
11 - 50 employees
Founded 2016
đĽ Healthcare
đ§Ź Biotechnology
đ Pharmaceuticals
Healthcare ⢠Biotechnology ⢠Pharmaceuticals
Direct Biologics is a leader in the field of regenerative medicine, developing next-generation biologic products with a focus on Extracellular Vesicle (EV) products derived from adult human mesenchymal stem/stromal cells. These EV products offer clinical therapeutic potential and are a result of Direct Biologics' commitment to profound expertise in cellular and regenerative therapies. The company operates as a cGMP manufacturer, delivering cutting-edge clinical and scientific insights through extensive research. Direct Biologics is dedicated to revolutionizing the treatment of human diseases, leading the market with innovative regenerative biologic solutions.
đ September 23
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11 - 50 employees
Founded 2016
đĽ Healthcare
đ§Ź Biotechnology
đ Pharmaceuticals
Healthcare ⢠Biotechnology ⢠Pharmaceuticals
Direct Biologics is a leader in the field of regenerative medicine, developing next-generation biologic products with a focus on Extracellular Vesicle (EV) products derived from adult human mesenchymal stem/stromal cells. These EV products offer clinical therapeutic potential and are a result of Direct Biologics' commitment to profound expertise in cellular and regenerative therapies. The company operates as a cGMP manufacturer, delivering cutting-edge clinical and scientific insights through extensive research. Direct Biologics is dedicated to revolutionizing the treatment of human diseases, leading the market with innovative regenerative biologic solutions.
⢠Successful and timely execution of DM activities and deliverables in compliance with International Council for Harmonisation (ICH)/Good Clinical Practice (GCP) guidelines and Standard Operating Procedures (SOPs) ⢠Develops and/or approves DM documents, including Data Management Plans, Data Transfer Agreements, and Data Review Plans ⢠Designs and develops Electronic Data Capture (EDC) ⢠Oversees and coordinates EDC integrations ⢠Develops and maintains standard Case Report Form library ⢠Provides subject matter expertise to the development of trial documents, including Protocols, Monitoring Plans, Statistical Analysis Plans, and Clinical Study Reports ⢠Proactively identifies, mitigates, and manages risk in data management issues ⢠Develops and implements DM SOPs in partnership with Clinical Operations and Quality Assurance ⢠Manages DM external service providers (ESPs) ⢠Represents DM in interactions with regulatory authorities, as needed ⢠Applies current industry best practices to DM systems and processes ⢠Leads, trains and mentors DM personnel ⢠Performs other duties as assigned
⢠Strong knowledge of FDA regulations and ICH-GCP guidelines ⢠Thorough knowledge of the clinical research process ⢠Strong interpersonal skills with the ability to effectively communicate cross-functionally at all levels of the organization, as well as externally with stakeholders and ESPs ⢠Ability to identify issues and independently assess and recommend specific solutions ⢠Strong organizational skills, prioritization, time management, and cross functional collaboration ⢠BA/BS in life sciences relevant field, preferable ⢠10+ years of relevant industry experience ⢠Experience managing department personnel ⢠Experience with relevant EDC systems ⢠Proficiency in Microsoft Office 365
⢠Health Care Plan (Medical, Dental & Vision) ⢠Company 401k match up to 4% ⢠Paid Time Off (Vacation & Sick) ⢠Holidays ⢠Stock Option
Apply Nowđ September 23
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