- CSL Behring (King Of Prussia, PA)
- …market biotherapies used to treat serious and often rare conditions. Could you be our next Director Clinical Research ? This is a hybrid role located in our ... experience, with 1 including accountability for medical oversight/evaluation or clinical development. + Industry experience in designated therapeutic area(s). +… more
- CSL Behring (King Of Prussia, PA)
- …also be considered. + Extensive knowledge of the drug development process and clinical research methodologies including experience in clinical trial design, ... which includes accountability for medical oversight/evaluation or Phase 2b/3 clinical development experience. Relevant academic research experience will… more
- CSL Behring (King Of Prussia, PA)
- As a true expert in the responsible TA, the Executive Director , will lead the development and execution of Medical Affairs strategies and tactics in support of the ... that accurate and robust TA/product related medical-scientific knowledge and clinical expertise, is appropriately communicated through scientific exchange with Key… more
- CSL Behring (King Of Prussia, PA)
- …qualifications in scientific or business related field** + **5+ years' relevant clinical research , or related experience in the pharmaceutical industry** + ... is a hybrid position. You will report to the Director , Clinical Scientist Lead. You will be... clinical trial process** + **Experience overseeing global clinical trials (pharmaceutical or research institute)** +… more
- Penn Medicine (West Chester, PA)
- …clean, and secure for patients, visitors, and staff 2. Assists the Director and Clinical Manager with compliance for policies, procedures, regulations, ... mission of providing the highest level of care to patients, conducting innovative research , and educating future leaders in the field of medicine. Working for this… more
- CSL Behring (King Of Prussia, PA)
- …related disciplines. + Minimum of 5 years of professional work experience in clinical research in the Pharmaceutical Industry, minimum 4 years' experience in ... and implementation of the assigned Global R&D Quality Audit Program with focus on Clinical Development (from early First in Human to late clinical phases) in… more