Patient Development Jobs in Lausanne
Debiopharm - Lausanne, VD
Development of clinical and regulatory documents such as Clinical Trial Protocols, ICFs, CSRs, IBs, and other clinical documents; with the aim to deliver accurate documents, suited for the intended audience...
von: workable.com (+1 Quelle) - Vor 2 Tagen
LHH - Lausanne, VD, CH
Take a broader organizational view of account management, with a focus on patient pathways optimization and market development. Work closely with diverse functions to meet customer demand. Our client is...
von: monster.ch - Vor 9 Tagen
Debiopharm - Lausanne, VD
Collaborate with cross-functional teams, including clinical operations, Clinical Development, regulatory affairs, and data management, to ensure the successful implementation of clinical trial protocols...
von: workable.com (+1 Quelle) - Vor 17 Tagen
Debiopharm - Lausanne, VD
Set up and maintain accurate trial information in tracking systems and communication tools for updating the relevant internal/external boards (e.g., Core Team, Development Leadership Team, and Core Team)...
von: workable.com (+1 Quelle) - Vor 17 Tagen
Lausanne, Waadt, Switzerland
In depth experience with design, conduct, analysis, interpretation and reporting of randomized clinical trials (RCTs) and adaptive designs for rare disease, ideally in the regulated environment of “orphan...
von: jobleads.de - Vor mehr als 30 Tagen
Debiopharm - Lausanne, VD
The use of external staffing agencies or recruiters requires prior approval from our Human Resources Department. The Human Resources Department at Debiopharm requests external staffing agencies or recruiters...
von: workable.com - Vor mehr als 30 Tagen
Debiopharm - Lausanne, VD
Lead control strategies for DS and DP, taking into consideration the status of the project, assessing risks, and ensuring their mitigation: define specification and justification thereof, lead the analytical...
von: workable.com - Vor mehr als 30 Tagen
RegenLab SA - Le Mont-sur-Lausanne
If you are passionate about regulatory affairs and thrive in a fast-paced and dynamic environment, we invite you to join our team and be part of our mission to improve healthcare worldwide. Apply now by...
von: jobscout24.ch - Vor 24 Tagen
Debiopharm - Lausanne, VD
Develop a “risk-based” compound-specific compliance program contributing to document / data accuracy, ultimately resulting in “dossier acceptability” by respective out-licensing partners (emphasis on eCTD...
von: workable.com - Vor mehr als 30 Tagen
Dentsply Sirona - Ballaigues
3-5 years’ experience within international multi-disciplinary R&D or QA/RA organizations in the area of medical device design control and regulations (21 CFR part 820, 93/42/EC Directive, 2017/745 EU Regulation...
von: jobscout24.ch - Vor 15 Tagen