Clinical Data Manager

Responsibilities: Serve as lead CDM on assigned clinical trials by attending internal and external clinical trial project team meetings. Responsible for the study–specific data management tasks from protocol review to database lock to ensure data are collected, reviewed, and delivered with high quality, on–time, and within scope. Responsible for...

Professional Summary: Under limited supervision, works collaboratively with vendor Project Managers and Clinical Data Managers to assure that Data Management functions are performed in compliance with regulations and according to study protocol and Study Data Management Manual (DMM). Works with involved parties to assure that DMM is prepared according to...

Responsibilities: Project level coordination of and day to day oversight of DM tasks including Review all DM documents within a project area to ensure a consistent approach and review of project timelines and metrics to ensure databases are delivered to set timelines and approve database locks and unlocks. Ensure that quality control checks are occurring...

Roles & Responsibilities: Work with DB programmers to design (e)CRFs and edit checks in EDC system for complex studies Lead, coordinate, and perform User Acceptance Testing (UAT) tasks for complex studies and modules Ensure proper completion of QC and UAT of EDC tools and modules, including database testing, data export testing, and testing of custom...

Roles & Responsibilities:Work with DB programmers to design (e)CRFs and edit checks in EDC system for complex studies Lead, coordinate, and perform User Acceptance Testing (UAT) tasks for complex studies and modules Ensure proper completion of QC and UAT of EDC tools and modules, including database testing, data export testing, and testing of custom...

Responsibilities: Lead data management activities as a program–level lead data manager in support of Alnylam clinical studies. Lead database build activities including leading cross–functional review of eCRF content, review of edit check specifications, and perform user acceptance testing. Monitor data collection, coding, and cleaning by vendors...

Responsibilities: Lead data management activities as a program-level lead data manager in support of Alnylam clinical studies. Lead database build activities including leading cross-functional review of eCRF content, review of edit check specifications, and perform user acceptance testing. Monitor data collection, coding, and cleaning...

Responsibilities: Oversee data management activities for multiple clinical studies. Ensure data quality and integrity from study start–up through database lock. Develop and implement data management plans, including data validation and quality control procedures. Design and review case report forms (CRFs) and electronic CRFs (eCRFs) for data...

Responsibilities: Oversee data management activities for multiple clinical studies. Ensure data quality and integrity from study start-up through database lock. Develop and implement data management plans, including data validation and quality control procedures. Design and review case report forms (CRFs) and electronic CRFs (eCRFs) for...

About the Job:You will critically review DM documents for accuracy and acceptability for junior level CDMs to ensure standards for data collection are applied to all studies.You will train and supervise clinical data associates.You will collaborate with all cross-function team members including Clinical Operations, Biostatistics, Statistical Programmers,...

Responsibilities: Works collaboratively with Clinical Development staff to meet project deliverables and timelines for statistical data analysis and reporting. Assesses the quality and consistency of analysis data and performs cross–study analyses. Uses internal macros or writes SAS macros to automate study deliverables. Works as a primary...

Company DescriptionAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in...

Responsibilities: Site Management experience (site or sponsor). Knowledge of/experience with CTMS/EDC/TMF. Experience with Good Clinical Practice (GCP). Oversees, designs, plans, and develops clinical evaluation research studies. Prepares and authors protocols and patient record forms. Conducts registered and nonregistered clinical studies of...

Job DescriptionJob DescriptionPOSITION SUMMARY: Manager/Sr. Manager serves as an functional lead for clinical data management who will lead cross-functional team members to perform all data management activities to ensure data quality, integrity, and compliance with health authority guidelines and standard. This role will report to the Head of Biometrics....

Job DescriptionJob DescriptionSalary: Alumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer - our goal is to fundamentally change the outcomes for these patients. The...

Alumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer - our goal is to fundamentally change the outcomes for these patients.   The Associate Director, Data Management...

Role: SAP Data MigrationLocation: Plainfield, NJFulltime - OnsiteResponsibilities:Lead SAP data migration projects with a minimum of 5 years of relevant experience.Demonstrate strong knowledge of SAP modules such as FI/CO, MM, SD, PP, and others.Utilize SAP data migration tools like LSMW, BODS, SAP Data Services, and more.Perform data analysis,...

Role: SAP Data MigrationLocation: Plainfield, NJFulltime - OnsiteResponsibilities:Lead SAP data migration projects with a minimum of 5 years of relevant experience.Demonstrate strong knowledge of SAP modules such as FI/CO, MM, SD, PP, and others.Utilize SAP data migration tools like LSMW, BODS, SAP Data Services, and more.Perform data analysis,...

The Position We advance science so that we all have more time with the people we love The mission of the Data Intelligence team in the Early Clinical Development (ECD) department at Genentech is to optimize the support of clinical systems to provide high-quality clinical trial data insights and to offer data science-related consultation to the study teams....

Job DescriptionJob DescriptionORGANIZATIONRemeGen Biosciences is a biopharmaceutical company, focusing on the discovery and development of innovative medicines for the treatment of cancer and autoimmune diseases, based in South San Francisco, California, and Rockville, Maryland. By leveraging our deep insights into oncology and immunology, advanced protein...