- 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
- University of Pennsylvania (Philadelphia, PA)
- …technology/systems required to enhance clinical research operations. In this role, the Sr Clinical Trial Project Manager will independently manage ... of health and wellness programs and resources, and much more. Posted Job Title Sr . Clinical Trial Project Manager (Center for Cellular Immunotherapy) Job… 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 ... Sr . Director, Engagement - 2406201295W **Description** **Johnson &...impact to participant health and wellbeing by reinventing the clinical trial experience. The Innovative Health Engagement… 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
- 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
- Insight Global (Malvern, PA)
- …-Outstanding EM issues -Transfer of document to the EM -Status of Clinical Trial Material (CTM) lots/production schedule -Various workstreams (help build ... our large pharmaceutical clients is looking to hire a Sr Quality Specialist to join the EQ team. The...team, and help to ensure that all quality-related activities project goals and deadlines are met. In particular, the… more
- IQVIA (Wayne, PA)
- …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines *… 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
- 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
- University of Pennsylvania (Philadelphia, PA)
- …protocol. Show vigilance in patient safety, protocol compliance and data quality. Communicate clinical trial patient activity to the Infusion Pharmacist at PAH ... programs and resources, and much more. Posted Job Title Clinical Research Project Manager A/B (Abramson Cancer...budget preparation for trials as needed. May support a clinical trial budget through each phase of… 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
- System One (King Of Prussia, PA)
- Title: Sr CDM II Location: King of Prussia, PA Onsite...- Direct with the client If you are a Senior Clinical Data Manager with experience working at ... 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 (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
- 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
