... oversee and support all contacts to external experts, executive steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience ...
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... oversee and support all contacts to external experts, executive steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience ...
de.talent.com
... , contractual agreements, and clinical data dissemination. Oversee individual trials, ... to regulatory submissions and clinical strategies. Work Environment : Regular travel ... international conferences and clinical site visits. Career Development : This ...
de.talent.com
... high quality investigative sites to support the client’s clinical development programs Collaborate with internal ... high quality investigative sites to support the client’s clinical development programs Responsible for the ...
de.talent.com
... fit someone who has previous clinical research experience or perhaps a ... of a study Provide ongoing support of sites, including identifying and ... site Qualification Visits, prepping consultation support for site audits, etc. Qualifications ...
de.talent.com
... for the delivery of all clinical aspects of the study Oversee the clinical portion of the budget, develops ... years related experience in (conducting) clinical studies 4 year degree or ... wellbeing initiatives are tailored to support you and your family at ...
de.talent.com
... and academic skills in clinical project administration and management. A ... an accelerated career path into Clinical Trial Management (CTM). Responsibilities Communicate ... specific status reports within the clinical trial management system Interact with ...
de.talent.com
... and academic skills in clinical project administration and management. A ... an accelerated career path into Clinical Trial Management (CTM). Responsibilities Communicate ... specific status reports within the clinical trial management system Interact with ...
de.talent.com
... pharmacovigilance issues. Per the Clinical Monitoring Plan (CMP) or SMP: ... external facilities, equipment, and supplies (clinical and non-clinical) continue to be adequate to ... clinic. Who are Parexel? Parexel supports clinical studies across the full range ...
de.talent.com
... close-out visits for clinical trials. Ensuring protocol compliance, data ... of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations, and ICH- ... who are there to support you and your family’s well- ...
de.talent.com