- Merck & Co. (Boston, MA)
- …Atherosclerosis & Metabolism medicines span all phases of clinical development ( pre - clinical to post -licensure). The Senior Director will manage the ... reporting, and publication.Specifically, the Senior Director May Be Responsible For: Evaluating pre - clinical and translational work for the purpose of generating… more
- Merck & Co. (North Wales, PA)
- …Our company's Neuroscience Medicines span all phases of clinical development ( pre - clinical to post -licensure). With a focus on late-stage development, ... key opinion leaders. Specifically, the Senior Director May Be Responsible For: Evaluating pre - clinical and translational work for the purpose of generating early… more
- Merck & Co. (Rahway, NJ)
- …cardiovascular and respiratory medicines span all phases of clinical development ( pre - clinical to post -licensure). The Director will manage the entire ... analysis, regulatory reporting, and publication.Key Functions: Specific Responsibilities Evaluating pre - clinical and translational work for the purpose of… more
- Merck & Co. (Upper Gwynedd, PA)
- …Oncology medicines. Our Oncology medicines span all phases of clinical development ( pre - clinical to post -licensure). The Senior Director will manage the ... report to an Associate Vice President in the Oncology Clinical Research Group. Under the guidance of a supervisor,...the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees… more
- Memorial Healthcare System (Hollywood, FL)
- …your application to take advantage of this program. Employment is subject to post offer, pre -placement assessment, including drug testing. If you need reasonable ... a rewarding experience for our employees involved in their care. Summary: The Clinical Educator of Imaging Services has expert level knowledge in the respective… more
- Merck & Co. (North Wales, PA)
- …be expected to lead a Product Development Team (PDT) through late-phase clinical development and into post -licensure life-cycle management. This role demands ... Job DescriptionOur Clinical Research and Pharmacovigilance team pushes the boundaries...the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees… more
- Merck & Co. (Rahway, NJ)
- …support to the marketing groups for key molecules/products and clinical research expertise upon request.Conducts post -marketing studies.Prepares scientific ... Clinical Sciences, Clinical Site Management, Clinical Study Design, Clinical Trials Operations...the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …More Years post -law school experience in patent litigation, life sciences IP transactions work and/or patent prosecution required- 4 or More Years pharmaceutical ... is responsible for the protection of and maximization of Daiichi Sankyo's US IP portfolio and foreign counterparts. This position will handle all aspects of US… more
- Merck & Co. (North Wales, PA)
- …define, establish, and drive continuous improvement of the Business Process for the pre and post execution phases of Business Development Agreements with focus ... process and related activities associated with Global Regulatory Affairs and Clinical Safety (GRACS) Business Development Execution. The primary function includes… more
- Memorial Healthcare System (Hollywood, FL)
- …your application to take advantage of this program. Employment is subject to post offer, pre -placement assessment, including drug testing. If you need reasonable ... preliminary report of study data to Physician staff. Competencies: ACCOUNTABILITY, CLINICAL POLICIES AND STANDARDS, CUSTOMER SERVICE, IMAGE PRODUCTION, ANALYSIS AND… more
- Merck & Co. (Rahway, NJ)
- …of generating Real-World Evidence (RWE).Expertise in cohort identification using clinical and therapeutic classification codes such as ICD-9-CM, ICD-10-CM, SNOMED, ... including observational and retrospective designs.Working knowledge of research project operations , including contracting, procurement, and budget management processes.Strong interpersonal… more
- Merck & Co. (Rahway, NJ)
- … clinical trials to world-wide regulatory application submissions and post marketing support.The incumbent is responsible for the design and maintenance ... statistical programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and… more
- Merck & Co. (Biloxi, MS)
- …and USDA regulatory policies, dealing with bird health issues in customer's operations outside of vaccine related problems, customer complaints, and education of new ... bulletins.Assist in the design, execution, and analysis of field trials and clinical studies for new or existing products.Establish and maintain relationships with… more
- Merck & Co. (North Wales, PA)
- … clinical trials to world-wide regulatory application submissions and post marketing support.-The incumbent is responsible for the design and maintenance ... This position supports statistical programming activities for late stage drug/vaccine clinical development projects. This may include leadership of one or more… more
- Merck & Co. (Rahway, NJ)
- …the entire product lifecycle-from early development through commercialization and post -market activities-ensuring integration of HF principles to enhance patient ... and coach to the HF team and key stakeholders across R&D, clinical , regulatory, marketing, manufacturing, and quality functions.Educate and build awareness of HF… more
- Merck & Co. (North Wales, PA)
- …access and identifies value evidence needs to provide strategic input into clinical and market development programs.- Brings strong payer and HTA/reimbursement focus ... and market access needs in key global markets5+ years post PhD or 7+ years post Masters...the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees… more
- Merck & Co. (North Wales, PA)
- … clinical trials to world-wide regulatory application submissions and post marketing support.-Design and maintain statistical databases that support multiple ... statistical programming activities for multiple and/or large/complex late-stage drug/vaccine clinical development projects.Develop and execute statistical analysis and reporting… more
- Mountain View Pain Center LLC (Englewood, CO)
- …and restoring patient function and wellness. Position Summary: Assists in the daily clinical operations of the Preop/PACU in accordance with established federal, ... understanding of disease process and need for surgical intervention. Performs pre / post operative teaching to patient/significant other. Demonstrates appropriate… more
- Insmed Incorporated (NJ)
- …and manage regulatory submissions for compounds in various phases of clinical development, marketing applications, and post -approval lifecycle activities by ... abreast of all pertinent regulations and guidance documents for pre - and post -approval submissions. As needed, communicate...and conditions of each plan.Insmed Incorporated is an Equal Opportunity employer. We do not discriminate in hiring on… more
- Eisai, Inc (NJ)
- …training, at least four times a year, including scheduling and coordinating clinical touchpoints and workshops during the pre -work sessions, providing continuous ... to participants on their case study presentations and managing post -program follow-up and communication with graduates. Conduct supplemental training initiatives… more
