- Merck & Co. (Rahway, NJ)
- …Qualifications: Education Minimum Requirement: BA/BS required with strong emphasis in science and/or biology.Min. 2 years of clinical research experience. ... Job DescriptionPosition Description: Associate Clinical Research Associate - Northeast Region (Remote) With...and patient recruitmentDeveloping level of monitoring skill and independent professional judgment.Good IT skills (Use of MS office, use… more
- Merck & Co. (Rahway, NJ)
- …organizational policies and practices.Requirements:B.A./BS required with strong emphasis in science and/or biology.-Min. 2 years of clinical research ... Job DescriptionWith support of Sr CRA ( Clinical Research Associate) and/or CRA Manager, acts as...performance-and patient recruitmentDeveloping level of monitoring skill and independent professional judgment.Good IT skills (Use of MS office, use… more
- Merck & Co. (Rahway, NJ)
- …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 internal...patient recruitment.Demonstrated high level of monitoring skill with independent professional judgment.Good IT skills (Use of MS office, use… more
- Merck & Co. (North Wales, PA)
- …relies on accurate data collected from patients who are part of Clinical Trials. Trial Standards, Trial Design, Trial Data Collections, Trial Data Integrations, ... trial participants, in the right way to enable the Clinical Research to analyze data for efficacy, dosing, safety...dedicated to this important capability.We are looking for a professional with strong analytical skills and experience in the… more
- Merck & Co. (Rahway, NJ)
- …improve lives. -Position Description: Under the guidance of the Oncology Clinical Development Finance Associate Director, the Finance Senior Specialist will:Provide ... and analytical support to our Research & Development Division Oncology Clinical DevelopmentForecast grant spend as well as provide financial support related… more
- Tris Pharma (Denton, TX)
- …products spanning neuroscience and other therapeutic categories employing our proprietary science and technology.Our science and technology make us unique, ... believe in one another and we believe in respectful, open and honest communications to help support individual and...limited to: generating sales, communication and promotion of the clinical and economic benefits of the product, building and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …negotiations in accordance with all relevant regulations and policies; (Good Clinical Practice (GCP), ICH guidelines, federal regulations (Sunshine/ Open Payments ... leads, and effectively interfaces within a matrixed environment and with varying professional levels Leads Clinical Ancillary Management project teams to ensure… more
- Merck & Co. (Rahway, NJ)
- …first-hand - one of strong ethics & integrity, diversified experiences, exceptional science and a resounding passion for improving human health through innovative ... development as well as for the release and shelf-life assessment of clinical materials. - Troubleshoot challenges associated with drug development through active… more
- Merck & Co. (North Wales, PA)
- …or related field plus 5 years SAS programming experience in a clinical trial environment.MS in Computer Science , Statistics, Applied Mathematics, Life ... statisticians and other project stakeholders.Primary Activities:Programmatically synthesize preclinical / clinical data into analysis ready structures from varied data… more
- Merck & Co. (North Wales, PA)
- …of 9 years Statistical Analysis System (SAS) programming experience in a clinical trial environment. MS (preferred) in Computer Science , Statistics, Applied ... programming activities for multiple and/or large/complex late stage drug/vaccine clinical development projects.- Accountability predominantly includes the development and… more
- Merck & Co. (Rahway, NJ)
- …in the role of Associate Director QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to ... clinical pharmacology and pharmacometrics of oncology drugs from post-PCC...and statistics.Proficiency in R, NONMEM or other similar programing language. Professional working proficiency in written and verbal communication."This (remote)… more
- Merck & Co. (Rahway, NJ)
- …activities for multiple and/or large/complex late stage drug/vaccine clinical development projects.- Accountability predominantly includes the development and ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… more
- Merck & Co. (Rahway, NJ)
- …(PK) and pharmacodynamics (PD) analysis, model-based meta-analysis (MBMA), clinical trial simulations (CTS), disease progression modeling and Artificial ... to drive portfolio impact. Please note, this position is open to remote work. To comply with applicable law,...seek to improve cycle time, cost/size, number of trials, clinical trial design and Go/No Go decisions- Serve as… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Degree or other advanced degree preferred Experience Qualifications10+ years of professional experience in regulated activities, clinical development and QA ... Clinical DevelopmentMust possess a profound understanding of the science of product developmentDemonstrated accomplishments working within a global/matrix… more
- Tris Pharma (Monmouth Junction, NJ)
- …products spanning neuroscience and other therapeutic categories employing our proprietary science and technology.Our science and technology make us unique, ... we interact with one another. We believe in each other and in respectful, open and honest communications to help support individual and team success.We have an… more
- Merck & Co. (Rockville, MD)
- …support for our causes and maintaining a strong reputation as a science -led biopharmaceutical leader.- We work in partnership with the company's Research ... Laboratories divisions and most directly with Global Regulatory Affairs and Clinical Safety (GRACS) to define and implement a prioritized plan for policy that… more
- Merck & Co. (North Wales, PA)
- …or related field and at least 5 years SAS programming experience in a clinical trial environment orMS in Computer Science , Statistics, Applied Mathematics, Life ... This position supports statistical programming activities for late stage drug/vaccine clinical development projects. This may include leadership of one or more… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 120 years of scientific expertise and ... sharing best practices, providing coaching and feedback, and supporting the professional development of team members. Additionally, actively foster a culture of… more
- Merck & Co. (Rahway, NJ)
- …first-hand - one of strong ethics & integrity, diversified experiences, exceptional science and a resounding passion for improving human health through innovative ... analy sis. You would also contribute towards regulatory submissions to enable clinical trials. Your main responsibilities include: - Driving solutions to analytical… more
- Merck & Co. (Rahway, NJ)
- …data analysis. You would also contribute towards regulatory submissions to enable clinical trials. Your main responsibilities, which are in no particular order and ... as well as methods for the release and shelf-life assessment of clinical supplies under good manufacturing practice (GMP) settings.Author investigational new drug… more
