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Research Assistant

Company: Tilda Research
Location: Birmingham
Posted on: August 5, 2022

Job Description:

Why work at Tilda?Our mission is to accelerate clinical innovation. As a tech-enabled clinical trial network, we build software and services to help pharma innovators better execute their clinical trial programs. Our work leads to faster cures and thus institute a meaningful impact on millions of lives. You can help us realize that goal.Work with some of the best researchers in the world: Our team of physicians and researchers are passion-driven, and have a long history of accomplishments. They have worked on hundreds of research studies, helping bring many new medical innovations to the market.Join us at a magical time: We've hit revenue growth and product-market fit, which gives us a huge green field to work with. You'd join at the perfect time to shape what we build and how we grow. We are a Silicon Valley-based company, backed by leading venture capital and healthcare investors.Purpose of Position:Serve as liaison between Tilda Staff and the Site Principal Investigator(s), and Sub-Investigator(s).Responsibilities:1. Site preparation and ensuring site quality2. Assisting with completing study visits3. Maintaining and dispensing study product and supplies, through appropriate oversight by Clinical Research Coordinators (CRC) and Site Manager.4. Completing and ensuring the quality of case report forms, electronic data capture (EDC) forms and information into the clinical trials management system (CTMS)5. Processing and preparing laboratory specimens for shipment6. Performing electrocardiograms (ECG) in the presence of Clinical Research Coordinators and study aligned clinicians7. Ordering supplies from study aligned vendors8. Inventory tracking in collaboration with on-site Clinical Research Coordinators (CRC)9. Shipping supplies and labs to study aligned vendors.10. Maintaining source documents (e.g. through digitization or completion of eSource in clinical trial management system).11. Responding to queries in a timely manner (e.g. a liaison between the CRC and data entry team).12. Filing of study-related documentation in CTMS and/or electronic Trial Master File.Education/Skill/Experience Requirements:Impeccable attention to detail and appreciates organized workflowsOne to three years of experience in a clinical setting.Familiarity with ICH/GCP principlesExperience/Training:Phlebotomy and ECG experience preferred;Bloodborne Pathogen and IATA Certification (shipping of dangerous goods) will be provided.Proficiency with technology (G-Suite).Definitions:CTMS - Clinical Trial Management System (CRIO)eTMF - Electronic Trial Master File - SiteVaultFor more information about Tilda Research, please visit https://tilda.bio/A bit of info about who we are: We are a Bio-IT startup based in San Francisco, backed by two of the largest health care institutional investors: 8vc (https://8vc.com/bio-it) and Optum / United Health Group (Fortune #5 company). We are an innovator in clinical research execution and work with some of the largest pharma companies to accelerate their medical innovations to market. We are currently in stealth mode and have a limited web presence. We are scaling Series A startup. Our founders are successful serial entrepreneurs, with three of their past companies leading to IPOs (VMware, MobileIron) or exits (LexentBio acquired by Roche).

Keywords: Tilda Research, Birmingham , Research Assistant, Other , Birmingham, Alabama

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