- Taiho Oncology (Princeton, NJ)
- …to transforming the landscape of cancer treatment and improving patients' lives. As a Senior Manager , Clinical Research Scientist, you will play a pivotal ... at the forefront of cancer research. Position Summary: The Senior Manager , Clinical Research Scientist...conferences and leverages the knowledge for designing and summarizing clinical studies . + Keeps Sr .… more
- University of Pennsylvania (Philadelphia, PA)
- …of health and wellness programs and resources, and much more. Posted Job Title Manager , Clinical Research Finance Operations (Office of Clinical Research) ... D, Research, Administration Job Description Summary Responsible for the overall clinical research financial management and other financial matters of the… more
- CSL Behring (King Of Prussia, PA)
- …and within the agreed timeframe and budget. + Collaborate with Senior Managers, Clinical Finance to build and maintain robust study costing models for ... to the Associate Director, Business Operations Management, as the ** Manager , Clinical Financial Modeling** , you will...with Clinical Operations and POE to ensure study assumptions for all studies are up-to-date… more
- Bristol Myers Squibb (Princeton, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . **Job Title:** Senior Manager - Analytical AI, Clinical Development **Job ... advance clinical development through data-driven innovation, the Senior Manager - Analytical AI in ...optimize end-to-end pipelines that address critical business problems in clinical study design and execution. + Automate… more
- IQVIA (Philadelphia, PA)
- …Clinical Data Management role. + Your previous roles/job titles may include _Clinical Data Manager , Senior Clinical Data Manager , Lead Data Manager ... now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing us to...You'll Do** + Lead data management for complex, global clinical trials from study setup to database… more
- Taiho Oncology (Princeton, NJ)
- …complex global studies to support the Clinical Development Plan. The Senior Study Manager (SSM) is responsible for ensuring assigned clinical ... and monitor trial milestones as well as overall day-to-day operations of clinical studies , ensuring study information and timelines are accurate in internal… more
- ICON Clinical Research (Blue Bell, PA)
- Clinical Drug Supply Manager ICON plc...IP expiry. Ancillary Supplies + Develop plans for supplying clinical study sites with ancillary supplies, either ... reviews IVRS user manuals; Designs, reviews and approves IP-related study tools (for clinical study ...applies to internally sourced studies and/or CRO/Partnered studies . Collaborates and interacts with clinical trial… more
- Pfizer (Collegeville, PA)
- …groups to ensure study teams are enabled to implement eCOA in clinical studies efficiently, consistently and with the highest quality and lowest regulatory ... the Clinical Development &Operations (CD&O) organization, the Senior Associate, eCOA Manager , Clinical ...of the Patient Data Strategies (PDS) team in helping clinical study teams use assigned patient data… more
- Bristol Myers Squibb (Princeton, NJ)
- …and execution of multiple clinical trials (eg significant experience as a senior clinical leader), and exhibits all of the following attributes: + Able ... and achieve results through teams, and is the direct manager to Clinical Trial Physicians (CTPs) **Key...studies , with the support of the CTPs and Clinical Scientists (CS) within the asset and/or indication +… more
- University of Pennsylvania (Philadelphia, PA)
- …Efficient time management and the ability to multitask to complete activities for multiple clinical studies at a given time are essential. This position requires ... Development & Efficacy (PDE) Manager Job Profile Title Technical Operations Manager - Clinical Cell and Vaccine Production Facility Job Description Summary… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- **Job Summary** The Senior Manager of Global Quality Management (GQM) supports the execution of clinical quality activities to ensure compliance with Good ... throughout the clinical development lifecycle. **Key Responsibilities** ** Clinical Study Support** + Serve as a...+ Monitor audit trends and escalate recurring issues to senior leadership. **Quality Systems & Compliance** + Support the… more
- IQVIA (Philadelphia, PA)
- …is a member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and ... with the core project team and/or sub-team. + Accountable for assigned portion of clinical studies as per the contract while optimizing speed, quality and cost… more
- IQVIA (Abington, PA)
- … Clinical Lead is a member of the core project team responsible for clinical delivery of clinical studies to meet contractual requirements in accordance ... on projects with 1-2 service lines and single/few countries or alongside more senior Clinical Leads to deliver large, global trials.; * May attend site visits as… more
- Pfizer (Collegeville, PA)
- …informed consent documents, and contributes to authoring of IBs, site training materials, clinical study reports, regulatory responses, and other clinical ... for programs within the Late-Stage Oncology portfolio. **KEY RESPONSIBILITIES** + Clinical development expert for assigned studies maintaining current scientific… more
- Kelly Services (West Point, PA)
- ** Senior Study Manager I**...Immunology** **Description of Services** May lead or support a study or studies , depending on size/complexity. As ... change orders for vendors, as necessary + Responsible for end of study reconciliation ( clinical & ancillary supplies) + Oversees all HQ close-out tasks +… more
- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Clinical Trial Physician sits within Clinical Development, which ... studies + Leads the analysis of benefit/risk for clinical development protocols in a matrix team environment working...key Health Authority interactions and advisory board meetings as Senior Clinical Trial Physician + Authors/drafts … more
- Parexel (Trenton, NJ)
- …for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies , in compliance with Client Procedural Documents, international ... **CRA and Sr CRA positions- Remote - Need for SE...escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance… more
- Taiho Oncology (Princeton, NJ)
- … documents related to clinical studies as outlined by the manager . + Attend study site initiation visits (SIV) and provides therapeutic area, compound, ... (IB), informed consent forms (ICF), case report forms (CRF), Clinical study report (CSR), NDA/MAA registration documents,...Institutional Review Boards/ Ethics Committees (IRBs/ECs) relevant to the studies . + Review and sign off on clinical… more
- Taiho Oncology (Princeton, NJ)
- …standards and guidance documents + Serve as regulatory lead for assigned activities and clinical study teams. + Provide updates to project/ study teams on ... Hybrid Employee Value Proposition: Join our dynamic and expanding mid-size company as a Sr . Manager , Regulatory Affairs Strategy. In this role, you will support… more
- J&J Family of Companies (Horsham, PA)
- …therapeutic areas and providing research support for company as well as investigator-initiated studies . The Senior Medical Science Liaison will: + Develop and ... apply. We are searching for the best talent for Sr . Medical Science Liaison, Lung Oncology, to be based...(Maine, Massachusetts, New Hampshire, Rhode Island and Vermont). The Senior Medical Science Liaison (MSL) is considered the field-… more