- Merck & Co. (North Wales, PA)
- …and statistical analysis methods fundamental to effective pharmaceutical R&D.- The Clinical Safety Statistics (CSS) group within BARDS supports proactive assessment, ... Lead and provide statistical support for related drug/vaccine projects in Clinical Safety StatisticsInteract with Safety Physicians, Safety Scientists, Clinical … more
- Merck & Co. (North Wales, PA)
- …This position supports statistical programming activities for late stage drug/vaccine clinical development projects. This may include leadership of one or more ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… more
- Merck & Co. (North Wales, PA)
- …programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… more
- Merck & Co. (North Wales, PA)
- …in collaboration with Data Management/Programming. Collaborate cross-functionally to monitor clinical data to ensure quality , completeness, and integrity ... Job DescriptionResponsibilities: Serve as the lead clinical scientist on the clinical trial...are proud to be a company that embraces the value of bringing diverse, talented, and committed people together.… more
- Merck & Co. (North Wales, PA)
- …projects under supervision in Late Development Statistics. --Interacts with Clinical , Regulatory, Statistical Programming, Data Management and other of our ... company's Research Laboratories Scientists in designing and analyzing clinical trials, and in coordinating the statistical activities for clinical drug/vaccine… more
- Merck & Co. (North Wales, PA)
- …GCTO organization prepares a variety of regulated documentation in support of the clinical development portfolio and compliance in public disclosure of clinical ... development and management of informed consent deliverables that support the clinical regulatory writing portfolio while ensuring compliance with internal policy and… more
- Merck & Co. (North Wales, PA)
- …analyze the safety and efficacy claims of potential medical breakthroughs.Review the quality and reliability of clinical studies using deep scientific knowledge, ... statistical analysis and high- quality data to support decision making in ...are proud to be a company that embraces the value of bringing diverse, talented, and committed people together.… more
- Merck & Co. (North Wales, PA)
- …to engage key stakeholders.Demonstrated success in the assurance of deliverable quality and process compliance.Familiarity with statistics and clinical data ... 9 years Statistical Analysis System (SAS) programming experience in a clinical trial environment.MS (preferred) in Computer Science, Statistics, Applied Mathematics,… more
- Merck & Co. (North Wales, PA)
- …Manufacturing and Control (CMC) as well as other functional areas (eg, Clinical Research, Safety Assessment).Supports maintenance (eg, quality compliance and ... needed.Division/AreaResearch and Development Division - Global Regulatory Affairs and Clinical SafetyJob Level/ Grade- 400Reports toGlobal Regulatory Liaison, Executive… more
- Merck & Co. (North Wales, PA)
- …research studies specifically related to Patient-Reported Outcomes (PROs) and Clinical Outcome Assessments (COA). This is an exciting opportunity to ... internal review process for approval, and upload to department repositoryParticipate in quality control assessments and ensure integrity of study data for reports… more
- Merck & Co. (Lower Gwynedd, PA)
- …bioanalytical vaccine immunogenicity assays to support regulated preclinical and clinical vaccine development. The individual will be responsible to contribute ... for the execution of method development, qualification/validation, troubleshooting and/or pre- clinical / clinical sample analysis as needed. Operation, understanding,… more
- Penn State Health (Hershey, PA)
- …Job Applicants PDF for more detailed steps for assistance._ **Union:** Non Bargained **Position** ( HYBRID ) Clinical Quality Value Analysis Specialist - ... is supportive of GPO contracts and processes. + Facilitates and coordinates agenda for Clinical Quality Value Analysis teams. + Supports backorder management… more
- Merck (West Point, PA)
- …with key partner organizations(as a lead GCS Planning program representative) such as clinical development, regulatory, quality and other supply chain areas to ... **Job Description** The Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full… more
- Merck (West Point, PA)
- …Global Clinical Trial Operations (GCTO) Regional colleagues and Global Development Quality (GDQ) to address clinical supply related topics. + Responsible and ... **Job Description** The Global Clinical Supply (GCS) organization is accountable for managing...are proud to be a company that embraces the value of bringing diverse, talented, and committed people together.… more
- Merck (West Point, PA)
- …for clinical supplies. + Interacts with key partner organizations such as clinical development, regulatory, quality and other supply chain areas to address ... **Job Description** The Global Clinical Supply (GCS) organization is accountable for managing...are proud to be a company that embraces the value of bringing diverse, talented, and committed people together.… more
- Merck (North Wales, PA)
- …and statistical analysis methods fundamental to effective pharmaceutical R&D. The Clinical Safety Statistics (CSS) group within BARDS supports proactive assessment, ... Teams. Lead and provide statistical support for related drug/vaccine projects in Clinical Safety Statistics + Interact with Safety Physicians, Safety Scientists, … more
- Merck (West Point, PA)
- **Job Description** Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical ... Response System User Acceptance Testing. + Responsible for the quality review of the URS and UAT deliverables +...Experience:** + 3 years of relevant experience. + Prior clinical trials experience preferred. + Prior (but not required)… more
- Merck (North Wales, PA)
- …This position supports statistical programming activities for late stage drug/vaccine clinical development projects. This may include leadership of one or more ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.… more
- Merck (North Wales, PA)
- …programming activities for multiple and/or late stage drug/vaccine clinical development projects. Accountability predominantly includes the development and ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.… more
- Merck (West Point, PA)
- **Job Description** Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical ... responsible for providing end-to-end IRT (Interactive Response Technology) & COA ( Clinical Outcome Assessment) systems project management support including, but not… more
