- Merck & Co. (North Wales, PA)
- …or related field and at least 5 years SAS programming experience in a clinical trial environment orMS in Computer Science, Statistics, Applied Mathematics, Life ... position is a key collaborator with statistics and other project stakeholders in ensuring that project plans...at least 3 years SAS programming experience in a clinical trial environment. Required Skills: Effective interpersonal… more
- Merck & Co. (North Wales, PA)
- …years of experience with all of the following: SAS programming in a clinical trial environment including data steps, procedures, SAS/MACRO, and SAS/GRAPH; ... of potential medical breakthroughs.Review the quality and reliability of clinical studies using deep scientific knowledge, statistical analysis and high-quality… more
- CSL Behring (King Of Prussia, PA)
- **The Opportunity** The Clinical Trial Supply (CTS) Senior Study Manager manages the end-to-end supply chain for assigned clinical studies throughout the ... multi-year study lifecycle. The CTS Senior Study Manager independently leads clinical studies...to clinical sites and patients. + Develop clinical trial supply documents and training to… more
- Merck (West Point, PA)
- …as the GCS spokesperson at clinical development related meetings (ie, Clinical Trial Teams) and product development related meetings. The incumbent must ... but are not limited to:** + Participates as a key stakeholder on the Clinical Trial Teams (CTT) and collaborates closely with other functional area… more
- Merck (West Point, PA)
- …activities include, but are not limited to:** + Participates on the Clinical Trial Team(CTT)and collaborates closely with other functional area representatives ... Trade, Distribution, Operations etc.) as well asother organizations such as Global Clinical Trial Operations (GCTO) Regional colleagues and Global Development… more
- Merck (Upper Gwynedd, PA)
- …include, but are not limited to: + Collaborate closely with biomarker scientists and project teams to plan clinical trial biomarker set-up using logistical ... **Preferred Experience and Skills:** + Drug discovery experience, including familiarity with clinical trial execution in Oncology studies + Biomarker assay… more
- Pfizer (Collegeville, PA)
- …of drug development process and data operations required for the reporting of clinical trial data (eg data review, study reports, regulatory submissions, safety ... in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities… more
- Pfizer (Collegeville, PA)
- …of consistent, efficient, and quality processes to meet timelines and deliverables. + Serve as Clinical Data Scientist and Trial Lead for one or more clinical ... discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and... Practices (GCDMP), and related regulatory requirements + Strong Project and Risk Management + Strong verbal and written… more
- Organon & Co. (Plymouth Meeting, PA)
- …Officer, and is accountable for: + The leadership of the following teams: Global Clinical Development (GCD), Clinical Trial Operations (CTO), Clinical ... issues and risks. + As member of the Organon Senior Leaders team contributing by driving our Company into...other areas. + Leadership of the following teams: Global Clinical Development, Clinical Trial Operations,… more
- J&J Family of Companies (Titusville, NJ)
- …discovery and the clinical development plans, works on the development of the clinical trial protocol, clinical trial materials, oversees and ... Responsible for the development and execution of the ED clinical trial protocol(s); ensures quality implementation of...and written results of product research, in concert with senior clinical personnel, in preparation for health… more
- Pfizer (Collegeville, PA)
- …Therapeutic Areas. Your project management skills will be leveraged to develop clinical trial timelines and oversee budgets for the assigned clinical ... Medicine, Anti-Infectives, or Inflammation & Immunology preferred. + Broad experience in a Clinical Trial Execution discipline (eg senior study management… more
- Merck (Upper Gwynedd, PA)
- …+ Lead research activities for innovative statistical methods and applications in clinical trial development. + Collaborates in publication of research results ... oral and written reports to effectively communicate results of clinical trials to the project team, our...R. + Solid understanding of worldwide regulatory requirements and clinical trial expertise from phase II to… more
- Merck (North Wales, PA)
- …or related field and at least 5 years SAS programming experience in a clinical trial environment or + MS in Computer Science, Statistics, Applied Mathematics, ... position is a key collaborator with statistics and other project stakeholders in ensuring that project plans...at least 3 years SAS programming experience in a clinical trial environment. **Required Skills:** + Effective… more
- System One (King Of Prussia, PA)
- …PA Onsite Full time permanent - Direct with the client If you are a Senior Clinical Data Manager with experience working at a pharmaceutical company, overseeing ... the lead study data manager for a large, complex trial or multiple, smaller studies. Will support CDM process...Team, work collaboratively with cross-functional team members to meet project deliverables with quality and per agreed timelines *… more
- Merck (North Wales, PA)
- …optimal trial design and monitoring of studies, producing high-quality clinical documents and presentations. The position requires a solid understanding of the ... excellence in the late development of assets within the Metabolism Section of Global Clinical Development + May serve as a senior therapeutic area content expert… more
- University of Pennsylvania (Philadelphia, PA)
- …will develop study protocols, manage contracts and IRB regulatory issues, and oversee clinical trial data management. CRC-C will assist team of research ... Clinical Research Coordinator-C who will take on a senior research role within the Traumatic Brain Injury ...brain injury. CRC-C will take an active role in project oversight, supported by clinical research assistants… more
- Merck (North Wales, PA)
- …years of experience with all of the following: SAS programming in a clinical trial environment including data steps, procedures, SAS/MACRO, and SAS/GRAPH; ... potential medical breakthroughs. + Review the quality and reliability of clinical studies using deep scientific knowledge, statistical analysis and high-quality data… more
- Pfizer (Collegeville, PA)
- …inspection experience + Process and system management experience + Detailed knowledge of clinical trial processes and relationships required + Knowledge of GCP ... The " Senior Issue Lead, Inspections" will be accountable to...inspection responsibilities around: + Directing asset/study team colleagues within CS&O/ Clinical to ensure successful inspection and audit outcomes +… more
- J&J Family of Companies (Spring House, PA)
- …LLC (6084) **Relocation Eligible:** No **Travel** Yes, 25 % of the Time **Job Function** Clinical Trial Project Management **Req ID:** 2406201295W ... impact to participant health and wellbeing by reinventing the clinical trial experience. The Innovative Health Engagement...& Advocacy and as an active member of the senior leadership team, the leader will be instrumental in… more
- Lilly (Philadelphia, PA)
- …Operations) in the planning and execution of a manufacturing strategy to meet clinical trial supply requirements. + Manage the creation of, and lifecycle, ... organizations (CMO) globally to ensure reliable and sufficient supply to Avid/Lilly clinical trials. + Develop, implement, and execute upon supply chain strategy for… more
