Klinikai kutató állások, munkák

• 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

• A klinikai adatokat és mellékhatásokat tartalmazó esetek átvétele különböző forrásokból.
• Az európai, holland nyelvű dokumentumok angolra történő fordítása és az információk pontos adatbázisba történő bevitele.

• 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

R & D FORMULATION SCIENTIST (12-month temporary mission)An innovative pharmaceutical laboratory active in pharmacy and biotechnology domainsreinforces its team and is hiring aR & D FORMULATION SCIENTIST (12-month temporary mission)TRB Chemedica is an international pharmaceutical company,...

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...

QA Manager - Drug Product klinische HerstellungQA Manager - Drug Product Clinical Manufacturing (m/f/d) - Quality Assurance / Pharmaceutical / cGMP / Synthetic Molecules / GMP Audits / SAP / Veeva / German / EnglishProject: For our client, a large pharmaceutical company based in Basel, we are...

Clinical ManagerAbout the role:Acrostak is a global leader in health technology, committed to improving hundreds of thousands of lives worldwide and striving to make the world healthier and more sustainable through optimized manufacturing and innovation.We are looking for a Clinical Manager, which...

• Planning, writing, reviewing and submitting manuscripts on clinical drug trials in humans for peer-reviewed journals and abstracts for scientific conferences
• Data visualization of data from clinical drug trials
• Supporting preparation of posters and conference presentations

• Develop clinical trial strategies, shaping study designs based on regulatory requirements, competitive insights and company's research interest.
• Give insights into clinical data sets and evidence for our company's products to internal stakeholders.

(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 -...

• Drive and complete reimbursement applications for the Vibrant product portfolio
• Build and check health economic models that clearly demonstrate product value by using appropriate software tools

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...

Scientist Quality Assurance (100%)INNOMEDICA IS A YOUNG NANOTECH COMPANY with around 40 employees, several promising drugs in preclinical and clinical development and its own clean room production. The pipeline is based on a liposomal delivery system and includes, in particular, parenteral drug...

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...

Active contribution to international projects in the areas of reimbursement and market access, including coordination, analysis, and substantive input on strategic topics...

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...

• 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...

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...