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Clinical Research Associate Jobs

Company

Jobot

Address Germantown, MD, United States
Employment type FULL_TIME
Salary
Category Staffing and Recruiting
Expires 2023-08-06
Posted at 9 months ago
Job Description
Want to learn more about this role and Jobot? Click our Jobot logo and follow our LinkedIn page!


Job details


Clinical Research Associate opportunity in the oncology space!


This Jobot Job is hosted by Audrey Block


Are you a fit? Easy Apply now by clicking the "Apply" button and sending us your resume.


Salary $100,000 - $120,000 per year


A Bit About Us


Prep-Ipo Biotech company with strong funding, focused in the Oncology space. We are looking for 1-2 Senior CRA's to join our team!



Why join us?


Opportunity to wear different hats in a small company-lots of growth!


Exciting science in the oncology space


Strong Benefits And Compensation Package


401k with a match


Pre ipo stock options


Job Details


Looking for 1-2 Senior CRAs to join the team! Oncology experience is REQUIRED. Please note-this position requires domestic travel about 50% of the time!


Develops strong investigative site relationships and ensures continuity of investigative site relationships through all phases of the trial


Conducts site visits including but not limited to Pre-study visits, initiation visits, interim monitoring visits, close-out visits to ensure compliance with protocols, Sponsor SOPs, ICH/GCP and all applicable regulations


Performs remote and on-site monitoring & oversight activities using various tools to ensure data generated at the site are complete, accurate, and unbiased; subjects' rights, safety, and well-being are protected


Collects, reviews, and monitors required regulatory documents for study start-up, study maintenance, and study close-out


Communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, missing data and data queries, protocol deviations, regulatory documentation, site audits/inspections, and overall site performance


Identifies, assesses, and resolves site performance, quality, or compliance problems and escalates per protocol to upper management


Work with in-house Clinical Trial Assistant to collect, review, and monitor required regulatory documentation for study start-up, study maintenance, and study close-out.


Manages and maintains information and documentation in Clinical Trial Management System, electronic Trial Master File, and various other systems as appropriate and per timelines


Interested in hearing more? Easy Apply now by clicking the "Apply" button.


Want to learn more about this role and Jobot?


Click our Jobot logo and follow our LinkedIn page!