- Bausch + Lomb (Harrisburg, PA)
- …updates on progress and changes in scope, schedule, and resources. + Organize investigator and expert meetings relevant to the indication and assist with the ... forms (queries) are appropriately handled by the CRAs and responded to by the site/ investigator in a timely manner. May assist in the review of queries to determine… more
- University of Pennsylvania (Philadelphia, PA)
- …Clinical Research Coordinator A: This position will support the management of 3 -4 clinical research studies (all phases) that involve assessment of investigational ... and COPD. Under the indirect supervision (minimal supervision) of the Principal Investigator (PI) and direct supervision of the Clinical Research Coordinator C… more
- Sumitomo Pharma (Pittsburgh, PA)
- …drug/brand development. + Identify, initiate, coordinate, evaluate and monitor investigator -sponsored studies intended to support the clinical and scientific ... products. + Help develop and manage timelines of publication plans of investigator -sponsored studies. + Assist in the identification, evaluation, and engagement of… more
- University of Pennsylvania (Philadelphia, PA)
- …research protocols, as well as assist in the conduct of investigator -initiated research and division-specific research projects and operations. This position's ... in study team meetings, disease site group meetings, and ongoing protocol training/ compliance meetings. Supports in the monitoring of external sites and assists in… more
- University of Pennsylvania (Philadelphia, PA)
- …Coordinator to organize, coordinate and implement different phases of investigator -initiated and industry-sponsored clinical trials of novel therapies or currently ... testing; within the EMR or other tools + Attend Investigator Initiation meetings + Obtain slides from pathology and...and/or CROs. + Show vigilance in patient safety, protocol compliance , and data quality. + Adhere to all University… more
- Merck (North Wales, PA)
- …for approved, in-development, and active Company-sponsored trials and/or investigator -sponsored research studies. The Regional Medical Scientific Director serves ... the comprehension of the scientific foundations and goals of investigator -sponsored research + Identifies barriers to patient enrollment and...or MD + Proven competence and a minimum of 3 years of relevant therapeutic area experience beyond that… more
- Merck (Harrisburg, PA)
- …for approved, in-development, and active Company-sponsored trials and/or investigator -sponsored research studies. The Regional Medical Scientific Director serves ... the comprehension of the scientific foundations and goals of investigator -sponsored research + Identifies barriers to patient enrollment and...or MD + Proven competence and a minimum of 3 years of relevant therapeutic area experience beyond that… more
- Greene Tweed (Kulpsville, PA)
- …regulations and corporate HSE initiatives. + Conducts activities to support compliance obligations associated with applicable federal, state, and local HSE ... coordinating action plans to close out findings as necessary to ensure compliance and effective performance. + Participates in and/or conducts routine HSE… more
- University of Pennsylvania (Philadelphia, PA)
- …inspections. The CRC will participate in study team meetings and ongoing protocol training/ compliance meetings and will be expected to adhere to all University of ... processing/handling. The CRC will demonstrate vigilance in patient safety, protocol compliance , and data quality, and will participate in data organization for… more
- University of Pennsylvania (Philadelphia, PA)
- …in the Takeshita Lab is to independently coordinate the regulatory compliance and operations of research protocols including quantitative, qualitative, and mixed ... to the study PI and collaborating investigators. They will also engage in compliance monitoring and data management with other study team members including the data… more
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