LAVORO START UP CLINICAL TRIAL

clinical trial management and central trial oversight services provide for the regional/global coordination of clinical trial management activities for internally...

clinical trial manager (ctm)/global trial lead (gtl), local management/country head and other study team members, as required... support clinical trial manager,...

The clinical trials assistant (cta) is responsible for project-supporting clinical drug research and development tasks... the cta will provide administrative and...

The clinical trial coordinator is responsible for start up activities and documents management... good knowledge of clinical research and regulatory/ethical requirements...

Responsibilities: to review etmf plans to upload documents in the etmf and perform ongoing quality control of the etmf (investigational products and clinical trial...

Solid knowledge of clinical data management and... to upload documents in the etmf and perform ongoing quality control of the etmf (investigational products and...

Experience and skills: required: minimum of 2 years of clinical trial management experience or a total of at least 5 years of clinical trial monitoring and/or clinical...

Maintains and updates trial management systems... an associate, local trial manager is an entry level trial management role... this role is responsible for local...

Site management); develops clinical trial documents (e... this clinical research leader will be responsible for leading and supporting one or several clinical trials...

Our j&j medtech neurovascular clinical team is currently seeking a senior clinical research specialist... site management) ability to serve as the primary contact...

Description our j&j medtech neurovascular clinical team is currently recruiting for a clinical research manager... clinical project leadership across multiple studies/...

Site management); contribute towards development of clinical trial documents (e... overview this senior clinical research specialist will be responsible for supporting...

clinical research certification (acrp or socra, clinical coordinator/cra certification) preferred... ability to travel up to 65% required... conduct reviews of documentation...

They are looking for a clinical affairs program manager europe... overall responsibility for design of clinical trials including protocol development, clinical trial...

Set up trial sites, ensuring that each center has the necessary trial materials... document accountability, stability, and storage conditions of clinical trial materials...

Provide oversight of and insight into trial activities (e... employees are eligible for the following time off benefits: vacation – up to 120 hours per calendar...

General description: accountable for regional study delivery with appropriate inspection readiness quality, within agreed timelines and budget leads the regional...

clinical research associate (sr... requirements to be successful you will possess: at least three years clinical monitoring experience and/or relevant clinical trial...

In-depth knowledge of clinical trials and the critical elements for success in clinical trials... may prepare regulatory and ethics committee submissions working...

Provides general support to the clinical research division on quality control of clinical data... skills: cardiology, oncology, respiratory, clinical research associate...