Project engineer Jobs in Lausanne
- Gesponsert
Clinical Project Manager
PharmiwebLausanne, CHBusiness Analyst / Business Engineer (m / f / d)
HaysLausanne- Gesponsert
Customer Project Manager Integrated Photonics (ID 2421)
Ligentec SALausanne, Kanton Waadt, CHLead Frontend Engineer
LHHLausanne, Vaud, SwitzerlandPROJECT MANAGER F / M
DNP Photo Imaging EuropeLausanne, Vaud, CHProject Manager Engineering
ExpleoLausanne, VD, CHAssistant & Project Coordinator
IncyteMorges, Vaud, SwitzerlandSoftware Project Manager
microTECH Global LtdLausanne, SwitzerlandSenior Equipment Project Manager.
MedtronicTolochenaz, Vaud, Switzerland- Gesponsert
Product Project Manager (H / F)
Michael PageVaud, CH- Gesponsert
Project Procurement Manager 80-100 %
Siemens Schweiz AGRenens VD, CHQuality Engineer
LimulaLausanne, VD, CH- Gesponsert
Sheet Music Project Manager (Classically Trained)
Tomplay IncPully, Kanton Waadt, CHProject Manager
TalanLausanne, SwitzerlandCAPEX Project Manager
CapgeminiLausanne greater area, CH- Gesponsert
Software Test Engineer ISTQB ( foundation level ) - 80% – 100% full time -
Helvetica PartnersLausanne, CHSoftware Engineer
Oratek SAEcublens, Vaud, SwitzerlandEmbedded Software Development Engineer
Sensile Technologies SAMorgesEmbedded Software Development Engineer
WIKA PolskaMorgesElectromagnetic Engineer
H.GLASSEcublens, Lausanne, CHClinical Project Manager
PharmiwebLausanne, CHJob Title : Clinical Project Manager – Vaccines
Location : Switzerland
Company Overview : Join a leading biotechnology company at the forefront of vaccine development, dedicated to improving global health through innovative solutions.
Position Overview : The Clinical Project Manager (CPM) will oversee the planning, execution, and completion of clinical trials for vaccine candidates. This role ensures that studies are conducted in compliance with ICH-GCP guidelines, regulatory requirements, and company standards.
Key Responsibilities :
- Project Leadership : Lead cross-functional teams to deliver clinical trials on time and within budget.
- Study Planning and Execution : Develop comprehensive project plans, including timelines, budgets, and resource allocation. Oversee study start-up, conduct, and close-out activities.
- Vendor Management : Select and manage Contract Research Organizations (CROs) and other external vendors to ensure quality and compliance.
- Regulatory Compliance : Ensure all clinical trials adhere to ICH-GCP guidelines, local regulatory requirements, and company Standard Operating Procedures (SOPs).
- Risk Management : Identify potential risks and develop mitigation strategies to ensure successful study outcomes.
- Budget Management : Monitor and control study budgets, ensuring financial objectives are met.
- Communication : Serve as the primary point of contact for internal stakeholders, study sites, and external partners.
- Documentation : Oversee the maintenance of the Trial Master File (TMF) and ensure all study documentation is accurate and up-to-date.
Qualifications :
Skills :
Benefits :
Application Process : Interested candidates are invited to submit their resume and a cover letter detailing their relevant experience and motivation for applying.
Join us in our mission to develop ground-breaking vaccines that make a difference in global health.