- Arthrex (Naples, FL)
- …studies to contribute to advances in the medical community. Experience as a clinical research professional and knowledge of clinical regulatory regulations ... full time employees.**This position is based in Naples, FL. Open to remote for the right candidate. If remote,...related field are required for success in this position. Clinical Research Professional certification is also strongly… 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
- Merck & Co. (Rahway, NJ)
- …professional image and competitive advantage through patents, presentations, publications and professional activities and advance areas such as science and ... Job DescriptionOur company's Pharmaceutical Sciences & Clinical Supplies organization translates molecules to medicines, working from the discovery interface through… more
- Merck & Co. (Rahway, NJ)
- …biopharmaceutical company.- Our Company Research Laboratories ( drive break-through science through drug discovery, development and clinical evaluation ... business.Under the guidance of the Director, Pharmaceutical Sciences and Clinical Supply (PSCS), this position is accountable for providing comprehensive… 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
- 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
- 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. (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
- 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)
- …first-hand - one of strong ethics & integrity, diversified experiences, exceptional science and a resounding passion for improving human health through innovative ... You would also contribute towards regulatory submissions to enable clinical trials.Your main responsibilities include: Driving solutions to analytical development… 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
- 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. (Los Angeles, CA)
- …engage and train internal employees to ensure that they thoroughly comprehend the science behind the medicine and review further unmet medical needs to bolster ... and/or sharing of therapeutic expertise.Responsibilities and Primary ActivitiesScientific ExchangeDevelops professional relationships and engages with national and regional SLs… 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
- Merck & Co. (North Wales, PA)
- …and regionsServes as an impactful member of Product Development Team sub-teams ( Clinical , Value Evidence, Commercial, Publications and Label) and Global Human Health ... public groups, government officials, medical societies) about Our Company's emerging science .Organizes global expert input events (advisory boards and expert input… more
- Merck & Co. (Rahway, NJ)
- …(small molecule, macrocyclic peptides, bioconjugates) Drug Substance development and GMP clinical manufacturing plant currently planned in Rahway, New Jersey. The ... is to serve as PR&D's internal node for small molecule drug substance clinical manufacture, and as preferred site for first pilot of commercial small molecule… more
- Marion County (Salem, OR)
- …degreein a social science field, and five (5) years of responsible, professional experience in the mental health system, including three (3) years in a ... has been reopened for additional applicants and will remain open until filled. If you have already applied for...that support our department mission. A commitment to excellent clinical quality to the population we serve and ability… more
Related Job Searches:
Clinical,
Clinical Science,
Clinical Science Professional,
Open,
Professional,
Science