- Merck & Co. (Rahway, NJ)
- …supply chain across the full c ompany's Research & Development Division portfolio of clinical trial s .- GCS is accountable for the planning, sourcing, labeling, ... within the business.-- - - Working independently, the Protocol Clinical Supplies Project Manager ( Protocol CSPM)...at clinical development related meetings (i .e., Clinical Trial Team s ) and product… more
- Merck & Co. (Rahway, NJ)
- …Management Section of the GCS Planning organization. -Working independently, the Inventory Manager Clinical Supplies Project Manager (IM CSPM) creates ... of product.Primary activities include, but are not limited to:-Participates on the Clinical Trial Team (CTT) and collaborates closely with other functional… more
- Merck & Co. (Rahway, NJ)
- …execution of clinical protocol(s) . This may include: Serving as the lead clinical scientist on the clinical trial team. Leading medical monitoring team ... . , ICF documents/ amendments); Partners with the Study Manager on study deliverables. Ensuring CRF design supports data...skills Strong analytical skills with the ability to interpret clinical trial data and synthesize conclusions Interact… more
- Merck & Co. (North Wales, PA)
- … trials.Job Responsibilities: Responsible for the operational planning, feasibility, and execution of a clinical trial .May serve as the clinical trial ... Clinical Operations, Clinical Research, Clinical Study Design, Clinical Testing, Clinical Trial Compliance, Clinical Trial Management,… more
- Merck & Co. (Rahway, NJ)
- … supply chain across the full Company's Research & Development Division portfolio of clinical trial s .- GCS is accountable for the planning, sourcing, labeling, ... teams and the operational/executional arms within the business.-- - - The Program Clinical Supplies Project Manager (Program CSPM) serves as the primary… more
- Genmab (NJ)
- …Then we would love to have you join us!The Role:The Senior Statistical Manager acts as a biostatistician supporting the clinical development of compounds as ... synopsis, protocols, statistical analysis plans, results meetings presentations and clinical trial reportsCoordinate data transfers from/to business partners… more
- Genmab (NJ)
- …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 ... immunology experience preferredDemonstrated experience authoring protocols, investigator's brochures, and clinical study reports. Senior level candidates should… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Collaboration and partnership with other functions and stakeholders in supporting clinical trial monitoring and execution through RBQM activities. Accountable ... centered around rare diseases and immune disorders. Summary: The Senior Director, Head of RBQM (Risk Based Quality Monitoring)...of direct reports, and mentors or acts as functional manager of skip-level or ex-US staff. This position requires… more
- Novo Nordisk Inc. (San Diego, CA)
- …Sales Representative also assists their target physicians with their local clinical and educational initiatives by coordinating company resources (eg, counterparts, ... the Specialty Field Sales Representative reports to the District Business Manager of the specific sales territory. The Specialty Field Sales Representative… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and leads technical teams in preparation of submission documents to include clinical trial applications/amendments (eg, IND, IMPD, IB) and marketing ... laboratory members, the Contract Manufacturing Organization (CMO), Labeling members and Clinical members. This position works with non-standard problems of some… more
- Genmab (NJ)
- …listings, and figures)(Preferred) Practical knowledge and experience using R to support clinical trial analyses.For US based candidates, the proposed salary band ... 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)
- …decision-making skills, expertise in leading large teams in the development of novel clinical trial designs and analysis methods in oncology, experience in ... including regulatory submissionsDemonstrated history of development and execution of innovative clinical trial designs and exploration of novel analysis methods… more
- Glycomine (Boston, MA)
- …in the quality of life for patients, caregivers, and families. Job Description The Senior Clinical Project Manager / Clinical Project Manager ... phases of clinical trials (Phase I-III). The Senior Clinical Project Manager / Clinical...all start-up documents (example ethics documents for submission), site Clinical Trial Agreements and start up activities… more
- Clinical Dynamix, Inc. (Waltham, MA)
- …Contractor to be in place asap)! Reporting to the Sr . Director, Clinical Excellence Operations the Senior Manager /Associate Director, Records Management ... master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent is responsible...Sciences required, advanced degree preferred. *A minimum 5-6+ years ( Sr . Manager )/8+ years (Associate Director) of relevant… more
- BioSpace (North Chicago, IL)
- …prioritize sophisticated analytics solutions to create value and impact for clinical trial medical monitoring. Drives Analytics innovation and experimentation ... the forefront of decision making via fit-for-purpose solutions. The Sr . Manager , Medical Monitoring Analytics is a...big data, digital sources, real world data, pharmacovigilance data, clinical trial data) Responsible for coaching and… more
- Dana-Farber Cancer Institute (Boston, MA)
- … Research Manager is responsible for tracking and complying with clinical trial performance benchmarks; eg protocol and regulatory compliance, patient ... Overview The Clinical Research Manager (CRM) will work...are responsible for the oversight of their disease group's clinical trial portfolio and all related regulatory,… more
- BioSpace (Salt Lake City, UT)
- …data sets, and sophisticated analytics. We are seeking a highly motivated and skilled Senior Clinical Project Manager within our Clinical Operations ... Clinical Operations. In this role, you will: Lead all aspects of clinical trial execution for one or more programs from IND through proof-of-concept and… more
- University of Washington (Seattle, WA)
- …the Senior Analyst is responsible for drafting and negotiating the terms of clinical trial agreements for clinical trials and research studies across all ... areas. POSITION PURPOSE This position is responsible for drafting intricate and complex clinical trial agreements. These robust agreements cover a variety of… more
- Recursion (New York, NY)
- …biology, high-dimensional and diverse data sets, and sophisticated analytics. We are seeking a Lead, Clinical Data Manager who can lead and oversee end to end ... Filing, archival and inspection readiness of all Data Management Trial Master File (TMF) activities. Review and manage external...and forecasting. The Team You'll Join Reporting to the Senior Director, Clinical Data Management and working… more
- Takeda Pharmaceutical Company Limited (Lexington, MA)
- … Science Lead and TA Medical Teams. Drive and deliver all aspects of clinical trial execution from study concept to final reporting Research and Strategic ... Regulatory, CMC, Marketing). Minimum of 5 years' experience as a clinical project/program manager leading complex pharmaceutical, academic or hospital… more
