
51 - 200 employees
🔧 Hardware
☁️ SaaS
IT Services • Hardware • SaaS
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.
🔥 0 minutes ago
🇺🇸 United States – Remote
💵 $20 - $24 / hour
⏰ Full Time
🟢 Junior
🧬 Research Scientist
🚫👨🎓 No degree required
🦅 H1B Visa Sponsor
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51 - 200 employees
🔧 Hardware
☁️ SaaS
IT Services • Hardware • SaaS
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 in support of the execution and management of projects and programs. • Based on business needs, may provide assistance to the following functional areas: Research Operations, Endpoint and Specialty Services, Site Operations, Data Management, Quality Control, Trial Master File. • Work closely with other team members to ensure timely completion of deliverables and resolution of issues. • Perform a variety of general administrative tasks such as filing, copying, and preparation of shipments for assigned projects. • Upload essential documents into eTMF system. • Perform quality control reviews of project-specific documentation and support submission of documents to the Trial Master File. • Perform ALCOA+ checks of documents uploaded into eTMF system. • Participate in project, program, functional area and general CPC meetings as required. • Assist in the preparation of Master Plans, Resource Materials, Source Documentation, Meeting Minutes, and submission of documents to the Trial Master File. • Coordinate and track receipt of project supplies to study sites. • Assist in tracking receipt, entry, upload, reviews and feedback to investigational sites of endpoint testing. • Assist in the development, administration, and tracking of 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.
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⏰ Full Time
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🦅 H1B Visa Sponsor
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