- Novo Nordisk Inc. (WA)
- …clinical trials and improvement/innovation projects for NACD and Novo Nordisk (eg, clinical trial site staff, clinical research vendors). Manages ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...scientific integrity; regulatory and process compliance) for monitoring and site management activities. Takes ownership to deliver upon near-term… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …collaborates with lead statistician on SAP update, as needed. Provides input to Clinical Operations on site issues. Contributes to development of CSR.External ... immune disorders. Summary Drafts development plans, protocol profile, protocol, and clinical sections of submission documents under guidance of CSL and/or Medical… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and deliver training programs for internal teams ( Clinical Development, Clinical Operations, etc.), investigators, and site staff to enhance awareness ... around rare diseases and immune disorders.Summary The Head of Clinical Trial (CT) Diversity sits within Global Oncology ...trial diversity plans Leads the strategy of country and site selection across assets from the perspective of accomplishing… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …on the project level Act as a liaison between the company and clinical site investigators and KOLs Interface together with VP Medical/Scientific Development ... MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating a distinct R&D… more
- Merck & Co. (Rahway, NJ)
- …a deep understanding of clinical trial design and operations, clinical research site management, patient enrollment and retentionProven experience working ... diverse enrollment.The Diversity Program Lead will align with the clinical trial team to define diversity enrollment goals and...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …activities in collaboration with the CRO and the study team. Oversee the site qualification process.Monitor clinical trial performance and quality metrics and ... will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions, in...a timely manner and with quality (eg communication plan, site monitoring plan, etc.) as per study plan.Responsible for… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …activities in collaboration with the CRO and the study team. Oversee the site qualification process.Monitor clinical trial performance and quality metrics and ... and immune disorders.SummaryThe incumbent will be responsible for ensuring execution of clinical studies across geographic regions, in adherence to Good Clinical … more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …or gaps at the manufacturing sites.- Conduct scouting activities and recommend CDMOs for clinical and launch site selection from Tech Mgmt. (mAb, Drug Substance, ... Sankyo, until completion of the first CPV. The candidate is leading the Site Launch Team with its associated sub-teams. Accordingly, the candidate is responsible for… more
- The University of Vermont Health Network (Burlington, VT)
- …service in the same department.This position assists with the daily activities of a clinical site and facilitates the flow of patients by providing clerical and ... clinical health care support to patients and family under...of a provider. The position requires mastery of basic clinical activities and some advanced clinical activities.EDUCATION:High… more
- Taiho Oncology (TX)
- …with Taiho sponsored trials as assigned, which may include providing recommendations for site selection, clinical data presentation at site initiation or ... on Taiho products and relevant disease states, and facilitation of clinical research. The MSL integrates clinical /scientific expertise and knowledge… more
- Taiho Oncology (New York, NY)
- …with Taiho sponsored trials as assigned, which may include providing recommendations for site selection, clinical data presentation at site initiation or ... and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources… more
- Merck & Co. (North Wales, PA)
- …study sites and identifies potential investigators to participate in phase II-IV clinical development programs, conducts Site Initiation Visits (SIVs), and ... policiesMaintains current knowledge and comprehension of dynamic scientific and clinical environment in the Company's Areas of Interest (AOI)ResearchUpon request… more
- Merck & Co. (North Wales, PA)
- …of study start up by reducing the time from study initiation to first site ready.Remove obstacles and enable the Global Clinical Trial Organization to focus ... accurate data collected from patients who are part of Clinical Trials. Trial Standards, Trial Design, Trial Data Collections,...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Respiratory will focus on driving strategy, development, and life-cycle ... organization therefore requiring someone who has built and lead clinical development plans from the ground up. They will...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders.SummarySenior clinical operational leader accountable for operational planning and execution of ... FIH, clin pharm patient studies, and Phases 1-3 clinical trials at the study and program level. Responsible...plan agreed to by the Global Project Team (GPT).Lead site selection and site qualification discussions, kick-off… more
- Merck & Co. (North Wales, PA)
- …Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our company's ... Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionIt is critical that, for all company-sponsored clinical trials, patient safety, high quality data and compliance with company requirements and ... Sr CCQM Lead supports large to medium size country/cluster clinical trial operations to achieve those objectives. -Under the...performs QC activities (incl. QCVs) and conducts ad hoc site visits upon request.-On a regular basis and in… more
- Merck & Co. (North Wales, PA)
- …Summary: This position leads the scientific planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have the ... cross-functional team.Job Responsibilities: Responsible for leading specific aspects of clinical /scientific execution of clinical protocol(s). This may… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPrimary activities include, but are not limited to:Responsible for clinical database design and development activities supporting startup of a ... clinical trial.Activities supported may include standards technical component development...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… 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 the West, in ... adherence to Good Clinical Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food...overall study plan provided by the CRO. Participate in site selection and site qualification with (study… more
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