- 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 interaction ... US and abroad, governmental, academic, community and industry organizations.The Senior Clinical Study Manager role is primarily...performance and quality metrics and share with study team, Operations Program Lead, and Sr . Director for… 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, ... 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
- Novo Nordisk Inc. (Stamford, CT)
- 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
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …PV Operations ' medical review function. This position supports a senior physician in evaluating and mitigating safety signals as they arise. Additionally, ... safety monitoring and risk management activities, provides insights on current clinical practice and guidelines, reviews and provides written assessments of relevant… 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
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …of clinical trial protocols. Provides medical and/or scientific direction to Clinical Operations . Represents Clinical Development on Project Teams. ... trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs.… more
- Merck & Co. (North Wales, PA)
- …with talented and dedicated colleagues while developing and expanding your career.The Senior Clinical Director ( Sr . Principal Scientist) has primary ... Our Company's Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the entire cycle… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …collaboration: Responsible for implementation of best practices and standards for clinical operations , including sharing lessons learned. Partner closely with ... management, placement and delivery to US and CA warehouses operations for US and CA Clinical Trial... Trial sites. Accountable for overall performance management of Senior Supply team, who contribute to the planning, execution… more
- Merck & Co. (Boston, MA)
- Job DescriptionThe Associate Vice President (AVP)/Therapeutic Area Head, Immunology Translational Medicine, will be responsible for leading the Translational ... Immunology strategy, bridging the continuum from Discovery Research through Late-Stage Clinical Development.-The AVP provides strategic oversight for the early … more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Vice President (AVP) will be responsible for leading the Translational Medicine (TMed) Cardiovascular & Respiratory Therapeutic Area and ... strategy, bridging the continuum from Discovery Research through Late-Stage Clinical Development.- The AVP provides strategic oversight for the early clinical … more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department At Novo Nordisk, our Finance and Operations team is the engine that elevates holistic commercialization of our products. The Finance and ... Operations team works closely with the business across the...and Market Research. The position has high exposure to senior management and requires a highly motivated individual who… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and drives execution for assigned projects in collaboration with GMA Clinical Operations and other cross-functional and regional stakeholders.Provides support ... research areas centered around rare diseases and immune disorders. Summary The Associate Director Global Medical Affairs Oncology (GMA), under the direction of the… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionDevice Development Associate Principal Scientist - Device Engineering and Early Development Lead ( Associate Director Equivalent)Our company's ... technical device development team(s) supporting individual drug assets currently in clinical development with line of sight to commercial filing and launch.… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …this position is accountable for partnering with the Global Team and Global Clinical leader to ensure effective team operations through meeting management, ... or regional project or be partnered with a more senior project manager in support of a larger, more...of these objectives. This position will report to the Sr . Director, Group Leader, GPM&L. Responsibilities Project Responsibilities: Independently… 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...across GCDS by actively communicating and proactively sharing informationSupport senior /leadership roles, in areas of observed competence, to enhance… more
- Catalent (Harman, WV)
- Senior Director, Supply Chain Position Summary: The Senior Director, Supply Chain is responsible for leading the supply chain organization for Catalent Maryland. ... suites coming online.Reporting to the Vice President and General Manager, the Senior Director Supply Chain directs all facets of supply chain management including,… more
- Merck & Co. (North Wales, PA)
- …Research & Division organization of our company.- Position Description/Summary: The GPAM Associate Director, Project Manager, is a core member of Early Drug ... the Research & Development pipeline and realize its full potential. The Associate Director is expected to provide project management leadership and drive… more
- Eisai, Inc (Nutley, NJ)
- …this is your profile, we want to hear from you.Job Summary:The Summer Associate (intern) will support Eisai's US Business Development & Established Products Group. ... and collaborations, as well as portfolio management of pharmaceutical brands. The associate will work in a cross-functional global organization and collaborate with… more
- Novo Nordisk Inc. (Boulder, CO)
- …the Department The Boulder Site is home to the specialized technical operations /CMC team for oligonucleotides and RNAi therapeutics, continuing its legacy as the ... process development, the CMC team works alongside Quality, Regulatory, Technical Operations and RNAi Early Development professionals at our Boulder, Colorado… more
- Sunrise System Inc (Atlanta, GA)
- Job Title: Sr . Associate , Aggregate Report Compliance Job ID: 24-02289 Location: Remote Duration: 12 months on W2 Contract. Notes from HM: Role can be 100% ... to spot if data is incorrect on report. Description: Sr . Associate , Aggregate Report Compliance In conjunction...partners, including: Office of the Chief Medical Officer (OCMO) Senior Leadership Team Office of the QPPV Global Regulatory… more
