- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. JOB SUMMARYThe Director , Clinical Project Management will manage assigned project (s), including program's ... with agreed to development plans and corporate objectives. Advanced understanding of clinical research and the clinical drug development process Advanced… more
- Eisai, Inc (NJ)
- …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 to ... Salary Transparency Language:The base salary range for the Associate Director , Clinical Outsourcing is from :157,200-206,300Under current guidelines,… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …trial master file is complete and accurate for assigned stud(ies).If assigned, Associate Director , Clinical Operations may act as the Study Team Leader for ... and immune disorders.SummaryThe incumbent will be responsible for ensuring execution of clinical studies across geographic regions, in adherence to Good Clinical … more
- Merck & Co. (Rahway, NJ)
- …and procedures and-with quality standards internally and externally.Under the oversight of the CRD( Clinical Research Director ) / Director , Clinical ... or higher) with a strong emphasis in science and/or Clinical Research Management/ Administration .#MRLGCTO#eligibleforERPNOTICE FOR INTERNAL APPLICANTSIn accordance… more
- Eisai, Inc (Nutley, NJ)
- …to hear from you. Job Summary: As the Americas IT Security and Compliance Director , you play a pivotal role in ensuring the organization's adherence to security, ... Business Relationships:Promotes awareness of standards related to security, regulatory, clinical , commercial, and manufacturing processes to establish a culture of… more
- Merck & Co. (North Wales, PA)
- …in organization development and building a new team.Reporting to the Executive Director of CMC Integrated Project Management, the core responsibility of this ... to manage the Vaccines portfolio of products within CIPM. In addition, the Director will be expected to mentor/coach Project Managers (PMs) (through direct and… more
- Merck & Co. (Rahway, NJ)
- …to support the Animal Health division. The position reports to the Director , our company's Outcomes Research.Position objectives: To inform and contribute to the ... value evidence strategy and associated studies which describe clinical , economic, and patient-centered unmet needs and the value the product provides in addressing… more
- Eisai, Inc (NJ)
- …If this is your profile, we want to hear from you. The Medical Director , US Medical Affairs provides medical leadership for medical affairs strategy, planning and ... communication/publication components of overall medical operating plan. The Medical Director provides strategic development, planning, implementation and oversight of… more
- Eisai, Inc (Nutley, NJ)
- …your profile, we want to hear from you. Job Summary The Medical Director will provide medical leadership for medical affairs strategy, planning and supportive ... tactics for assigned therapeutic area. Under the direction of the Senior Medical Director , this role will be responsible for working with key stakeholders to develop… more
- Eisai, Inc (Nutley, NJ)
- …this is your profile, we want to hear from you.The Sr Medical Director provides medical leadership for medical affairs strategy, planning and supportive tactics ... communication/publication components of overall medical operating plan.The Sr Medical Director provides strategic development, planning, implementation, and oversight of… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …of analysis data sets and tables, listings, and figures (TLFs) needed for clinical study reports and regulatory submissions, as well as in-house validation of this ... workPossesses in-depth knowledge of regulatory authority's requirementsTypically has administrative responsibility for recruiting, retaining, developing, and managing employeesGuide… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …disorders. Summary The incumbent will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions, in adherence to Good ... Clinical Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food...(GCPs), appropriate Standard Operating Procedures (SOPs), Food and Drug Administration (FDA) regulations/EU Directive, and International Conference on Harmonization… more
- Tris Pharma (Monmouth Junction, NJ)
- …success.We have an immediate opening in our Monmouth Junction, NJ facility for a Director , Drug Safety. The Director , Drug Safety is responsible for planning, ... management planning. The incumbent works cross-functionally with counterparts/teams in Clinical Development, Regulatory Affairs, Manufacturing, Quality, etc. to identify,… more
- Catalent (Philadelphia, PA)
- Position: Director QualityLocation: Philadelphia, PAPosition Summary: The Quality function is to build, monitor, and sustain a robust and effective quality system ... good manufacturing practice/quality system requirements of the Food and Drug Administration , state boards of pharmacy, European, South American, Japanese, and… more
- Eisai, Inc (Nutley, NJ)
- …understanding of statistical methodologies and their application in the context of non- clinical studies and related projects in AD and other therapeutic areas as ... meet project deliverables and timelines within GV&A projects related to both clinical trial setting and observational studies.Serve as the lead statistician on… more
- Merck & Co. (Rahway, NJ)
- …a relevant discipline (eg, Outcomes Research, Health Economics, Epidemiology, Pharmaceutical Administration , Public Health, Health Policy, Medicine, or Clinical ... relevant discipline (eg, Outcomes Research, Health Economics, Epidemiology, Pharmaceutical Administration , Health Policy, Public Health) NOTICE FOR INTERNAL APPLICANTS… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …accredited college or university)- Bachelor's Degree required- Master's Degree Business Administration or Life Sciences preferred Experience- 7 or More Years ... Outsourcing, health sciences or related field ( clinical trials) required- 7 or More Years Deep experience in pharma procurement & category management required- CRO… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …of analysis data sets and tables, listings, and figures (TLFs) needed for clinical study reports and regulatory submissions, as well as in-house validation of this ... work. Possesses in-depth knowledge of regulatory authority's requirements.Typically has administrative responsibility for recruiting, retaining, developing, and managing employees.… more
- Eisai, Inc (Nutley, NJ)
- …describe complex disease processes to understand and evaluate the implications of clinical trials and real-world data; demonstrate the value of interventions beyond ... Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment… more
- Eisai, Inc (Exton, PA)
- …through phase 3, knowledge of the regulatory requirements at each stage of clinical development is essential.This position will have a direct impact on the success ... Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment… more
