- 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)
- …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...analyses , and/or develops mitigation strategies for review with clinical partners and senior leaders.- - Works… 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 ... effectively communicate with stakeholders at various levels, including cross-functional teams, senior management, external vendors, and clinical sites. Strong… more
- 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 ... Skills:Adaptability, Adaptability, Clinical Data, Clinical Operations, Clinical Research, Clinical Study Design, Clinical Testing, Clinical… more
- Taiho Oncology (FL)
- …health care practitioners on Taiho products and relevant disease states, and facilitation of clinical research. The Sr . Manager , Medical Field integrates ... Formally known as Medical Science Liaison Position Summary: The Sr . Manager , Medical Field is a field-facing...disease states which are of interest to Taiho Oncology, study methodology, GCP, clinical information, and product… 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 ... Clinical Data, Clinical Data Interpretation, Clinical Operations, Clinical Research, Clinical Study Design, Clinical Testing, Clinical … more
- The University of Chicago (Chicago, IL)
- …all major types of malignancies, blood disorders, and experimental therapies. Job Summary The Senior Clinical Research Data Manager will perform a variety of ... management expert. Responsible for all data management aspects of clinical studies and efficiently performs all data...the compliance, financial and other related aspects of a clinical study . Interprets the data needed for… more
- The University of Miami (Miami, FL)
- …Gordon Center for Research in Medical Education is currently seeking a full time Manager , Clinical Training Operations to work in Miami, FL. The Manager ... leading edge educational programs utilizing advanced technologies and simulation systems. The Manager of Clinical Training Operations helps in the development,… more
- Tulane University Staff (New Orleans, LA)
- …will be independently manage, coordinate, and provide oversight of clinical research study conduct across multiple research studies and trials at multiple ... The Clinical research Project Manager is responsible... clinical trial management including history of overseeing clinical research studies that are completed on… more
- Genmab (NJ)
- …and immunology experience preferredDemonstrated experience authoring protocols, investigator's brochures, and clinical study reports. Senior level candidates ... At Genmab, we are seeking a passionate and experienced Senior Medical Writing Manager to help us...of critical documents such as protocols, investigator's brochures, and clinical study reports.Contribute to Health Authority briefing… 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 ... Environment Implementation of new programs, enhancements & support of Eisai Clinical Computing Environment Support study migration, program validation, technical… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. Summary: The Senior Director, Head of RBQM (Risk Based Quality Monitoring) sets the vision ... Collaboration and partnership with other functions and stakeholders in supporting clinical trial monitoring and execution through RBQM activities. Accountable for… more
- ACROBiosystems Inc. (New York, NY)
- …validation, candidate drug screening and optimization, CMC development, preclinical and clinical studies , commercial production, and companion diagnostics. We ... and encouraging cross-functional collaboration and continuous learning. Job Summary The Senior Sales Specialist will lead commercial activities in the states of… 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 ... Sales Representative also assists their target physicians with their local clinical and educational initiatives by coordinating company resources (eg, counterparts,… 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, ... Statistics, Drug Safety, Medical, Clinical Pharmacology and Biomarker functions with the above by...developing and writing corresponding SAS or other programs. The Senior Programming Manager may also serve as… more
- Merck & Co. (North Wales, PA)
- …with senior cross-functional leadership to optimize efficiencies in the clinical development space. Preferred skills include experience in the application of AI, ... teams both as a direct manager and a second line manager (ie, managers of managers)Demonstrated collaboration with senior cross-functional leadership in… more
- Abbott (Alameda, CA)
- …. This includes but not limited to planning and implementation of clinical studies from concept to clinical study report per timelines and quality ... you will do: Conduct single or multi-center medical device clinical studies . Perform study site...department procedures and applicable regulatory requirements. Responsible for assisting senior staff in planning study conduct, designing… more
- SystImmune, Inc (Princeton, NJ)
- The Contract Manager is responsible for driving site contract and budget negotiations with sites participating in SystImmune clinical trials. This is included ... to Sites' proposed changes to standard contract terms and the study -specific budget parameters (in partnership with other business lines internally), ensuring… more
- Abbott (Santa Clara, CA)
- …directives to staff as well as study sites as directed by your manager . What You'll Work On Writes clinical trial protocols, protocol amendments, clinical ... in more than 160 countries. JOB DESCRIPTION: Job Title Sr . Scientist Clinical Research About Abbott Abbott...study support groups cross-functional teams to assist in clinical strategy, the development of plans, reports and project… more
- Johns Hopkins University (Baltimore, MD)
- We are seeking a Sr . Grants and Contracts Analyst who will provide dedicated professional level sponsored funds management for more than 80% of time with specific ... lead Grants & Contracts position, in departments where a Grants & Contracts Manager doesn't exist. This position works independently on a variety of complex level… more
