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Clinical Trial Jobs in King of Prussia

1 - 11 of 11
1 - 11 of 11
Search Results - Clinical Trial Jobs in King of Prussia
apartmentCSL BehringplaceKing of Prussiaevent_available
projects. Ensure realistic project planning.  •  Oversee the CRO delivery or manage the in-house programming of data sets, outputs, and DDT files of clinical trials and integrated analysis.  •  Plans and leads the design and implementation of complex...
apartmentTechData Service Company LLCplaceKing of Prussialanguagejobvertise.comevent_available
protocols. Develop and validate complex statistical models and SAS programs for analysis, management and reporting of clinical trial and biomarker data; generate and validate safety and efficacy TLFs and analysis datasets (SDTM, ADaM). Req...
apartmentCSL BehringplaceKing of Prussiaevent_available
supporting clinical trial and integrated analyses, annual reporting, regulatory responses, publications, HTA requests and other purposes as needed within one or more therapeutic areas. The individual will work closely with the Senior Director, Clinical...
apartmentCSL BehringplaceKing of Prussiaevent_available
for the clinical trials and regulatory submissions within the program, and is accountable for the statistical deliverables Main Responsibilities: Input to statistical strategy and ensure appropriate statistical methodologies applied to study design and data...
apartmentCSL BehringplaceKing of Prussiaevent_available
and external partners) with cross-functional responsibilities associated with trial execution and overall therapeutic area clinical development planning. Strong communication and presentation skills are required. Main Responsibilities and Accountabilities...
apartmentCSL BehringplaceKing of Prussiaevent_available
knowledge of clinical trial operations and vendor cost structures. Strong attention to detail, organizational skills, and ability to manage multiple priorities. Excellent communication and collaboration skills across functional teams. Preferred: Experience...
apartmentCSL BehringplaceKing of Prussiaevent_available
Coordinate creation and update of SOPs Retain product and process knowledge Skills and Education Required Minimum of 10 years of Clinical Trial and Post-marketing Pharmacovigilance (PV) experience with 5 years of managerial/leadership experience Global...
apartmentCSL BehringplaceKing of Prussiaevent_available
The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions and is accountable...
apartmentCSL BehringplaceKing of Prussiaevent_available
The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions, and is accountable...
apartmentCSL BehringplaceKing of Prussiaevent_available
implements the statistical strategies for the clinical trials and regulatory submissions within the program, and is accountable for the statistical deliverables. Responsibilities:   1.  Input to statistical strategy and ensure appropriate statistical...
apartmentCSL BehringplaceKing of Prussiaevent_available
pediatric study plan considerations, device feasibility assessments, device selection analyses, clinical trial design input, and human factors (formative/summative) study strategy.  •  Ensure accurate and timely change control assessments of change control...

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