- Merck & Co. (Rahway, NJ)
- …organizations ( as a lead GCS Planning program representative ) such as clinical development, regulatory, quality and other supply chain areas to negotiate ... Business, Business Risks, Change Management, Clinical Development, Clinical Research, Cross-Functional Team Leadership, Data Analysis, Detail-Oriented,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …appropriate biomarker, PK / PD measurements; Reviews emerging clinical data regularly; Leads dose-escalation meetings; Performs quality assessment with ... size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member...& Data Ops for EDC, edit checks, data quality listings, SAP, Data … more
- Merck & Co. (North Wales, PA)
- …be programmed, an understanding of statistical terminology and concepts.Familiarity with clinical data management conceptsExperience in CDISC and ADaM ... Specific Required Skills and Experience: Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH;… more
- Merck & Co. (San Francisco, CA)
- Job Description Position Description: Associate Director, DSCS Digital Implementation Project ManagerWithin the Development Sciences and Clinical Supply (DSCS) ... execution of our Company's DSCS Digital Strategy to enable a seamless data infrastructure that drives increased speed, capacity and robustness across organizational… more
- Merck & Co. (Rahway, NJ)
- …operations staff, quality representatives, and other team members to ensure the quality of the clinical supplies, the scientific rigor of the processes, and ... License:Hazardous Material(s):Required Skills:Applied Engineering, Applied Engineering, Chemical Engineering, Chemistry, Clinical Operations, Customer-Focused, Data -Driven Decision Making, Drug… more
- Eisai, Inc (Exton, PA)
- … Quality Control, Regulatory, and CMC Program Management departments.The Associate Director of Biologics Operations maintains knowledge of established and ... your profile, we want to hear from you. The Associate Director of Biologics Operations Upstream and Downstream is...in development through their lifecycle (Preclinical through phase III clinical development) at the Biologics Pilot Plant as well… more
- Merck & Co. (Durham, NC)
- …Material(s):n/aRequired Skills:Business, Business Processes, Capital Planning, Clinical Supply Chain Management, Communication, Customer-Focused, ... and Financial audits, input to QSAT actions, to ensure compliance.Support the Master Data team with general Material Handling Steward tasksDrive safety, quality … more
- Insmed Incorporated (Los Angeles, CA)
- …Best Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Associate Director Medical Science Liaison will develop and maintain professional ... and/or product support of appropriate prescribing, improved patient outcomes.Present data on Insmed products to HCPs including physicians, academic institutions,… more
- Aequor (Thousand Oaks, CA)
- …leadership and accountability. Core Competencies: Technical Expertise: o Deep knowledge of clinical data management processes and systems (eg, EDC, CDISC ... Management etc. Determine key performance indicators (KPIs) and suggest data -driven improvements Delivering a quality , fit for...& Knowledge Minimum of 10 years of experience in clinical data management or related field. Proven… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …strategy, focusing on every touchpoint that impacts our customers. We leverage data and insights to inform our decision-making processes, ensuring that our ... design pull you in? Are you ready to experiment with us? The Position The Associate Director of Nephrology Key Opinion Leader Marketing will be a pivotal driver in… more
- Merck & Co. (Rahway, NJ)
- …solid understanding of integration and partnering for Pharmaceutical development/ CMC with Quality , Regulatory, Operations, Non- clinical , Clinical , and other ... fast paced and contributes to the Pharmaceutical Sciences and Clinical Supplies (PSCS) deliverable which is the development of.../ our Research & Development Division ) such as Quality , Regulatory CMC, and technical functions, to ensure timebound… more
- Merck & Co. (North Wales, PA)
- …and vaccines for the benefit of patients and global human health.The Associate Vice President (AVP), Late Development Statistics, BARDS, is responsible and ... President in BARDS and will work collaboratively with other leaders in Clinical Development and Global Regulatory Affairs.--The AVP provides leadership and direction… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …responsible for the production of a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment. Job duties will be ... real-time floor service tasks (ie, kitting and kit cleaning, inventory management and data entry, sample management and data entry, aseptic behavior for cleaning… more
- IQVIA, Inc. (Durham, NC)
- …work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and ... in accordance with contracted scope of work and Good Clinical Practice. *Work with sites to adapt, drive, and...to manage ongoing project expectations and issues. *Evaluate the quality and integrity of study site practices related to… more
- Arrowhead Pharmaceuticals (San Diego, CA)
- …are collaborating to bring new therapies to patients in need. The Position The Clinical Research Associate (CRA) provides support to Study Lead(s) in clinical ... Support assigned study teams with TMF set-up, maintenance, ongoing quality control reviews, and final reconciliation of study documents...in clinical research 2 years as a Clinical Trial Associate ; study coordinator Proficient knowledge… more
- Ascension (Wichita, KS)
- …skills and competencies. Support clinical leaders in aggregating and interpreting various quality /patient safety data with a focus on using data to ... and Values encompass everything we do at Ascension. Every associate is empowered to give back, volunteer and make... clinical leaders in aggregating and interpreting various quality /patient safety data with a focus on… more
- Mount Sinai Hospital (New York, NY)
- Job Description The Clinical Research Associate I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities including ... Event Committee (CEC) meetings, if applicable. Identifies and documents data errors or items requiring clarification on all documents...studies as a clinical trial assistant or clinical research associate is highly desirable. About… more
- WorldLink (Mountain View, CA)
- …Monitors the study progress and creates sanity checklist to maintain high data quality . Operates and maintains physiological data collection ... Job Description TITLE: Clinical Research Associate (Digital Health) POSITION...data for physiological sensor measurements. Bachelor's Degree in Clinical Research, Engineering or Science Field (Engineering preferred). Understanding… more
- FocusKPI Inc. (Mountain View, CA)
- …Monitors the study progress and creates a sanity checklist to maintain high data quality . Operates and maintains physiological data collection laboratory ... FocusKPI is looking for a Clinical Research Associate to join one...3 Skills for an ideal person: Human subject research ( data collection on subjects, clinical research in… more
- Catalent, Inc. (Philadelphia, PA)
- … clinical packaging batch record operation. Responsible for safety, quality , production rates, material reconciliation, BRNRFT, and timelines adherence in the ... committed to a Patient First culture through excellence in quality and compliance, and to the safety of every...The Candidate Required a High School Diploma or Equivalent Associate degree highly preferred One+ year of clinical… more
