- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …(FDA) regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines.The Senior Clinical Study Manager will have routine ... subsidiaries in the US and abroad, governmental, academic, community and industry organizations.The Senior Clinical Study Manager role is primarily a… more
- Merck & Co. (North Wales, PA)
- …and presentation skillsEducation/Experience: Bachelor's Degree +5 years of pharmaceutical, clinical drug development, project management, and/or medical field ... experience OR Master's Degree +3 years of pharmaceutical, clinical drug development, project management, and/or medical field experience OR PhD/PharmD… more
- Merck & Co. (Rahway, NJ)
- …executing end to end Data Management activities with the support and oversight of a Senior Clinical Data Manager (SCDM)/Lead Clinical Data Manager ... project assignments under the direction of an Operations Manager (OM). - Your Fellowship Project -...Fellowship - Mentoring & networking opportunities within and beyond Clinical Trial Operations Exposure to Senior level… more
- Merck & Co. (North Wales, PA)
- …Word, Outlook, etc.)Education/Experience:Bachelor's Degree +5 years of pharmaceutical, clinical drug development, project management, and/or-medical field ... experienceOR Master's Degree +3 year of pharmaceutical, clinical drug development, project management, and/or-medical field experienceOR PhD/PharmD DegreeDegree… more
- Merck & Co. (North Wales, PA)
- Job DescriptionPosition Description: Senior Study Manager - Epidemiology OperationsSupport the Lead Epi Scientists by providing overall operational support for ... Operating Procedures (SOPs). Manages several complex activities and study types.Our Clinical Research and Pharmacovigilance team push the boundaries of global… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders.Summary The Clinical Trial Information Disclosure Manager leads company operational activities ... the WHO, IFPMA, and EFPIA-PhRMA principles. A member of the Global Clinical Trial Disclosure Platform and Operations Committee. Facilitates the company's compliance… more
- Merck & Co. (Rahway, NJ)
- …training and operational project assignments under the direction of Lead Clinical Scientist and Lead Study Manager . Your Fellowship ProjectYou will partner ... & networking opportunities within and beyond CSSM Exposure to Senior level positions within the clinical development...forum Hands-on experience in the conduct and execution of clinical trials Development of critical analysis and project… more
- Eisai, Inc (NJ)
- …If this is your profile, we want to hear from you. Job Summary The Senior Manager , Medical Writing will be the designated Lead Medical Writer for approximately ... system#LI-HC1#IND-123Eisai Salary Transparency Language:The base salary range for the Senior Manager , Medical Writing is from :126,300-165,800Under current… more
- Merck & Co. (Durham, NC)
- Job DescriptionThe Quality Senior Specialist provides expertise in the coordination of resources and equipment pertaining to qualification/validation activities ... supporting the vaccine expansion facility. Primary Responsibilities: The Quality Senior Specialist will be responsible for comprehensive management of all activities… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …or related role in a biotech or pharmaceutical companyDemonstrated success as a project manager /leader in planning and executing strategies for global drug ... rare diseases and immune disorders.SummaryThis position is responsible for providing project management, drug development expertise to Global Project Teams… more
- Merck & Co. (Rahway, NJ)
- …training and operational project assignments under the direction of Lead Clinical Scientist and Lead Study Manager . Your Fellowship ProjectYou will partner ... & networking opportunities within and beyond CSSM Exposure to Senior level positions within the clinical development...forum Hands-on experience in the conduct and execution of clinical trials Development of critical analysis and project… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and leads/contributes to internal statistical workstreams to address various project needs. The position works closely with contract research organization ... review), Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Executes statistical activities for low to… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Interaction & Collaboration level: Requires interaction with vendors and key senior stakeholders at Sr manager and director level in ... other research areas centered around rare diseases and immune disorders. Summary: Manager , Sales Training and Development - Oncology serves as the training subject… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …as well as other research areas centered around rare diseases and immune disorders.Summary The Manager / Senior Manager , Data Programmer is a member of the ... to support drug development processes and global submissions as required for clinical trials. These include developing and validating SAS programs for clinical… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …organization and will work regularly with all business areas (Sales, Marketing, Clinical , TMPC, Med Affairs, and Regulatory Affairs) and support functions (IT, ... etc., under the direction of Director, Compliance Policy, Training and Communications. Project manage various teams to build creative training programs from… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …areas centered around rare diseases and immune disorders. Summary The Regulatory Data Manager will be a key member of the Global Regulatory Affairs (GRA) Process ... As a result, this role will need to partner closely with teams and senior leaders from across Regulatory Affairs, as well as cross-functional stakeholders (eg, RA… more
- Novo Nordisk Inc. (Durham, NC)
- …processes in accordance with relevant project plans & timelines. Relationships Senior Manager , Quality Control - OFP. Essential Functions Accuracy & ... minimum of three (3) years of experience in a clinical or industrial/pharmaceutical laboratory May consider a High School...minimum of five (5) years of experience in a clinical or industrial/pharmaceutical laboratory Minimum of one (1) year… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …diseases and immune disorders. Summary The Global Team Leader, is a senior , cross-functional leader in Daiichi Sankyo's Global R&D organization. At Daiichi Sankyo, ... the engine of development is the cross functional, empowered and agile Global Project Team (GPT), directly accountable to global Development governance. In this key… more
- Catalent (St. Petersburg, FL)
- …of process controls in all applicable areas of the manufacturing operation. The Senior QA Specialist will assist in organizing and prioritizing the activities and ... is responsible for actively identifying compliance enhancements/improvements and leading project to deliver solutions. Furthermore, this position will participate in… more
- Magellan Health Services (Albuquerque, NM)
- …financial analysis. Extensive Knowledge of Microsoft suite of tools. General Job Information Title Senior Clinical Project Manager Grade 28 Work ... clinical operations, quality, network, and 5+ years in project management. Bachelors of Science in Nursing, Masters in...Experience - Required Clinical , Network, Project /Program Management, Quality Work Experience - Preferred Education -… more
