- Merck & Co. (Rahway, NJ)
- …Interface with CROs to develop and analytically validate genetic biomarker assays to support clinical programs. Oversee and/or support results reporting and ... external R& D collaborations to enable innovative strategies for clinical trial biomarker testing. Author and review...with the use of minimal residual disease assays to support clinical studies Deep understanding of disease… more
- Merck & Co. (Rahway, NJ)
- …as the GCS spokesperson at clinical development related meetings (ie, Clinical Trial Teams) and product-development related meetings. The incumbent must have ... development teams and the operational/executional arms within the business .- - Working independently, the Protocol Clinical ...limited to: Participates as a key stakeholder on the Clinical Trial Teams (CTT) and collaborates closely… more
- Merck & Co. (Rahway, NJ)
- …- Primary activities include, but are not limited to: - Participates on the Clinical Trial Team (CTT) and collaborates closely with other functional area ... etc.) as well as other organizations such as Global Clinical Trial Operations (GCTO) Regional colleagues and...consolidated forecast for CFGs is maintained. - - Report clinical supply chain incidents to support the… more
- Merck & Co. (Rahway, NJ)
- … Research, Clinical Trial Planning, Clinical Trials, Clinical Trial Support , Cross-Functional Teamwork, Documentations, Drug Development, Ethical ... for investigational or marketed cardiovascular and respiratory drugsAnalyzing and summarizing clinical findings from studies to support decisions regarding… more
- Merck & Co. (MA)
- …early clinical development plan and Investigational New Drug applications.Providing clinical development support of business development assessments of ... clinical trials for investigational drugs.Analyzing and summarizing the clinical findings from studies to support decisions... Clinical Medicine, Clinical Research Management, Clinical Studies, Clinical Trial Development,… more
- Merck & Co. (Boston, MA)
- …Atherosclerosis, Cardiology Clinical Research, Cardiovascular Diseases, Clinical Development, Clinical Studies, Clinical Trial Designs, Clinical ... trials for investigational or marketed Atherosclerosis drugsAnalyzing and summarizing the clinical findings from studies to support decisions regarding safety… more
- Merck & Co. (Upper Gwynedd, PA)
- … Clinical Judgment, Clinical Medicine, Clinical Reporting, Clinical Research Management, Clinical Trial Development, Communication, Data Analysis, ... Director may be responsible for: -Analyzing and summarizing the clinical findings from studies to support decisions...with external researchers around the world; Travel on company business about twenty (20) percent of the time to… more
- Genmab (NJ)
- …SAS programming, 6-8 years experience. Practical knowledge and experience using R to support clinical trial preferred Demonstrated knowledge of clinical ... in a multi-study, multi-disciplinary atmosphere in a matrix environment Experience in clinical data management and/or trial management experience with technical… more
- Merck & Co. (North Wales, PA)
- …for the formulation and execution of automation strategy in Global Clinical Trial Operations and all the support activities within their functional area. ... This includes working with stakeholders across Global Clinical Trial Operations (GCTO)and other relevant teams, driving the strategy from ideation to value… more
- Genmab (NJ)
- …within Genmab, the Site Engagement Manager role will bring a high-touch and clinical trial 'face' with our sites.Additionally, the Manager may also ... support on-site and/or remote trial oversight activities...data.Responsibilities/tasks:The site engagement representative is expected to forge strong clinical trial related relationships with Genmab sites,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …acquisition, validation, and reconciliation, study data protection, operational metrics, and clinical trial quality and risk management reporting requirements ... acceptance and reconciliation reports, study data protection, operational metrics, and clinical trial quality and risk management reporting requirements.Oversees… more
- Merck & Co. (Rahway, NJ)
- …data management; a general understanding of worldwide regulatory requirements; and with good clinical trial experience in Phase II/ III trials.- The knowledge ... principles and statistical methods applied to designing and analyzing clinical trials in support of worldwide regulatory...clinical trials and coordinating the statistical activities for clinical trial projects; and may lead a… more
- Merck & Co. (Rahway, NJ)
- …or related field plus 9 years SAS programming experience in a clinical trial environment.MS in Computer Science, Statistics, Applied Mathematics, Life ... for the design and maintenance of statistical datasets that support multiple stakeholder groups which include clinical ...7 or more years SAS programming experience in a clinical trial environment. Department Required Skills and… more
- Genmab (NJ)
- …statistical analysis plans, results meetings presentations and clinical trial reportsCoordinate data transfers from/to business partners in collaboration ... families and employees.Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly… more
- Genmab (NJ)
- …statistical analysis plans, results meetings presentations and clinical trial reportsCoordinate data transfers from/to business partners in collaboration ... capabilityExperience in statistical analysis, modelling and simulation and adaptive trial designsExperience in working with clinical trialsPreferred experience… more
- Merck & Co. (Rahway, NJ)
- …identifying and implementing novel quantitative approaches (for eg, comparator modeling, clinical trial simulations,- quantitative system pharmacology (QSP) and ... and productive interactions among diverse personalities/areas of expertise#QP2#EligibleforERPRequired Skills: Clinical Trial Designs, Clinical Trial… more
- Merck & Co. (Rahway, NJ)
- …or related field plus 5-9 years SAS programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life ... or related field plus 3-7 years SAS programming experience in a clinical trial environment Department Required Skills and Experience: Effective interpersonal… more
- Eisai, Inc (Woodcliff Lake, NJ)
- …3 years MSL experience in Oncology/Hematology.Strong broad-based scientific and pharmaceutical knowledge. Clinical trial development and drug launch experience is ... Area Support to External Stakeholders Act as the primary clinical /scientific resource to Healthcare Providers (HCPs) in the territory for information pertaining… more
- Merck & Co. (North Wales, PA)
- …Sciences, Engineering or related field plus 5 years SAS programming experience in a clinical trial environmentOR a master's degree (or US equivalent) in Computer ... Engineering or related field plus 3 years SAS programming experience in a clinical trial environment. Requirements: Experience in US and/or worldwide drug or… more
- Merck & Co. (North Wales, PA)
- …Engineering or related field plus 5 years SAS programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life ... for the design and maintenance of statistical datasets that support multiple stakeholder groups which include clinical ...field plus 3 years SAS programming experience in a clinical trial environment- Department Required Skills and… more
