- Merck & Co. (Rahway, NJ)
- …team members including clinical directors and study managers to lead/support clinical trial scientific activities in the Atherosclerosis & Metabolism TA.Job ... of clinical protocol(s). Serves as the lead clinical scientist on the clinical trial...clinical data/medical protocol deviations in collaboration with the Clinical Director .Builds talent and capabilities of direct/indirect… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Associate Director , Clinical Scientist This position drives scientific planning, strategy and execution of Phase 1-4 ... execution of clinical protocol(s).Serves as the lead clinical scientist on the clinical trial... clinical data/medical protocol-deviations in collaboration with the Clinical Director .Builds talent and capabilities of direct… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Director , Business Analyst, within Metrics, Analytics & Performance (MAP) will lead activities related to the development, delivery, ... and monitor performance across our portfolio, studies & processes within Global Clinical Trial Operations (GCTO).Primary responsibilities include but are not… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to ... leader (CSL)Study Planning and Execution: Provides input on major milestones of trial , clinical trial plan and contingency planning; Analyzes and updates… 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
- Novo Nordisk Inc. (Plainsboro, NJ)
- …the head of Clinical , medical, Regulatory (CMR) Business Operations, the Associate Director (AD) is responsible for structuring facilitating and monitoring ... and other key internal stakeholders. In the execution of specific projects, the Associate Director , will be accountable for managing relationships with internal… more
- Genmab (Plainsboro, NJ)
- …as trial responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and ... to be our best, and authentic is essential to fulfilling our purpose.The RoleThe Associate Director acts as a statistical expert supporting the clinical … more
- Genmab (Plainsboro, NJ)
- …ongoing surveillance (including signal detection/evaluation) of safety data from Genmab clinical trials. Be the primary safety contact for other departments and ... review and input to various documents including but not limited to: Trial Protocols, eCRFs/CRFs, and TMFs. Contribute to the development of other documentation… more
- Genmab (Plainsboro, NJ)
- …best, and authentic is essential to fulfilling our purpose.The Role & DepartmentThe Associate Director , Vendor Management, will play a pivotal role in managing ... efficient and effective trial operations.Point of Contact for Global Clinical Trial Managers: Act as the primary point of contact, facilitate communication… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating a distinct R&D ... across multiple functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio Lead. Essential Functions Serve as a member… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …decisions (phase I trials) Provide safety input to Product Development Plan (PDP), Trial Outline, Protocol, Clinical Trial Report, Investigator's Brochure ... external stakeholders. Relationships This position will report to Senior Director Safety Surveillance, US East Coast Development Hub. Key...Responsible for all areas related to patient safety in clinical trials Act as member of the trial… more
- Genmab (Plainsboro, NJ)
- …and/or leading a small team to complete various programming efforts within a clinical trial .You will be responsible for ensuring integrity, consistency, and ... Director , Programming, and work closely with Data Management, Clinical Programming, Statistics, Medical Writing, and other functions as necessary.Position level… more
- Lilly (Branchburg, NJ)
- …life better for people around the world. **Position Description:** The Clinical Trial (CT) Supply Management Associate Director will provide operational ... to improve performance and speed drug development. **Responsibilities:** + Deliver improved clinical trial supply chain performance, assess and mitigate risk,… more
- Actalent (New York, NY)
- …This role is primarily a tactical study delivery role, reporting into an Associate Director or above responsible for Operational Study Strategy. Responsibilities ... Job Title: Clinical Study ManagerJob Description The incumbent will be...audit activities. + Provide oversight of the transmittal of trial and site-level documents to the Document Control Center… more
- Merck (Rahway, NJ)
- **Job Description** **Position Description:** ** Associate Director , Clinical Scientist** This position drives scientific planning, strategy and execution of ... team members including clinical directors and study managers to lead/support clinical trial scientific activities. Job Responsibilities + Responsible for the… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- … Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, evaluation, ... scientific integrity and interpretation of study data of a clinical development program. The Associate Director...clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments + Authors… more
- Regeneron Pharmaceuticals (Armonk, NY)
- The Associate Director , Precision Medicine Clinical Laboratory Operations will be responsible for Clinical Laboratory Project & Program management for ... be done in collaboration with Precision Medicine Strategy Leads, Clinical Trial Management, Clinical Laboratory...early and late-stage programs within our pipeline. **As an Associate Director , a typical day may include… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- The Associate Director , Clinical Sciences contributes to the development, evaluation, planning and execution of hematology clinical studies and ensures ... on clinical studies and programs. As an Associate Director , a typical day may include...clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments. Authors and/or… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to ... + Study Planning and Execution: Provides input on major milestones of trial , clinical trial plan and contingency planning; Analyzes and updates management… more
- Bristol Myers Squibb (Madison, NJ)
- …. **Position Summary** Global Data Management (GDM) is responsible for clinical trial data acquisition, data standards governance, data management, ... trials across the BMS Research & Development portfolio. The Associate Director , External Data Acquisition is a...Acquisition is a leadership role with oversight of external clinical trial data acquisition and integration and… more
