- Merck & Co. (Rahway, NJ)
- …existing and pipeline products to produce safe, effective, innovative medicine.The Global Clinical Data Standards Vocabulary Specialist, Associate Director, ... for growth opportunitiesThe Vocabulary Specialist may lead or participate in:Internal clinical data standards forumsStandards development teams and data… more
- DivIHN Integration Inc (Columbus, OH)
- … data , medical and scientific data orally and in writing. Clinical Monitor or Research Coordinator Education: Associate or Bachelor's degree preferred in ... science undergraduate work for example. Skills: Some industry experience is desirable. Clinical knowledge to apply to adverse event data collection and/or… more
- Merck & Co. (Rahway, NJ)
- …to take center stage around the globe, timely completion of carefully designed clinical trials is critical to drug development.The Associate Director, ... The key areas of focus include: (1) diversity in clinical trials, (2) clinical trial recruitment and...clinical trials communications into strategic planning and priorities.Analyze data to enable greater awareness and understanding of how… more
- Merck & Co. (North Wales, PA)
- …(eg, database set up)Lead medical monitoring team in review and interpretation of clinical data /medical protocol deviations in collaboration with the Clinical ... and prioritization skills.Advanced analytical skills with the ability to interpret clinical trial data and synthesize conclusions.Interact with key stakeholders… more
- Novo Nordisk Inc. (San Antonio, TX)
- …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
- Merck & Co. (North Wales, PA)
- …and statistical analysis methods fundamental to effective pharmaceutical R&D.- The Clinical Safety Statistics (CSS) group within BARDS supports proactive assessment, ... Lead and provide statistical support for related drug/vaccine projects in Clinical Safety StatisticsInteract with Safety Physicians, Safety Scientists, Clinical … more
- Merck & Co. (Rahway, NJ)
- …as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites. Actively develops and ... expands the territory for clinical research, finding and developing new sites. Participates in...on-site monitoring & oversight activities using various tools to ensure: Data generated at site are complete, accurate and unbiased.Subjects'… 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
- 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 ... regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product development, CMR is involved. The… 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
- 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
- Tris Pharma (Monmouth Junction, NJ)
- …FUNCTIONS Actively participates in, or leads various aspects of preclinical or clinical data review including, but not limited to: adverse events, ... data management and safety management plans Ensures clinical data collection proceeds in a manner...licenses or certificates preferred:Advanced degree (MS, MPH, PhD, PharmD, etc.) Clinical Research Associate (CRA) or Clinical… more
- Merck & Co. (Rahway, NJ)
- …of decision-making at ouor 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 and… 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
- Legend Biotech USA, Inc. (Piscataway, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking an Associate Director Immuno-Oncology as part of the Research and Development team based ... of developing innovative cell-based therapies. We are seeking an experienced and dynamic Associate Director to lead our in vivo CAR-T cell therapy program. If you're… more
- Merck & Co. (North Wales, PA)
- … gaps and evidence needs.Assess and consider the impact of potential new clinical data and competitor developments on US access environment and strategy.Analyze ... Director, Pulmonary Arterial Hypertension (PAH) Payer Marketing & Access Strategy As Associate Director, PAH & Rare Disease Payer Marketing, you will be an… more
- Merck & Co. (North Wales, PA)
- …least 2 years of experience in publication managementUnderstanding of the clinical development process andclinical study data for assigned ... Job DescriptionOverview:The Associate Director Publication (Pub) Manager is the central...the selection of appropriate journals and congresses for scientific data dissemination. They work closely with both internal writing… more
- Merck & Co. (North Wales, PA)
- …systems and database expertise. Familiarity with statistical analysis methods and clinical data management concepts.US and/or worldwide drug or vaccine ... according to quality, compliance and timeliness requirements.-Expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO,… more
