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8 associate director clinician medical monitor vaccines jobs found

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associate director clinician medical monitor vaccines
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TB
Full Time
 
Associate Director, Clinician Medical Monitor, Vaccines
Taleo BE Pearl River, NY, USA
ROLE SUMMARY: The Clinician Medical Monitor (CMM) is accountable for providing medical and scientific expertise and oversight for Global Clinical Trials and serves as a single point of accountability for design, execution, monitoring, delivery and reporting of one or more clinical studies to ensure patient safety. Additional study level activities include presentation of study results to internal and external committees or advisory boards, presentation of data at international scientific meetings and publication of study results in peer reviewed journals. The CMM will also act as a medical monitor for select clinical trials, including phase 2B and phase 3 registration studies, The CMM is accountable for patient safety for subjects participating in Pfizer clinical trials and provides medical guidance during the design, execution, and reporting for clinical studies. In addition to study level activities, the CMM will participate in program level activities including...

Sep 22, 2023
Wo
Full Time
 
Associate Director, Clinician Medical Monitor, Vaccines
Workday Pearl River, NY, USA
ROLE SUMMARY The clinician medical monitor may contribute towards providing medical and scientific expertise and oversight for Clinical Trials. The clinician medical monitor may be required to design a development strategy for multiple protocols designed to obtain worldwide approval for a compound or group of compounds. The clinician will work also collaboratively with members of clinical development teams across studies and across the Pfizer enterprise on digital health technologies and digital endpoint development ROLE RESPONSIBILITIES Develop plans for implementation, validation, and/or qualification of digital health technologies into clinical development programs and clinical trials Accountable for the design of protocols, clinical reports, clinical portions of regulatory submissions, protocol amendments and conducts data review, analysis, and interpretation of data from studies. Accountable for safety across the study: Provide study team with...

Sep 22, 2023
TB
Full Time
 
Associate Director, Clinician, Medical Monitor, Vaccines
Taleo BE Pearl River, NY, USA
ROLE SUMMARY The clinician medical monitor is a member of an energetic team working on an innovative RSV candidate vaccine and is accountable for providing medical and scientific expertise and oversight for Clinical Trials and serves as a single point of accountability for design, execution, monitoring, delivery and reporting of one or more clinical studies and to ensure patient safety. In addition to study level activities, the clinician medical monitor will participate in standing committees, review compounds for potential in-licensing, including performance of due diligence reviews, and provide assistance to new business development on market opportunities and the target product profile. ROLE RESPONSIBILITIES   Accountable for safety across the study: Provide study team with medical advice for all medical issues during risk assessment and mitigation planning to enable quality, compliance and patient safety at the trial, site and patient level. Ensures...

Sep 15, 2023
Wo
Full Time
 
Associate Director, Medical Monitor, Vaccines
Workday Collegeville, PA, USA
ROLE SUMMARY The clinician medical monitor may contribute towards providing medical and scientific expertise and oversight for Clinical Trials of pneumococcal vaccines or other vaccine programs. The clinician medical monitor may be required to design a development strategy for multiple protocols designed to obtain worldwide approval for a compound or group of compounds. ROLE RESPONSIBILITIES Accountable for safety across the study: Provide study team with medical advice for all medical issues during risk assessment and mitigation planning to enable quality, compliance and patient safety at the trial, site and patient level. Ensures development of and adherence to the Safety Surveillance Review Plan (SSRP).Consistent with the SSRP, performs and documents regular review of individual subject safety data, and performs review of cumulative safety data with the safety risk lead. As appropriate, the clinician medical monitor may delegate these responsibilities...

Sep 18, 2023
EU
Associate Director, Medical Science Liaisons, Alzheimer's Disease and Brain Health
Eisai US Bridgeport, CT, USA
Associate Director, Medical Science Liaisons, Alzheimer's Disease and Brain Health page is loaded Associate Director, Medical Science Liaisons, Alzheimer's Disease and Brain Health Apply remote type Field Based locations United States, Field Based Connecticut, Bridgeport Massachusetts, Boston Pennsylvania, Pittsburgh New Jersey, Newark time type Full time posted on Posted 16 Days Ago job requisition id R3016 At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai’s human health care (hhc) mission. We’re a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer’s disease. As we continue to expand, we are...

Sep 22, 2023
MC
Medical Assistant Supervisor - Farmington
Minnesota Community Care Farmington, MN, USA
Job Details Level Experienced Job Location Farmington - Farmington, MN Position Type 1.0 FTE Education Level Associates Degree Salary Range $56,000.00 - $63,000.00 Salary Travel Percentage Negligible Job Shift Clinic Hours Job Category Healthcare Descriptions The MA supervisor position supports the Clinic Manager in the care of patients in a culturally diverse population within a clinic setting. The position is responsible for providing clinical oversight and leadership for all Medical Assistant (MA) staff, maintaining the quality and adequacy of MA practice. Essential Functions Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Responsible for the recruitment, hiring, supervision, development, competency assessment and performance evaluation of MA staff Reviews and approves timecards and coordinates time off requests for MA staff Assists with completion of weekly clinic schedule as...

Sep 22, 2023
Sa
Associate Director Medical Value & Outcomes
Sanofi Albany, NY, USA
Associate Director, Medical Value & Outcomes Job Summary The Medical Value & Outcomes team member (Senior Manager, Associate Director or Director) serves as the medical scientific lead for population-based healthcare decision makers to facilitate scientific exchange on disease state management and the value of Sanofi products, to provide insights to internal teams on key evidence gaps relevant to healthcare decision-makers, and to identify/facilitate research, education, and other collaborations per applicable SOPs. This position represents the MS and Immunology franchises serving as the MVO lead for assigned strategic regional accounts. The position supports the strategic and cross functional alignment within the organization in order to achieve the medical mission of safe and appropriate use of Sanofi therapies. The MVO assists in the development of Integrated Medical Plans through collaboration with Medical Communications and Publications, Medical Science Liaisons,...

Sep 22, 2023
TB
Full Time
 
Associate Director, Medical Monitor
Taleo BE Pearl River, NY, USA
Associate Director, Clinician, Medical Monitor ROLE SUMMARY The Clinician Medical Monitor (CMM) is accountable for providing medical and scientific expertise and oversight for Global Clinical Trials and serves as a single point of accountability for design, execution, monitoring, delivery and reporting of one or more clinical studies to ensure patient safety. Additional study level activities include presentation of study results to internal and external committees or advisory boards, presentation of data at international scientific meetings and publication of study results in peer reviewed journals. The CMM will also act as a medical monitor for select clinical trials, including phase 2B and phase 3 registration studies, The CMM is accountable for patient safety for subjects participating in Pfizer clinical trials and provides medical guidance during the design, execution, and reporting for clinical studies. In addition to study level activities, the CMM will...

Sep 18, 2023
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