
51 - 200 employees
🏥 Healthcare
📦 Logistics
💼 Consulting
Healthcare • Logistics • Consulting
CPC is a trusted tech partner that specializes in IT support and IT services, providing a wide range of solutions including sales and maintenance of new, used, and factory recertified computer hardware and software. Established in 1962, CPC leverages a deep bench of engineers and consultants to offer innovative and efficient IT solutions tailored to both businesses with or without internal IT departments. With a focus on value, innovation, reputation, and excellence, CPC supports various industries including remote work, healthcare, and manufacturing, ensuring businesses stay up, running, and protected. The company partners with leading tech brands such as Citrix, IGEL, LG, Nutanix, Arctic Wolf, NoMachine, Zebra Technologies, and DELL, and offers both new and refurbished equipment. CPC is committed to enhancing business operations through effective IT solutions and services.
🕒 3 days ago
⛰️ Colorado – Remote
💵 $20 - $24 / hour
⏰ Full Time
🟢 Junior
🧬 Research Scientist
🚫👨🎓 No degree required
🦅 H1B Visa Sponsor
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51 - 200 employees
🏥 Healthcare
📦 Logistics
💼 Consulting
Healthcare • Logistics • Consulting
CPC is a trusted tech partner that specializes in IT support and IT services, providing a wide range of solutions including sales and maintenance of new, used, and factory recertified computer hardware and software. Established in 1962, CPC leverages a deep bench of engineers and consultants to offer innovative and efficient IT solutions tailored to both businesses with or without internal IT departments. With a focus on value, innovation, reputation, and excellence, CPC supports various industries including remote work, healthcare, and manufacturing, ensuring businesses stay up, running, and protected. The company partners with leading tech brands such as Citrix, IGEL, LG, Nutanix, Arctic Wolf, NoMachine, Zebra Technologies, and DELL, and offers both new and refurbished equipment. CPC is committed to enhancing business operations through effective IT solutions and services.
• Serve as a floating resource to perform a variety of activities supporting the execution and management of projects and programs • Provide assistance to Research Operations, Endpoint and Specialty Services, Site Operations, Data Management, Quality Control, and Trial Master File based on business needs • Work closely with team members to ensure timely completion of deliverables and resolution of issues • Perform general administrative tasks including filing, copying, and preparing shipments for assigned projects • Upload essential documents into the eTMF system • Perform quality control reviews and support submission of project-specific documentation to the Trial Master File • Perform ALCOA+ checks of documents uploaded into the eTMF system • Participate in project, program, functional area, and general CPC meetings as required • Assist with preparation of Master Plans, Resource Materials, Source Documentation, Meeting Minutes, and Trial Master File submissions • Coordinate and track receipt of project supplies to study sites • Track receipt, entry, upload, reviews, and feedback to investigational sites of endpoint testing • Assist in developing, administering, and tracking project-specific training • Manage email reconciliation and export at study close-out • Collect and review investigational site documentation and process as directed • Correspond with investigational sites, CPC staff, and sponsors to rectify data queries and collect outstanding documentation • Serve as one of the primary points of contact for investigational sites • Perform query management, report generation, and data reconciliation tasks • Assist with User Acceptance Testing (UAT) • Manage user access requests, including user reconciliation • Perform general data review of study data in EDCs
• GED or HS Diploma required • Nursing or bachelor’s degree preferred • Minimum of 1 years of experience working in a clinical research (or similar) setting • Higher degree may be considered in lieu of experience • Demonstrated ability to complete core tasks with minimal direction, while reliably escalating for guidance on less routine assignments • Thorough knowledge of the Good Clinical Practice guidelines and the applicable FDA and ICH regulations for conducting clinical drug trials • Good understanding of the drug development process • Proficiency in MS Office, particularly spreadsheet databases and word-processing • Excellent communication and organizational skills • Great attention to detail • Ability to work with others in a manner that promotes group effort and achievement • Ability to shift priorities quickly while ensuring accuracy and timely completion of tasks • Ability to manage conflicts and resolve problems effectively • Ability to discern priorities and obtain direction to accomplish day-to-day tasks
• Comprehensive benefits package (medical, dental, vision, life, STD, LTD etc.) • Matching 401(k) plan (dollar for dollar up to 4% of your eligible compensation, fully vested immediately) • 11 paid holidays • 15 - 25 vacation days based on years of service • Paid sick time (2.67 hours accrued bi-weekly up to a maximum of 80 hours) • Flexible and remote work schedules
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