- Syneos Health Careers (Morrisville, NC)
- Description Clinical Project Manager II - post- trial access / EAP / rollover studies Syneos Health(R) is a leading fully integrated biopharmaceutical ... Project Leadership and Delivery: *Manages a project as a project manager overseeing interdisciplinary clinical research studies and ensures compliance… more
- Boston Scientific (Marlborough, MA)
- …you'll be supported in progressing - whatever your ambitions. About the role: The Senior Clinical Trial Manager (CTM) will be responsible for the design, ... Coronary Therapies portfolio. The Senior CTM is responsible for leading cross-functional clinical teams in support of the organization's business objectives for… more
- Merck & Co. (Rahway, NJ)
- …arms within the business .-- - - Working independently, the Protocol Clinical Supplies Project Manager ( Protocol CSPM) designs strategic and operational ... full c ompany's Research & Development Division portfolio of clinical trial s .- GCS is accountable...problems, make informed risk decisions considering both technical & business risks, & influence portfolio decisions with facts and… 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)
- …the operational/executional arms within the business .-- - - The Program Clinical Supplies Project Manager (Program CSPM) serves as the primary program-level ... supply chain across the full Company's Research & Development Division portfolio of clinical trial s .- GCS is accountable for the planning, sourcing, labeling,… 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)
- …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 ... organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work... Clinical Research, Clinical Study Design, Clinical Testing, Clinical Trial Compliance,… more
- Genmab (NJ)
- …statistical analysis plans, results meetings presentations and clinical trial reportsCoordinate data transfers from/to business partners in collaboration ... 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
- Medix (Grand Rapids, MI)
- …ensuring efficient workflow and optimal use of team resources, in alignment with Manager defined priorities. Clinical Support Coverage: Maintain clinical ... progress, cycle-time KPIs, staffing utilization; provide weekly status updates to Site Manager and assigned clinical project manager . Staff Performance… 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
- Profound Research (Las Vegas, NV)
- …Never Compromise Quality Role & Responsibilities: -Maintain site compliance for all clinical trial activities in accordance with established research protocols ... Profound Research: Profound Research seeks to drive clinical innovation by partnering with community physicians to offer clinical research as a therapeutic… more
- Genmab (NJ)
- …families and employees.Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly ... are seeking a passionate and experienced Senior Medical Writing Manager to help us tell the story of our...us tell the story of our science through compelling clinical and regulatory documents. You'll be at the heart… more
- Genmab (NJ)
- …statistical analysis plans, results meetings presentations and clinical trial reportsCoordinate data transfers from/to business partners in collaboration ... families and employees.Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly… more
- Merck & Co. (San Francisco, CA)
- …Driving License:Hazardous Material(s):Required Skills:Budget Development, Business , Clinical Supply Chain Management, Clinical Trial ... Director, DSCS Digital Implementation Project ManagerWithin the Development Sciences and Clinical Supply (DSCS) organization, the Digital Project Manager will… more
- Clinical Dynamix, Inc. (Waltham, MA)
- …to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent is responsible for records management activities ... roles within the Pharmaceutical and/Medical Device Industry, with heavy concentration within clinical trial management and monitoring. *A minimum of 5+ years'… 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
- BioSpace (Tarrytown, NY)
- …Director drafts designs of clinical study concepts which lead to clinical trial protocols and is responsible for medical/scientific supervision of individual ... As a Medical Director, a typical day may include the following: Defines clinical trial -related goals and objectives. Conducts literature and database research on… 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 ... employees.Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe...we would love to have you join us!The Programming Manager supports the development of new therapies by ensuring… more
- IQVIA, Inc. (Bountiful, UT)
- …This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the ... conduct of clinical trials. The primary skills include logical thinking, ability..."can-do" attitude, the ability to adapt quickly to changing business conditions, strong interpersonal and team building skills. The… more
