- JENAVALVE TECHNOLOGY INC (Irvine, CA)
- …Level 4 Year Degree Salary Range $120000.00 - $130000.00 Salary Description Job Title : Manager , Clinical Affairs (Case Review Board) Manager Title: ... Director, Clinical Affairs Job Description Summary: Reporting to the Director of Clinical Affairs, the Manager , Clinical Affairs (CRB) will be… more
- Insmed Incorporated (NJ)
- …each other, and for the future of science, we're in. Are you?About the Role:The Clinical Trial Manager will be responsible for the management and oversight of ... Clinical Scientist, Clinical Indication/Development Lead, and clinical study team to ensure ongoing review ...and clinical study team to ensure ongoing review of patient profiles and data listings.Proactively identifies potential… more
- Merck & Co. (Rahway, NJ)
- …Management Section of the GCS Planning organization.- Working independently, the Inventory Manager Clinical Supplies Project Manager (IM CSPM) creates ... supply chain deliverables and prepares, analyzes, and/or develops mitigation strategies for review with clinical partners and senior leaders. - Responsible and… more
- Merck & Co. (Rahway, NJ)
- …operational/executional arms within the business.- - Working independently, the Protocol Clinical Supplies Project Manager (Protocol CSPM) designs strategic and ... supply chain deliverables and prepares, analyses, and/or develops mitigation strategies for review with clinical partners and senior leaders. Works directly in… 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 ... vendor related activities in Patient Safety including, but not limited to contract review and vendor management support in regard to safety reporting. To serves as… more
- Insmed Incorporated (NJ)
- …patients with serious diseases. In this role, you'll be reporting to the Sr. Manager , Clinical Supply Chain & Logistics.The Insmed Summer Internship Program is ... About the Role:We're looking for a Summer Intern - Clinical Supply Chain & Logistics on the Logistics to...you'll have the opportunity to be responsible for the review and development of process improvement strategies/documents to build… more
- Insmed Incorporated (NJ)
- …CSV plans Provide real-time oversight and support during test execution and review executed protocols Provide operational support in maintaining systems in a ... in the CSV SharePoint site, managing CSV documents in Veeva, routing documents for review and approval in Veeva etc. This role will also provide CSV oversight in… more
- Insmed Incorporated (San Diego, CA)
- …Gdoc. Etc.) Provide real-time oversight and support during test execution Review executed protocols and provide test protocol deviation assessment and resolution ... in the CSV SharePoint site, managing CSV documents in Veeva, routing documents for review and approval in Veeva etc. This role will participate in on site Change… more
- Novo Nordisk Inc. (Boston, MA)
- …functionally with multiple functions and groups throughout the US organization, Clinical Development, Research & Early Development, other affiliates, and the Global ... a leader in the rare endocrine marketplace. The Rare Endocrine Therapy Manager (RETM) must assume responsibility for achieving sales objectives by implementing… more
- Genmab (NJ)
- …you and feel like a fit? Then we would love to have you join us! Manager , Statistical ProgrammingHands-on support of clinical trial reporting; Leading a team of ... compound level programming activities is in scope for this position.Responsibilities include: Review and input into key study level documents including CRF, SAP,… 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 ... for NN Deviation process within the PV domain, including review and disposition of submitted deviations in the Vault...of Quality Assurance for NN Change Control process, including review and disposition of submitted change requests in the… 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 ... for a living. Are you ready to make a difference? The Position The Manager PS Case Management is responsible for the management of receipt, documentation, triage 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 ... for a living. Are you ready to make a difference? The Position The Manager - Technical Complaints Call Center Oversight is responsible for overseeing the initial… more
- Genmab (NJ)
- …Operations functions as well as other organizations within Genmab, the Site Engagement Manager role will bring a high-touch and clinical trial 'face' with ... would love to have you join us!Overview:A Site Engagement Manager will support the vision and strategy of SE&F...clinical trial conduct and relationship quality through ongoing review , identification and resolution of issues and risks in… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …functionally with multiple functions and groups throughout the US organization, Clinical Development, Research & Early Development, other affiliates, and the Global ... lives of more patients than ever before. The Position The Brand Manager , Hemoglobinopathies is responsible for marketing activities directed at customer channels to… more
- Genmab (NJ)
- …The Senior Manager , Biostatistics acts as a biostatistician supporting the clinical development of compounds as compound lead, primarily up until proof of ... learningsRepresents Genmab during Key Opinion Leaders meetings Ensure biostatistician review of partner synopsis, protocols, statistical analysis plans, results… more
- Insmed Incorporated (NJ)
- …organization. The role will partner closely with Commercial and Clinical Supply Chain with responsibilities including supplier governance management, understanding ... sourcing projects in areas such as drug substance, drug product, clinical services, and packaging services within a contract manufacturing structureAbility to… more
- BioAgilytix (San Diego, CA)
- …you enable life-changing, life-saving therapeutics to the patients who need them.The Manager II will lead scientific and operational activities in support of ... preclinical, clinical , and product release studies for our San Diego...Identify new analytical techniques and technologies and lead their implementation. Review analytical instrument and equipment calibration, qualification and maintenance… more
- CoxHealth (Lake Spring, MO)
- Description :Job Summary ◦ The Clinical Documentation Integrity Educator will be responsible for working closely with the CDI Manager , CDI Supervisor, CDI Team ... throughout the CoxHealth System. Must be an expert in Clinical Documentation Integrity in order to analyze data to...CC/MCC captures. Will be responsible with working with CDI Manager and/or CDI Leadership designee to mentor/train new CDI… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …planning and execution of clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in ... 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
