- Jazz Pharmaceuticals (Palo Alto, CA)
- …please visit www.jazzpharmaceuticals.com and follow @JazzPharma on Twitter. Brief Description:The Associate Director, Clinical Data Innovation is responsible ... an enterprise business intelligence application that utilizes AWS and TableauThe Associate Director, Clinical Data Innovation will lead a team of… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Associate Clinical Research Associate - Northeast Region (Remote) With support of Senior Clinical Research ... primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites.Develops strong site relationships… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …are achieved according to agreed quality standards and timelines and that quality of data is suitable for regulatory submission. The Associate Director will have ... trial master file is complete and accurate for assigned stud(ies).If assigned, Associate Director, Clinical Operations may act as the Study Team Leader for the… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionWith support of Sr CRA ( Clinical Research Associate ) and/or CRA Manager, acts as primary site contact and site manager-throughout all phases of a ... clinical research study, taking responsibility of allocated sites.Develops strong...on-site monitoring & oversight activities using various tools to ensure: Data generated at site are complete, accurate and unbiasedSubjects'… more
- Novo Nordisk Inc. (Los Angeles, CA)
- …a difference? The Position Drives the understanding and delivery of quality clinical research (patient safety, rights and wellbeing; data reliability; scientific ... relevant regulatory requirements Ensure accuracy, validity and completeness of data collected at clinical trial sites in...validity and completeness of data collected at clinical trial sites in accordance with the protocol, Monitoring… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …a difference? The Position Drives the understanding & delivery of quality clinical research (patient safety, rights & wellbeing; data reliability; scientific ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...with the FDA to providing medical education and collecting data to support efficacy and new product development, CMR… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …to ensure appropriate biomarker, PK / PD measurements; Reviews emerging clinical data regularly; Leads dose-escalation meetings; Performs quality assessment ... trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs.… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …SDTM and industry standard data collection practices preferred- 7+ years Clinical data management experience in a medical device, pharmaceutical company, or ... equal opportunity employer including veterans and people with disabilities. Summary The Associate Director, External Data Management, is accountable for the… more
- Merck & Co. (North Wales, PA)
- …ability to work independently in a global setting.Microsoft Office and data analytics proficiencyPreferred:Prior work experience in clinical outcome assessment ... of our company's diverse development portfolio comprising over 200 clinical trials in compliance with global and local regulations....of relevant experience in the pharmaceutical industry or an Associate 's Degree with a minimum of 5 years of… more
- Merck & Co. (North Wales, PA)
- Job DescriptionPosition Description: Specialist, Clinical Operations Global Clinical Trial Operations (GCTO) is a global organization operating in over 50 ... the delivery of our company's diverse development portfolio comprising over 200 clinical trials in compliance with global and local regulations. The Regional… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and immune disorders. Summary Position manages the end-to-end delivery of data management services for assigned projects/studies, collaborating with CROs and other ... development processes and global submissions. This position provides leadership within Data Management by partnering with internal and external stakeholders to… more
- Merck & Co. (Rahway, NJ)
- …Quantitative Pharmacology and Pharmacometrics - Immune/Oncology (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global Clinical ... organization and has oversight over drug development aspects related to clinical pharmacology and pharmacometrics of oncology drugs from post-PCC to registration.… more
- Merck & Co. (Rahway, NJ)
- …of our Research & Development Division is seeking applicants for an Associate Principal Scientist position available at its Kenilworth, New Jersey research ... facility.- The Associate Principal Scientist is a laboratory-based scientific role tasked with solving complex analytical problems at the interface of biology,… more
- Merck & Co. (Rahway, NJ)
- …and validation of flow cytometric assays that are deployed in support of clinical trials. The candidate for this Associate Principal Scientist position should ... Molecular Biomarkers (TMB) is responsible for translating preclinical molecular biomarkers to clinical development across all therapeutic areas and all phases of … more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... with the FDA to providing medical education and collecting data to support efficacy and new product development, CMR...This includes leading processes and technology improvements to link Clinical trial site needs, Finance and Supply forecasts that… more
- Merck & Co. (Rahway, NJ)
- …systems and database expertise. Familiarity with statistical analysis methods and clinical data management concepts.US and/or worldwide drug or vaccine ... Job DescriptionThe Associate Principal Programmer leads the statistical programming activities...to quality, compliance and timeliness requirements.-Expertise in SAS and clinical trial programming including data steps, procedures,… more
- Merck & Co. (Boston, MA)
- …(PDMB) group is seeking a dynamic, strategic thinking and collaborative Associate Principal Scientist to contribute to our company's protein therapeutic drug ... discovery and early clinical development efforts. -This position will be based at...teams through generation and interpretation of PK and PK/PD data as well as through effective communication at both… more
- Merck & Co. (Rahway, NJ)
- …of decision-making at our company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas.This Associate ... PK/PD models, exposure response (ER) models, model-based meta-analysis (MBMA), clinical trial simulations (CTS) and disease progression modeling into programs… more
- Merck & Co. (North Wales, PA)
- …from MI capabilities to inform strategic planning and identify gaps in data and educate on scientific exchange for appropriate stakeholders. Staff medical ... via initiatives, mentoring, process improvements, and/or innovationsStrong knowledge of clinical trial methodology, statistical concepts, and evaluation and interpretation… more
- Merck & Co. (Rahway, NJ)
- …reliance on automation within Biologics Process Research & Development (BPR&D).The Associate Director role-will provide process automation leadership within the BDC ... automation activities throughout the facility.-Primary Responsibilities:Provide process support for clinical manufacturing and R&D processes while also facilitating tech… more
