Clinical data management (CDM) is a critical process in clinical research, which leads to generation of high-quality, reliable, and statistically sound data from clinical trials. Clinical data management ensures collection, integration and availability of data at appropriate quality and cost. It also supports the conduct, management and analysis of studies across the spectrum of clinical research as defined by the National Institutes of Health (NIH). The ultimate goal of CDM is to ensure that conclusions drawn from research are well supported by the data. Achieving this goal protects public he ...
alth and confidence in marketed therapeutics.
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Veeva [NYSE: VEEV] is the leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, our customers range from the world’s largest pharmaceutical companies to emerging biotechs. Veeva’s software helps our customers bring medicines and therapies to patients faster. We are the first public company to become a Public Benefit Corporation. As a PBC, we are committed to making...
JOB SUMMARY. Responsible for leading, planning and execution of all data management activities for assigned projects, ensuring focus on data integrity, validity, reliability in accordance with standard processes, sponsor guidelines, industry best practices and regulatory standards. Act as coach, mentor and/or Subject Matter Expert within the department, aiding Manager in process improvements, issue escalation and training development and deliver...
Company DescriptionCrowd StaffingJob DescriptionMinimum QualificationsSkills:Experience with Electronic Data Capture (EDC)Excellent verbal and written communication skills and strong interpersonal skillsExperience managing Clinical Research Organizations (CROs)Familiarity with clinical data management systemsSAS programming experience a plusAnalytical and Communication skillsPlanning and Co-ordination skillsExperience with project managementExper...
JOB SUMMARY. Responsible for leading, planning and execution of all data management activities for assigned projects, ensuring focus on data integrity, validity, reliability in accordance with standard processes, sponsor guidelines, industry best practices and regulatory standards. Act as coach, mentor and/or Subject Matter Expert within the department, aiding Manager in process improvements, issue escalation and training development and deliver...
Ocular Therapeutix, Inc. (NASDAQ:OCUL) is a biopharmaceutical company focused on the formulation, development, and commercialization of innovative therapies for diseases and conditions of the eye using its proprietary bioresorbable hydrogel-based formulation technology. Our robust product pipeline positions Ocular Therapeutix to become a leader in the ophthalmic space due to our ability to create drug delivery solutions that reduce the complexity...
Company DescriptionMindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at http://www.mindlance.com. Job DescriptionTitle: Clinical Data ManagerLocation: Woodcliff Lake, NJDuration: 1 year (Extendable contract)Responsibilities• Independently performs all data management functions to ensure timely and quality database lock for studies Phase I-III. Perform data...
About BridgeBio. BridgeBio. is a biopharmaceutical company founded to discover, create, test, and deliver transformative medicines to treat patients who suffer from genetic diseases and cancers with clear genetic drivers. We bridge the gap between remarkable advancements in genetic science in academic institutions and the delivery of meaningful medicines to patients. Founded in 2015, the company has built a portfolio of 20 drug development progra...
Job Summary. The Clinical Data Scientist works with the data science team to collect clinical data for machine learning algorithm development, for clinical studies related to FDA submission, and for research and scientific communications purposes. Responsibilities involve working with clinical data scientists to conduct clinical studies, analyzing data, managing IRB-related regulatory documentation, and acting as a bridge between DeepHealth and e...
Why Join Intellia. Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases. Beyond our science, we live our four core values: One, Explore, Disrupt, Deliver and feel strongly that you can achieve more at Intellia. We have a single-minded determination to excel and succeed together. We believe in the power of curiosity and pushing boundaries. We...
HOW MIGHT YOU DEFY IMAGINATION. If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be prou...
Position Summary. . Responsible for conceptualizing, organizing, and overseeing data management activities for the Clinical Affairs department. Manage Clinical Data Specialists to ensure all aspects of study data collection, management, and analysis meet the requirements to support regulatory submission of bioMérieux's molecular. in vitro. diagnostic products or other research activities. Make significant contributions to the generation of docume...
Description. Position Summary. Responsible for conceptualizing, organizing, and overseeing data management activities for the Clinical Affairs department. Manage Clinical Data Specialists to ensure all aspects of study data collection, management, and analysis meet the requirements to support regulatory submission of bioMrieux's molecular. in vitro. diagnostic products or other research activities. Make significant contributions to the generation...
