- Aequor (Thousand Oaks, CA)
- …leadership and accountability. Core Competencies: Technical Expertise: o Deep knowledge of clinical data management processes and systems (eg, EDC, CDISC ... & Knowledge Minimum of 10 years of experience in clinical data management or related field. Proven...OR Bachelor's degree and 6 years of experience OR Associate 's degree and 10 years of experience OR High… more
- Eisai, Inc (Phoenix, AZ)
- …If this is your profile, we want to hear from you. The Senior Oncology Sales Specialist is responsible for meeting/exceeding sales goals through promoting Oncology ... products within an assigned territory in a compliant and appropriate manner. The Senior Oncology Sales Specialist represents and promotes assigned brand(s) in the IV… more
- Merck & Co. (Rahway, NJ)
- …effectively communicate with stakeholders at various levels, including cross-functional teams, senior management, external vendors, and clinical sites. Strong ... Business, Business Risks, Change Management, Clinical Development, Clinical Research, Cross-Functional Team Leadership, Data Analysis, Detail-Oriented,… more
- Eisai, Inc (Nutley, NJ)
- … Clinical Programming manages and oversees JReview and SAS program development for clinical data processing, data review reports and listings. This ... your profile, we want to hear from you. The Associate Director, Clinical Programming must have expertise...programming support & upgrades Manage automated process for converting clinical data to standard normalized datasets which… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to ensure appropriate biomarker, PK / PD measurements; Reviews emerging clinical data regularly; Leads dose-escalation meetings; Performs quality assessment ... trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs.… more
- Genmab (NJ)
- …to have you join us!The Global Regulatory Labeling, Policy and Intelligence Associate Director will primarily be responsible for leading the development and ... maintenance of global labeling documents (eg, Core Data Sheet, USPI, EU SmPC and related patient information)...Global Regulatory Affairs (GRA) and will report to the Sr . Director, Labeling, Policy and Intelligence. The position may… more
- Merck & Co. (North Wales, PA)
- …Biopharmaceutics, Clinical Reporting, Clinical Testing, Clinical Trials Analysis, Communication, Data Management, Epidemiology, Health ... research support for Oncology programs.- The position reports to the Senior Director responsible for Portfolio Real-world Evidence (RWE) in Oncology.- -Position… more
- Merck & Co. (Rahway, NJ)
- …Care Pharmacy (AMCP) dossiers for US payers, and Global Value DossiersDevelops supplementary clinical data package in close partnership with markets and HTA ... Job DescriptionRole SummaryUnder the guidance of a senior leader, an Associate Principal Scientist/ Associate Director, has primary responsibility for… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …strategy, focusing on every touchpoint that impacts our customers. We leverage data and insights to inform our decision-making processes, ensuring that our ... design pull you in? Are you ready to experiment with us? The Position The Associate Director of Nephrology Key Opinion Leader Marketing will be a pivotal driver in… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …implementation of a CDx study/IVDR performance evaluation study integration of an assay into clinical testing (before testing) and once data is ready for CDx ... between CTA/CDx assays, prospective vs retrospective analyses and collection, missing data , demographic/representativeness of samples from clinical trial and… more
- Daiichi Sankyo, Inc. (New Orleans, LA)
- …research, academic or US-managed markets preferredPrevious experience in Oncology, clinical research and medical education preferredPrincipal MSL/ Associate ... the following: Presenting disease state and Daiichi Sankyo product specific data to HCPsResponding to unsolicited requests for medical informationIdentifying and… more
- Merck & Co. (North Wales, PA)
- …with senior cross-functional leadership to optimize efficiencies in the clinical development space. Preferred skills include experience in the application of AI, ... and vaccines for the benefit of patients and global human health.The Associate Vice President (AVP), Late Development Statistics, BARDS, is responsible and… more
- Merck & Co. (Rahway, NJ)
- …of Biologics and Biopharmaceutics, have 10-15 direct reports composed of experienced, senior and associate scientists.- The successful candidate will effectively ... opportunity is fast paced and contributes to the Pharmaceutical Sciences and Clinical Supplies (PSCS) deliverable which is the development of robust compositions,… more
- Antech Diagnostics (Great Neck, NY)
- …to strategic insights. While this role operates independently within the Operations function, the Senior Data Analyst will work closely with corporate data ... job-related skills, experience, education, training and budget. Job Purpose/Overview: The Sr . Operations Data Analyst is responsible for providing actionable… more
- The University of Miami (Miami, FL)
- …University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time Sr . Research Associate 3 to work at the UHealth Medical Campus in ... Miami, FL. CORE SUMMARY The Sr . Research Associate 3 conducts highly specialized...major goal of our lab is to generate preclinical data for clinical translation. Relevant experience in… more
- Boehringer Ingelheim Pharmaceuticals, Inc (Ridgefield, CT)
- …benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Senior Associate Director, Medical Customer Facing Excellence (MCFE) will ... and teams, MSLs, AMAs, Medicine Excellence, Global Medical Affairs, Clinical Operations, HP Ops, Comm Ops, Legal and Compliance....Must be 18 years of age or older. Compensation Data : This position offers a base salary typically between… more
- Adventist Health (Roseville, CA)
- …Compliance Program. Job Requirements: Education and Work Experience: Associate 's/Technical Degree or equivalent combination of education/related experience: Required ... (CEMA) or Certified Documentation Integrity Practitioner (CDIP) or Certified Clinical Documentation Specialist- (CCDS) or CIRCC-AAPC or Radiation Oncology Certified… more
- Invivyd (New Haven, CT)
- …Be part of making a difference. Be part of Invivyd. Job Title: Senior Manager/ Associate Director, Drug Safety and Pharmacovigilance Operations Position summary: ... The Sr . Manager/ Associate , Drug Safety and Pharmacovigilance Operations...tracking, storing, and reporting of serious adverse events from clinical trials , Provide direct technical / data … more
- Bristol-Myers Squibb Company (Princeton, NJ)
- …and validation partnering with Translational Sciences colleagues when applicable Manages clinical biomarker data delivery and analysis and associated timelines ... of the Global Research organization in BMS and leads late stage clinical , pharmacological and translational research and development activities for the pipeline and… more
- Children's National Hospital (Washington, DC)
- The Senior Program Associate will work closely with directors and managers in the Programs and Research department to align program activities with the Safe Kids ... the following injury areas: Road, Home and/or Play. The Senior Program Associate will serve as a...and effectively to internal and external audiences, analyze program data and coordinate reporting. Domestic travel may be required.… more
