- Genmab (NJ)
- … preferredDemonstrated experience authoring protocols, investigator's brochures, and clinical study reports. Senior level candidates should also have ... quality, and scientific integrity? At Genmab, we are seeking a passionate and experienced Senior Medical Writing Manager to help us tell the story of our… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …planning and execution of clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in ... a reasonable accommodation. Education:Bachelor's Degree (preferred in Life Sciences) with relevant clinical development experience required2 or more years work … more
- Merck & Co. (Rahway, NJ)
- …Management Section of the GCS Planning organization.- Working independently, the Inventory Manager Clinical Supplies Project Manager (IM CSPM) creates ... and prepares, analyzes, and/or develops mitigation strategies for review with clinical partners and senior leaders.--Responsible and accountable for utilizing… more
- Merck & Co. (Rahway, NJ)
- …the operational/executional arms within the business. Working independently, the Protocol Clinical Supplies Project Manager (Protocol CSPM) designs strategic and ... deliverables and prepares, analyses, and/or develops mitigation strategies for review with clinical partners and senior leaders.--Works directly in the SAP… more
- Merck & Co. (Rahway, NJ)
- … development teams and the operational/executional arms within the business. The Program Clinical Supplies Project Manager (Program CSPM) serves as the primary ... effectively communicate with stakeholders at various levels, including cross-functional teams, senior management, external vendors, and clinical sites. Strong… more
- Genmab (NJ)
- …the pharmaceutical industry for Programming Manager , at least 6-8 years of experience for Senior Programming ManagerHas experience working in a global ... the above by developing and writing corresponding SAS or other programs. The Senior Programming Manager may also serve as a compound lead.Responsibilities/tasks… more
- Eisai, Inc (NJ)
- …using MS OfficeEisai Salary Transparency Language:The base salary range for the Senior Manager , eTMF System is from :114,600-150,500Under current guidelines, ... profile, we want to hear from you. The Sr. Manager is to lead collaboration efforts with RandD IT...the daily global eTMF system related activities relating to clinical study Trial Master Files (TMF), ensuring regulatory inspection-readiness… more
- Aequor (Thousand Oaks, CA)
- …- preferably PST Ideal Candidate: 5 YOE of biotech / pharma specific experience . MS project knowledge, Smartsheet, Planisware. Nice to have: CMC experience . ... current job responsibilities. is searching for a Sr. Project Manager in our CMC Integration team within Operation Products...stakeholders, the Sr PM will need to understand the Clinical Development Plan and strategy to enable alignment with… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …human-centered experiences, where innovation meets customer-centricity, driving the ultimate experience for our patients. Our focus extends beyond transactions to ... new initiatives related to NovoCare® digital services Oversee NovoCare.com user experience and ensure content is accurate, relevant and aligned with organizational… more
- Eisai, Inc (Nutley, NJ)
- …Data Review programming and JReview within IODS. Reporting to the Assoc. Director of Clinical Programming is the senior level highly technical SAS and JReview ... 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
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