TRABAJO CLINICAL STUDY MANAGER BARCELONA, BARCELONA

Typical accountabilities • provides operational expertise to the study team... location: barcelona, spain (on-site) role description the senior global study manager...

The global study manager is responsible for supporting the delivery of clinical studies ensuring quality and compliance... desirable early phase oncology clinical...

Provides matrix management of functional area representatives to cross functional clinical study teams... accountabilities: leads the delivery of the clinical study...

• experience in all phases of a clinical study lifecycle... • extensive knowledge of clinical research regulatory requirements (incl ich-gcp) and demonstrated abilities...

Coordinating with cpl and cross-functional team to assemble study documents as appendices for csr at study close-out... coordinating study team training in the investigator...

• early oncology clinical delivery... we are seeking a director study leader rtsm specialist in early oncology clinical (eoc)... • understanding of early phase clinical...

Gov/eudract and monitor its update throughout a study... you will need to have: 2 years of clinical research experience or course-work equivalent in clinical research...

We are looking for an clinical data and networks project manager to provide a unique platform for the extraction of clinical data from information systems (healthcare...

Training / strong knowledge on good clinical practices... experience: 2-3 years of experience in a clinical research management... extensive knowledge of all steps...

We want to be the clinical research organisation that delivers excellence to our clients and to patients at every touch-point... y ou will be adding value through...

Serve as the medical expert for clinical study team... assists in the preparation of study protocols and study execution... engage with clinical investigators on...

clinical input to nda/bla)... prepare and provide input to clinical study reports (csrs) and clinical portions of regulatory documents (e...

Lead and participate in activities that ensure quality, consistency and integration of clinical study related deliverables and ensure safety evaluation process within...

Typical responsibilities may include: •    provide long-range clinical planning in early clinical trial development, planning and managing of clinical research projects...

The clinical research medical advisor is a global clinical development role with medical responsibility for the clinical trial process...

study files, crfs, etc... study files, crf files, monitoring files, etc... log in, tracking, quality control as appropriate for the study   • *to share responsibility...

Regardless of the study type, key accountabilities include management of study governance processes, stakeholder management, finance management support, project...