- Merck & Co. (North Wales, PA)
- …(eg, study team, country teams, vendors, committees) in support of clinical study objectives.Accountable for managing any study specific partners ... Material(s):n/aRequired Skills:Adaptability, Adaptability, Clinical Data, Clinical Operations, Clinical Research, Clinical Study Design, Clinical … more
- Merck & Co. (Rahway, NJ)
- …operational/executional arms within the business.-- - - Working independently, the Protocol Clinical Supplies Project Manager ( Protocol CSPM) designs strategic ... - Responsible and accountable for establishing the timelines for clinical supply needs per study and providing...Clinical Practices (GCP) is highly desirable. - Preferred Experience and Skills: - - - Results-orientation with the… more
- Merck & Co. (Rahway, NJ)
- …Management Section of the GCS Planning organization. -Working independently, the Inventory Manager Clinical Supplies Project Manager (IM CSPM) creates ... strategic and operational plans associated with the downstream activities of clinical supplies for their assigned studies . -The primary function of the IM CSPM… more
- Merck & Co. (Rahway, NJ)
- …teams and the operational/executional arms within the business.-- - - The Program Clinical Supplies Project Manager (Program CSPM) serves as the primary ... ensures proper allocation of drug product as needed across studies within assigned program(s) . - Responsible for identifying...Clinical Practices (GCP) is highly desirable. - Preferred Experience and Skills: - - Proficiency in using supply… more
- Merck & Co. (Rahway, NJ)
- …study materials (e . g . , ICF documents/ amendments); Partners with the Study Manager on study deliverables. Ensuring CRF design supports data collection ... Experience Bachelor's Degree +5 years of pharmaceutical , clinical drug development, project management , and/or medical field... Clinical Data Interpretation, Clinical Operations, Clinical Research, Clinical Study Design,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …GxP audits assigned. Support conduct of document audits including eTMF, Clinical Study Reports and Common Technical Document submission.ResponsibilitiesSupport ... audit program for clinical studies and vendors as applicable for...including, but not limited to Common Technical Document (CTD), Clinical Study Report (CSR) and Nonclinical … more
- Eisai, Inc (Nutley, NJ)
- …Environment Implementation of new programs, enhancements & support of Eisai Clinical Computing Environment Support study migration, program validation, technical ... is your profile, we want to hear from you. The Associate Director, Clinical Programming must have expertise in addressing technical challenges in the programming… more
- BioAgilytix (San Diego, CA)
- … Manager II will lead scientific and operational activities in support of preclinical, clinical , and product release studies for our San Diego lab. This role ... team(s) developing and validating bioanalytical assays for support of preclinical, clinical and product release studies .Motivating team by inspiring employees… more
- Taiho Oncology (FL)
- …care practitioners on Taiho products and relevant disease states, and facilitation of clinical research. The Sr. Manager , Medical Field integrates clinical ... disease states which are of interest to Taiho Oncology, study methodology, GCP, clinical information, and product...a field facing scientific role is preferred and Sr. Manager , Medical Field (MSL) experience is preferred.… more
- Merck & Co. (San Francisco, CA)
- …Director, DSCS Digital Implementation Project ManagerWithin the Development Sciences and Clinical Supply (DSCS) organization, the Digital Project Manager will ... robustness across organizational deliverables.- In this role, the DSCS Digital Project Manager will provide tactical direction and partner with the DSCS Digital… more
- Genmab (NJ)
- … preferredDemonstrated experience authoring protocols, investigator's brochures, and clinical study reports. Senior level candidates should also have ... and editing of critical documents such as protocols, investigator's brochures, and clinical study reports.Contribute to Health Authority briefing documents and… more
- Genmab (NJ)
- …decision making. Responsibilities in leading the programming efforts of at least one study are in scope.The Programming Manager will support the Data Management, ... qualityRequirements:Minimum BSc. or equivalent qualificationsAt least 2-5 years of experience within the pharmaceutical industry for Programming Manager ,… more
- BioAgilytix (San Diego, CA)
- …assess analytical results, troubleshoot issues, and ensure timely completion of studies .Serve as Principal Investigator or Study Director for GLP/validation ... clients and drug modalities, your career can develop rapidly. You'll gain experience with a variety of challenges all while you enable life-changing, life-saving… more
- ACROBiosystems Inc. (San Diego, CA)
- …validation, candidate drug screening and optimization, CMC development, preclinical and clinical studies , commercial production, and companion diagnostics. We ... collaboration and continuous learning. Job Summary The Regional Marketing Manager will develop, execute, and monitor local marketing strategies across… more
- ACROBiosystems Inc. (Boston, MA)
- …validation, candidate drug screening and optimization, CMC development, preclinical and clinical studies , commercial production, and companion diagnostics. We ... cross-functional collaboration and continuous learning. Job Summary The Regional Sales Manager will oversee commercial activities in the Greater Boston area,… more
- Novo Nordisk Inc. (Olive Branch, MS)
- …and modify customer engagement and sales strategies Understand the most up-to-date clinical studies to educate customers and improve ability to anticipate ... maintain advocacy of customers aligned to company, brand and clinical goals. The OCS develops local strategies and executes...health. Internally, the OCS reports to the District Business Manager of the specific sales territory. The OCS also… more
- Merck & Co. (North Wales, PA)
- …of novel clinical trial designs and analysis methods in oncology, experience in directing multiple teams to execute on business priorities, demonstrated ... collaboration with senior cross-functional leadership to optimize efficiencies in the clinical development space. Preferred skills include experience in the… more
- Novo Nordisk Inc. (San Diego, CA)
- …improved patient health Demonstrates thorough knowledge of all promoted NNI approved clinical studies and the skill to engage customers (prescribers, support ... navigate PA's in rapidly developing market Health Systems and/or Institutional Account experience is preferred Clinical approach to selling and engaging… more
- BioAgilytix (Durham, NC)
- …chromatographic and mass spectrometric (LC/MS) techniques in support of preclinical, clinical , and product release studies .Design, plan, and execute experiments ... clients and drug modalities, your career can develop rapidly. You'll gain experience with a variety of challenges all while you enable life-changing, life-saving… more
- Novo Nordisk Inc. (Charlotte, NC)
- …products and services for their patients Maintain knowledge of the most recent clinical studies to inform customers and address questions, concerns, and ... Health System Portfolio Specialist I reports to the Ecosystem District Business Manager . The Health System Portfolio Specialist I also must work collaboratively work… more
