok szállítása és töltése
• veszélyes hulladék összegyűjtése és szállítása és nyilvántartása a vonatkozó biztonsági előírások szerint

Develop and implement global market access strategies for the whole lifecycle to ensure optimal pricing, reimbursement, and patient access for the company's urology and hematology portfolio as well as upcoming innovations across key markets...

Global MSAT Quality Systems (QMS) SpecialistGlobal MSAT Quality Systems (QMS) Specialist (m/f/d) : Quality Systems/ GMP Operations/ QMS/ CAPA/ Change Control/ MSAT/ Engineering Operations/ Pharma/ Veeva Vault/ Quality Docs/ LMS/ EnglishProject:For our pharmaceutical customer based in Basel, we are...

(Associate) Bioanalytical Principal Investigator LBS (100%)Celerion is one of the world's leading bioanalytical contract research companies and has been supporting pharmaceutical and biotech companies around the world for more than 40 years. Celerion offers services for the approval of new drugs -...

(Associate) Bioanalytical Principal Investigator LBS (100%)Celerion is one of the world's leading bioanalytical contract research companies and has been supporting pharmaceutical and biotech companies around the world for more than 40 years. Celerion offers services for the approval of new drugs -...

Scientific oversight and coordination of preclinical and toxicology studies conducted in collaboration with CROs, academic partners, and scientific institutions - covering both GLP-regulated and exploratory/non‑GLP research...

CMC Program Lead (Biologics) -Try&Hire (a)As CMC Program Manager, you will play a key role in driving the Chemistry, Manufacturing, and Controls (CMC) strategy and execution for the company's lead biologic program. You will collaborate closely with external Contract Development & Manufacturing...

Senior R&D Project ManagerJoin a Team Advancing Precision Surgery Through Advanced ImagingSamanTree Medical is a privately held Belgian–Swiss medical device company dedicated to improving precision in surgery through innovative imaging solutions. Headquartered in Liège, Belgium, with R&D in...

• You are responsible for quality related topics like change control, deviations and/or complaints related to DS products at CMOs
• Define together with the CMO effective CAPAs and track the timely implementation

Clinical Research Nurse InternThe Nestlé Group is the world's largest food and beverage company with 92.6 billion Swiss Francs in sales in 2019. It is present in 187 countries around the world, has 403 factories and its 291'000 employees are committed to Nestlé's purpose of enhancing quality of...

Working independently in the areas of valve crimping, case management, pre-case planning, post-case management, 3 Mensio management, Therapy Awareness program management and clinical education programs...

Clinical Research Nurse InternThe Nestlé Group is the world's largest food and beverage company with 92.6 billion Swiss Francs in sales in 2019. It is present in 187 countries around the world, has 403 factories and its 291'000 employees are committed to Nestlé's purpose of enhancing quality of...

• Plan and Conduct GCP Audits: Develop a risk-based audit schedule covering all relevant areas, including investigator sites, vendors, and internal processes, to ensure adherence to GCP guidelines
• Oversee Corrective and Preventive Actions (CAPA) specific to GCP (internal or external)

• Strategic planning, execution, and oversight of international Phase I clinical trials in accordance with GCP/ICH-GCP guidelines, regulatory requirements (EMA/FDA), and internal SOPs
• Preparation, review, and approval of all relevant study documents in collaboration with external service providers

Unterstützung innerhalb der F&E-Abteilung/Einführung neuer Produkte (Neuproduktentwicklung und Innovation) und anderer geschäftskritischer und/oder umsatzfördernder Maßnahmen von der Planung bis zur Kommerzialisierung...

Koordination und technische Leitung interdisziplinärer Entwicklungsteams in Bezug auf das technische Management von Entwicklungsprojekten, Projektplänen, Ressourcenplänen und die Erfüllung von Designanforderungen zur Produktoptimierung...