CPC yra IT palaikymo ir paslaugų įmonė, padedanti organizacijoms palaikyti patikimas ir saugias technologijų aplinkas. 1962 m. įkurta įmonė derina inžinerijos ir konsultavimo kompetenciją su naujos, naudotos ir gamykloje atnaujintos kompiuterinės techninės bei programinės įrangos pardavimu, priežiūra ir palaikymu. Jos sprendimai skirti įmonėms, turinčioms vidines IT komandas arba veikiančioms be jų, sveikatos priežiūros, logistikos, konsultavimo, nuotolinio darbo ir gamybos srityse. CPC bendradarbiauja su tokiais technologijų tiekėjais kaip „Citrix“, „IGEL“, „LG“, „Nutanix“, „Arctic Wolf“, „NoMachine“, „Zebra Technologies“ ir „Dell“, teikdama klientams praktiškus infrastruktūros ir darbo vietų technologijų sprendimus. Įmonės samdos kontekstas atspindi į paslaugas orientuotą komandą, kurios tikslas – užtikrinti efektyvią IT veiklą ir patikimą techninę pagalbą.
CPC Clinical Research Intern Hybrid
Support CPC’s academic clinical trial design and management programs through regulatory submissions, Trial Master File quality checks, clinical operations meetings, and study-site activities.
Aprašymas
- Create presentation slides covering academic activities for monthly staff meetings
- Support monthly scientific Lunch & Learns by helping select speakers, prepare slides, order meals, and set up and clean conference rooms
- Join clinical trial operations calls and document meeting minutes
- Take part in clinic shadowing with physician faculty
- Complete Trial Master File submissions and quality reviews while developing TMF knowledge
- Support regulatory filings and public trial registry updates for sponsored studies
- Help collect site regulatory documents during study start-up shadowing
- Develop familiarity with Clinical Trial Management System functions
- Complete Institutional Review Board submissions
- Learn budget processes and finance-team responsibilities
- Attend Site Endpoint Evaluation Visits and remote training on functional endpoints
- Observe medical monitoring, narrative writing and shell development, DSMB, adjudication, and committee management activities
- Conduct research using ClinicalTrials.gov and PubMed
Reikalavimai
- Currently enrolled in an undergraduate or graduate scientific degree program
- Available to attend in-person training
- Strong communication and organizational abilities
- Careful, detail-oriented approach with sound critical-thinking skills
- Proficient in Microsoft Word, PowerPoint, and Excel
- Available for occasional office visits
- Able to successfully complete background and education verification
Privalumai
- Flexible scheduling of 10–40 hours per week to accommodate school commitments
- Opportunities for in-person training
- Professional development through exposure to clinical research management
- Access to LinkedIn Learning courses covering Outlook, Microsoft Office, Microsoft Project, and project management
- Access to Box University
- Access to REDCap tutorials