- BioSpace (New York, NY)
- …unable to meet their choline needs via oral or enteral routes. Job Overview: The Clinical Trial Manager (CTM)/ Clinical Research Associate is responsible ... for providing oversight of the Sponsor's outsourced Contracted Research Organizations (CRO) clinical trial services, with a primary focus on ensuring quality … more
- 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 ... product.Primary activities include, but are not limited to:-Participates on the Clinical Trial Team (CTT) and collaborates closely with other functional area… more
- Merck & Co. (North Wales, PA)
- …execution of clinical protocol(s). This may include:Serving as the lead clinical scientist on the clinical trial team.Leading medical monitoring ... and prioritization skills.Strong analytical skills with the ability to interpret clinical trial data and synthesize conclusions.Interact with key stakeholders… 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, ... operational/executional arms within the business.-- - - The Program Clinical Supplies Project Manager (Program CSPM) serves...- - The Program Clinical Supplies Project Manager (Program CSPM) serves as the primary program-level GCS… 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. (North Wales, PA)
- …trials.Job ResponsibilitiesResponsible for the operational planning, feasibility, execution and conduct of clinical trial (s).Serves as the Clinical Trial ... (study team, subsidiary country teams, vendors, committees, etc.) in support of clinical trial objectives.Liaises with partners, vendors, and vendor management… more
- Genmab (NJ)
- …synopsis, protocols, statistical analysis plans, results meetings presentations and clinical trial reportsCoordinate data transfers from/to business partners ... join us!Role:The Associate Director acts as a statistical expert supporting the clinical development of compounds as compound and/or indication lead for both early… more
- Genmab (NJ)
- …synopsis, protocols, statistical analysis plans, results meetings presentations and clinical trial reportsCoordinate data transfers from/to business partners ... fit? 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… more
- Merck & Co. (San Francisco, CA)
- …Arrangements:HybridShift:Valid Driving License:Hazardous Material(s):Required Skills:Budget Development, Business, Clinical Supply Chain Management, Clinical ... Director, DSCS Digital Implementation Project ManagerWithin the Development Sciences and Clinical Supply (DSCS) organization, the Digital Project Manager will… more
- Genmab (NJ)
- …integrity? At Genmab, we are seeking a passionate and experienced Senior Medical Writing Manager to help us tell the story of our science through compelling ... clinical and regulatory documents. You'll be at the heart...regulatory submissions (eg, NDA, BLA, MAA).Drive collaboration with cross-functional trial teams to manage timelines, facilitate meetings, and lead… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. SummaryThe Manager Audits & Compliance, GCP/Document Audits supports end-to-end audit activities ... audits assigned. Support conduct of document audits including eTMF, Clinical Study Reports and Common Technical Document submission.ResponsibilitiesSupport audit… more
- Novo Nordisk Inc. (Hackensack, NJ)
- …The EDCS must achieve sales goals by utilizing a patient-centric and clinical approach to engaging their customers and promoting Novo Nordisks portfolio of ... assess, create and maintain advocacy of customers aligned to company, brand and clinical goals; the EDCS develops local strategies and executes local tactical plans… more
- Novo Nordisk Inc. (Seattle, WA)
- …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
- 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 ... we would love to have you join us!The Programming Manager supports the development of new therapies by ensuring...will support the Data Management, Statistics, Drug Safety, Medical, Clinical Pharmacology and Biomarker functions with the above by… 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 ... regulatory submissionsDemonstrated history of development and execution of innovative clinical trial designs and exploration of novel...and maintaining high performing teams both as a direct manager and a second line manager (ie,… more
- Formation Bio (New York, NY)
- …in program execution, ensuring the team stays at the forefront of innovation in clinical trial operations. About You You're excited about the intersection of AI ... progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately...at Formation Bio. This role requires an experienced program manager who can oversee at least one drug development… 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 ... technical and career, of direct reports, and mentors or acts as functional manager of skip-level or ex-US staff. This position requires strong knowledge about RBQM,… 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
