We are currently seeking a Clinical Study Associate, Sr... reporting, clinical data flow, site monitoring, and site close-out; Ensure the validity of the clinical...

that clinical personnel across the Medtronic Clinical... an advisor on clinical quality assurance issues regarding various aspects of the clinical study phases (e...

Develop clinical study documentation such as case report forms, informed consents, clinical study logs... clinical protocols for phase I – IV clinical studies;...

clinical study. Internally interfaces with data management, biostatistics, regulatory, clinical research associates, trial coordinators, field clinical monitors...

clinical investigations and execute through collaboration with key stakeholders to meet the clinical... Clinical Study · Developing study results · Clinical...

contribute outstanding clinical insight with consumer... Previous on-site clinical monitoring experience at a CRO is required 3+ years on-site clinical monitoring...

contribute outstanding clinical insight with consumer... Previous on-site clinical monitoring experience at a CRO is required 5+ years on-site clinical monitoring...

management support Variety of clinical trial projects... Clinical Research Associates manage all aspects of site monitoring responsibilities for Clinical trials...

Clinical Research Scientist for their new products division. This position completes NDA and ANDA clinical... clinical development plans and provide clinical...

resources to the Clinical Program Management group. The Director will ensure clinical projects/programs... with clinical development leadership and clinical...

clinical protocols for phase I - IV clinical studies;... and selection of CRO Partners involved in Clinical Development studies/projects and review clinical site...

connects clinical research professionals with opportunities to advance their careers.We currently have an exciting temporary opportunity for a Clinical Data...

printing of clinical study documents · Assembles and distributes clinical study materials Education and experience required: § 1+ year(s) clinical research...

relationships with clinical investigative sites for a... and summarization of clinical trials to ensure adherence to protocols, Good Clinical Practice (GCP), ICH...

device accountability for clinical sites • Assist Clinical Field Specialists and Clinical Research Manager in obtaining all necessary documents from clinical...

investigators and the clinical team • Assist Clinical Field Specialists and Clinical Research Manager in... Good Clinical Practice (GCP) training to clinical...

clinical trial study management with DaVita Clinical... Demonstrated understanding of clinical and regulatory components of clinical trial execution Demonstrated...

CRO) staff.Oversee the training of clinical... Act as Clinical Monitor when needed.Prepare final clinical reports.Support non sponsored clinical studies...

develop clinical study documentation such as case report forms, informed consents, clinical study logs... drafting and reviewing clinical protocols for phase I...

to customers. •Work with appropriate industry KOL and CRO to project value of Pfizer products. •Work... doctoral experience in clinical practice, academia...