- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Associate Clinical Research Manager (aCRM) - Oncology With support of other Clinical Research Manager's (CRMs) and/or ... Contact (POC) for assigned protocols and link between Country Operations and clinical trial team (CTT).Responsible for project management of the assigned studies:… more
- Eisai, Inc (NJ)
- …If this is your profile, we want to hear from you. Job Summary The Associate Director, Clinical Outsourcing, will oversee and lead and support activities related ... development.#LI-TS1Eisai Salary Transparency Language:The base salary range for the Associate Director, Clinical Outsourcing is from :157,200-206,300Under… more
- Eisai, Inc (Nutley, NJ)
- …is required.#LI-MI1#IND123#LI-RemoteEisai Salary Transparency Language:The base salary range for the Associate Director, Clinical Data Science - CEG is from ... your profile, we want to hear from you. The Clinical Data Science team at Eisai, Inc., is expanding...and big data analytics for the Oncology and Neurology clinical programs. This position will be focused on the… more
- Novo Nordisk Inc. (Atlanta, GA)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... difference? The Position Drives the understanding and delivery of quality clinical research (patient safety, rights and wellbeing; data reliability; scientific… 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 ... The Position Takes ownership to deliver upon near-term North America Clinical Development (NACD) goals, including successful delivery of studies within the… more
- Insmed Incorporated (Bridgewater, NJ)
- …and Best Workplaces for Millennials™ lists.OverviewAssist in the delivery of Clinical Operations objectives by providing operational support to the clinical ... study team (CST) with the responsibility to manage multiple clinical trials (all phases), and ensure compliance with SOPs, FDA regulations, GCP, ICH guidelines,… more
- Tris Pharma (Monmouth Junction, NJ)
- …needed and/or licenses or certificates preferred:Advanced degree (MS, MPH, PhD, PharmD, etc.) Clinical Research Associate (CRA) or Clinical Research ... Junction, New Jersey, Tris Pharma has an immediate opening for a Clinical Scientist/Grant AdministratorSUMMARY:The Clinical Scientist supports clinical … more
- The University of Vermont Health Network (Burlington, VT)
- …paid upon completion of one year of satisfactory service in the same department.The Clinical Care Associate (mirrors the Medical Assistant role in the specialty ... in direct patient care under the direction of a provider and performs clinical and administrative health care support services to patients and families according to… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …an equal opportunity employer including veterans and people with disabilities.SummaryThe Associate Director will be responsible for developing and implementing ... Clinical Pharmacology and Modeling & Simulation plans from FIH...FIH to post registration. Responsibilities include the development of Clinical Pharmacology and Modeling and Simulation plans, design and… 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 ... of the resources within NACD. Relationships Reports to Snr Director of Clinical Strategy and Business Operations within Operational Excellence and Delivery (OED).… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. ... documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to Clinical … more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …safety monitoring and risk management activities, provides insights on current clinical practice and guidelines, reviews and provides written assessments of relevant ... with board eligibility requiredExperience Qualifications1 or More Years of clinical experience preferredDaiichi Sankyo, Inc. is an equal opportunity/affirmative… 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)
- …existing and pipeline products to produce safe, effective, innovative medicine.The Global Clinical Data Standards Vocabulary Specialist, Associate Director, is a ... Job DescriptionOur Clinical Research and Pharmacovigilance team push the boundaries...boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- … clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good ... and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and other… more
- Merck & Co. (North Wales, PA)
- Job DescriptionOverview:The Associate Director Publication (Pub) Manager is the central source of information regarding publication activities and is responsible for ... and implementation of global publication strategies and tactical plans. The Associate Director Pub Manager oversees compliance with our company's publication… more
- Merck & Co. (North Wales, PA)
- …critical that our company receives consistent, accurate, high-quality data from clinical trials conducted worldwide. REAIM ( Risk Evaluation & Adaptive Integrated ... and central analytics and ensure exquisite oversight of our clinical trials. It is also business critical the integrity...of the System and Data Integration Lead (SDIL), the Associate SDIL is responsible for the integration between our… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …areas centered around rare diseases and immune disorders. Summary The Associate Director, Quantitative Systems Pharmacology (QSP) will work within the Quantitative ... Clinical Pharmacology (QCP) group to develop and apply QSP...include target prioritization, therapeutic modality selection, biomarker characterization and clinical trial design. In addition, he/she will develop a… more
- Merck & Co. (North Wales, PA)
- …to discover the next medical breakthrough.Position Description: The Associate Principal Scientist Statistical Programming leads the statistical programming ... activities for multiple and/or large/complex late stage drug/vaccine clinical development projects.- Accountability predominantly includes the development and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …opportunity employer including veterans and people with disabilities. Summary The Associate Director, External Data Management, is accountable for the end-to-end ... of External data in Daiichi Sankyo R&D collaborating with clinical and medical teams, clinical safety and pharmacovigilance, CROs and External Vendors for the… more
