CPC este o companie de suport și servicii IT care ajută organizațiile să mențină medii tehnologice fiabile și sigure. Fondată în 1962, compania îmbină expertiza în inginerie și consultanță cu vânzarea, mentenanța și asistența pentru hardware și software de calculator noi, second-hand și recertificate în fabrică. Soluțiile sale deservesc companii cu sau fără echipe IT interne, din domeniile sănătății, logisticii, consultanței, muncii la distanță și producției. CPC colaborează cu furnizori de tehnologie precum Citrix, IGEL, LG, Nutanix, Arctic Wolf, NoMachine, Zebra Technologies și Dell, oferind clienților soluții practice pentru infrastructură și tehnologia spațiului de lucru. Contextul angajărilor reflectă o echipă concentrată pe furnizarea unor operațiuni IT eficiente și a unui suport tehnic de încredere.
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.
Descriere
- 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
Cerințe
- 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
Beneficii
- 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