TRABAJO REGULATORY AFFAIRS ASSOCIATE STUDY

This position reports to the regulatory affairs lead singapore (medtech)...   responsibilities: the regulatory affairs associate manager (medtech) will be a...

Proven experience in leading regulatory policy shaping and discussions with regulatory authorities and the affiliated test labs... experienced in driving industry...

Awareness or regulatory affairs environment, eu-wide legal framework, and european authorities’ websites... profilewe are looking for a dynamic, capable, curious...

The associate director study leader, early oncology clinical is responsible for the delivery of clinical studies including quality, timelines, budgets, resources...

We are selecting to work regulatory affairs associate at laboratorios liconsa (chemo)... serves as regulatory representative to marketing, r&d teams and regulatory...

Description: we have an open position for a lead regulatory associate to join our regulatory unit within the clinical operations department...

 knowledge and experience of medical affairs led evidence generation and related regulations...  deep understanding of local regulatory policy and industry’s...

Irc - legal & regulatory affairs at eni, we are looking for a legal & regulatory affairs - department manager within plenitude iberia in lisbon...

Manages study supplies (isf, etc), drug supplies and drug accountability at study site... prepares study drug for destruction, if applicable... ensures timely collection/uploading...

Excellent knowledge of study execution, benefit risk management and regulatory affairs... in-depth knowledge of study methodology, study data reviews and analysis...

Assists in the preparation of study protocols and study execution... this is what you will do: the associate medical director provides input into a clinical study...

• direct the study team in the implementation of audits and regulatory inspections... typical accountabilities • provides operational expertise to the study team...

Prepare and provide input to clinical study reports (csrs) and clinical portions of regulatory documents (e... responsible for timely responses to investigational...

Clinical research associate (sr... collect and review regulatory documents as required... monitor activities at clinical study sites to assure adherence to gcp,...

Abiomed, part of johnson & johnson's medtech, is recruiting for a clinical research associate ii... trends in protocol compliance, enrollment, monitoring deviations...

Proven experience in regulatory writing, with a focus on european regulations... role overview: as a principal regulatory writer, you will play a pivotal role in...

Previous experience with regulatory submissions... collaborators, key opinion leaders (kols), investigators, regulatory authorities, etc... ability to travel...

Experience writing epidemiology protocols and study reports is required... experience using healthcare databases, registries, observational study design is required...

Represent us affairs in various interactions with the global functions including clinical r&d, translational medicine, regulatory affairs/labelling, and global...