- Merck & Co. (Rahway, NJ)
- …and SAP team members to further extend capabilities and functionalities on our existing Clinical Trial Supply Management (CTSM) solution in order to satisfy and ... Management and Distribution areas with a strong focus in Clinical Trial Supply Management (CTSM) is highly...where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please,… more
- Merck & Co. (Rahway, NJ)
- …Develop model-based strategies (translational PK/PD strategies, mechanistic model, POPPK/PD, clinical trial simulations, etc) for quantitative analyses, within ... phases of drug development including, but not limited to dose selection, clinical trial design, and go/no-go decisionsCollaborate with other functional areas,… more
- Merck & Co. (North Wales, PA)
- …and retention efforts to achieve study milestonesUpon request from Global Clinical Trial Operations (GCTO),Recommends study sites and identifies potential ... to 50% travel required with some overnight.Role Summary The Regional Medical Scientific Director - GI Oncology is a credentialed (ie, PhD, PharmD, DNP, MD)… more
- Merck & Co. (Rahway, NJ)
- …translational PK/PD approaches, population pharmacokinetic models, exposure-response models, clinical trial simulation, disease progression models, quantitative ... and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial applications… more
- Merck & Co. (Rahway, NJ)
- …(popPK), PK/PD models, exposure response (ER) models, model-based meta-analysis (MBMA), clinical trial simulations (CTS) and disease progression modeling into ... company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas.This Associate...seek to improve cycle time, cost/size, number of trials, clinical trial design and Go/No Go decisionsFraming… more
- Merck & Co. (Rahway, NJ)
- …development and qualification of release, characterization, and stability assays for testing of clinical trial material and in support of product and process ... scientific role tasked with working closely with the group Director to define group strategy and to lead a...where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please,… more
- Northeast Georgia Health System, Inc (Gainesville, GA)
- …sponsor / securely stored in a timely manner, eg, 1572, Confidentiality Agreement, clinical trial agreements , IRB approval letter, Financial Disclosures, ... process in line with the approved protocol, including grant sponsored and clinical trial projectsManage and communicate effectively with Research Leadership… more
- SUNY Upstate Medical University (Syracuse, NY)
- …for the Research Foundation for SUNY Point of Contact for review/processing for all Clinical Trial Agreements through the Research Foundation, review of ... CDAs, NDAs and Master Clinical Trial Agreements . Additionally the position will be responsible for assisting all Clinical Research Faculty and staff in… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …and implements innovative solutions to resolve roadblocks in patient recruitment and clinical trial execution via development of an overall outsourcing strategy ... in vendor management, leading CROs/various contracted resources, site monitoring and clinical quality compliance, andmanaging clinical trial budgets… more
- Merck (Rahway, NJ)
- …and therapeutic expertise for the design, planning and execution of early phase clinical trials with the Clinical Director and internal/external team ... design, data or study conduct issues. Reviews and interprets clinical trial data. May conduct on-site study...where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please,… more
- Bristol Myers Squibb (Princeton, NJ)
- …team of outsourcing managers within a specific therapeutic area(s) and manages clinical trial vendor partnerships that supports alliance and outsourcing ... management across multiple service categories of clinical trial activities in R&D. **Key Responsibilities** + Leads a team of Outsourcing Associate Directors and… more
- J&J Family of Companies (Jacksonville, FL)
- … clinical trial including * project timelines, resourcing, budget plans, clinical supply management. * agreements and statements of work (50). * Manage ... Associate Director Clinical Logistics - 2406191308W **Description**...and budgets, when applicable (10%). * Manage and improve clinical trial processes, including benchmarking and leveraging… more
- Teva Pharmaceuticals (West Chester, PA)
- Sr Director Clinical Development Date: Jun 28,... development in respective therapeutic area and involvement in clinical trial design or execution. + A ... to make a difference with. **The opportunity** The Senior Director , Clinical Development is responsible for providing...data + Implementing strategies to identify, monitor and resolve clinical /program trial issues + Serving as the… more
- Merck (Rahway, NJ)
- …and SAP team members to further extend capabilities and functionalities on our existing Clinical Trial Supply Management (CTSM) solution in order to satisfy and ... Management and Distribution areas with a strong focus in Clinical Trial Supply Management (CTSM) is highly...where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please,… more
- Teva Pharmaceuticals (West Chester, PA)
- Director Clinical Development - Oncology Date: Jun 27, 2024 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals Job Id: ... clinical programs worldwide across all phases of clinical research. The Director will oversee study...cross-functional clinical development team + Supports Global Clinical Operations in clinical trial … more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …regulatory agency meetings, and oversees departmental activities with regards to clinical trial conduct and regulatory submissions. **Responsibilities** + ... related requirements. + Experience preparing and overseeing regulatory submissions, including INDs/ Clinical Trial Applications and Marketing Applications in eCTD… more
- University of Pennsylvania (Philadelphia, PA)
- …Best Practices and Work Instruction documents to guide every aspect of the multi-site clinical trial programs. + Train internal and external study teams to ... and resources, and much more. Posted Job Title Program Director Multi-site Clinical Research (Abramson Cancer Center)...NCI. + Create a new system to track financial agreements for each multi-site study and performance milestones to… more
- AbbVie (North Chicago, IL)
- …substantial understanding of relevant therapeutic area is required. Knowledge of clinical trial methodology coupled with performance in registration enabling ... act as a consultant/liaison/resource with other corporations when working under licensing agreements . Responsibilities: Assists in the design of clinical studies… more
- Houston Methodist (Houston, TX)
- …systems, and procedures related to contract review and negotiation and analysis of clinical trial agreements , basic and translational sponsored research ... At Houston Methodist, the Director , Research Contracts position is responsible for providing...operating procedures. + Leverages streamlining strategies such as Master Clinical Trial agreements and standardized… more
- Beth Israel Lahey Health (Boston, MA)
- …Review Board, and other institutional offices to oversee the negotiation of Subcontracts, Clinical Trial Agreements , Data Use Agreements , Billing ... Agreements , and other atypical agreements . The Director 's primary focus will be on developing strategy, enhancing process improvement, improving internal… more
