- Merck & Co. (Rahway, NJ)
- … trial team.Leading medical monitoring team in review and interpretation of clinical data /medical protocol deviations in collaborations with the Clinical ... in collaboration with Data Management/Programming.Collaborating cross-functionally to monitor clinical data to ensure quality, completeness, and integrity of… more
- Merck & Co. (Rahway, NJ)
- … Senior Director will manage the entire cycle of clinical development, including study design, initiation, execution,-monitoring, analysis, regulatory reporting, ... will interact externally with key opinion leaders. Specifically, the Senior Director May Be Responsible For: Evaluating pre- clinical... Clinical Research Management, Clinical Studies, Clinical Testing, Clinical Trials, Data … more
- Merck & Co. (Rahway, NJ)
- …marketed Oncology medicines. Our company's oncology medicines span all phases of clinical development (pre- clinical to post-licensure).The Senior Director ... placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Senior Director may be responsible for:Evaluating pre- clinical and… more
- Merck & Co. (Rahway, NJ)
- … Senior Director will manage the entire cycle of clinical development, including study design, initiation, execution, monitoring, analysis, regulatory reporting, ... and publication.Specifically, the Senior Director may be responsible for:Evaluating pre- clinical ... Clinical Testing, Clinical Trial Development, Clinical Trials, Communication, Data Analysis, Drug Development,… more
- Genmab (NJ)
- …regional, national, and global Medical Affairs strategiesProvide insights/feedback on emerging scientific/ clinical data that enhance the value and appropriate ... RoleGenmab is currently seeking a Hematology Medical Science Liaison (MSL)/ Senior MSL ( Sr . MSL) to be a...exchange in a fair and balanced manner and provide clinical /scientific support for Genmab's pipeline.Domestic travel of approximately 50%… more
- Merck & Co. (North Wales, PA)
- …be programmed; an understanding of statistical terminology and conceptsFamiliarity with clinical data management conceptsExperience in CDISC and ADaM ... Specific Required Skills and Experience: Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH;… more
- Eisai, Inc (Nutley, NJ)
- …we want to hear from you. Job Summary The Medical Science Liaison (MSL) / Senior Medical Science Liaison ( Sr . MSL) is a field-facing representative of US Medical ... participate in scientific exchanges and interactions with identified KOLs.Present clinical , scientific and economic data on Eisai's...salary range for the Medical Science Liaison (MSL) / Senior Medical Science Liaison ( Sr . MSL), Oncology… more
- Eisai, Inc (Nutley, NJ)
- …the workforce to evolving technologies.Align clinical portfolio, business strategy, clinical studies, and related functions eg data management, clinical ... capacity, preferred.Significant experience working in multifunctional environments and influencing senior stakeholders using data .Strong performance in earlier… more
- Eisai, Inc (Boston, MA)
- …coverage efforts, including coordination of all MSL activities, as required. Present clinical , scientific and economic data on Eisai's products and relevant ... Territory Management (MSL)Eisai Salary Transparency Language:The base salary range for the Senior Medical Science Liaison ( Sr . MSL) / Principal Medical Science… more
- Eisai, Inc (Los Angeles, CA)
- …coverage efforts, including coordination of all MSL activities, as required. Present clinical , scientific and economic data on Eisai's products and relevant ... Territory Management (MSL)Eisai Salary Transparency Language:The base salary range for the Senior Medical Science Liaison ( Sr . MSL) / Principal Medical Science… more
- Merck & Co. (Upper Gwynedd, PA)
- …medicines. Our Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the entire cycle ... compounds and the further study of marketed compounds. In executing these duties, the Senior Director may: Supervise the activities of Clinical Scientists in the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …as other research areas centered around rare diseases and immune disorders. SummaryThe Senior Director of Clinical Operations will manage clinical operations ... the effective and efficient execution of operational aspects of clinical study planning, implementation, data delivery and...operational and overall delivery and tactical execution of the clinical studies. The senior director will ensure… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Job Summary: The Sr . Director, Clinical Safety MD, will lead the development and ... and serving as the primary point of contact.Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification… more
- Merck & Co. (Rahway, NJ)
- …In particular this will include developing and maintaining a profound knowledge of Good Clinical Practice with respect to digital data management (ie use of ... Management, Clinical Study Design, Clinical Trial Planning, Clinical Trials Monitoring, Communication, Data Analysis, ICH GCP Guidelines, Management… more
- Merck & Co. (San Diego, CA)
- …Arrangements:Not ApplicableShift:1st - DayValid Driving License:YesHazardous Material(s):NoRequired Skills:Adaptability, Clinical Data , Clinical Operations, ... outcome assessments, biomarker sample collection and management, and external data monitoring committee for ophthalmology clinical trials.Experience in managing… more
- Merck & Co. (Rahway, NJ)
- …Skills:Adaptability, Bioreactors, cGMP Regulations, Chemical Engineering, Chromatographic Techniques, Clinical Judgment, Communication, Data Analysis, Design of ... synthesis and wet chemistry including running experiments, and generating and analyzing data - Familiarity with Process Analytical Technologies (PAT) and/or data… more
- Merck & Co. (Rahway, NJ)
- …Under the guidance of dCMC Regulatory A uthoring L eadership , t he Senior Specialist, Regulatory Authoring Data Analyst, will o ptimize regulatory authoring ... initiative that will enable the pipeline by establishing a digital continuum of data from development through manufacturing for our products and processes .- dCMC… more
- Eisai, Inc (Pittsburgh, PA)
- …If this is your profile, we want to hear from you. The Senior Oncology Sales Specialist is responsible for meeting/exceeding sales goals through promoting Oncology ... within an assigned territory in a compliant and appropriate manner. The Senior Oncology Sales Specialist represents and promotes assigned brand(s) in the oral… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …by utilizing the Spend Per Audit and Spend Per Participant Reports. Audit data against supporting documentsReview all receipts for compliance and accuracy and that ... ( ie F&B receipt, AV, sign in sheet, etc.)Run agg spend data reporting for each meeting.Review findings with ManagerAddress any inconsistencies and concerns… more
- Merck & Co. (North Wales, PA)
- …Management Office (PMO); and Administrative Professionals.Position Description/Summary The GPAM Senior Specialist, Value & Implementation Project Manager (VIPM), is ... to progress the R&D pipeline and realize its full potential. The Senior Specialist is expected to provide project management leadership and drive cross-functional… more
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