Sr. Oncology Clinical Research Associate

New York, NY, US • Posted 1 day ago • Updated 1 hour ago
Full Time
On-site
USD $120,000.00 - 140,000.00 per year
Fitment

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Job Details

Skills

  • Clinical Research
  • IPO
  • HATS
  • Google Cloud
  • Google Cloud Platform
  • Auditing
  • Regulatory Compliance
  • Documentation
  • Clinical Trials
  • Management
  • Military
  • SAP BASIS
  • Authorization
  • Law
  • LOS
  • Recruiting
  • Legal
  • Artificial Intelligence
  • Privacy

Summary

Remote Sr. CRA position in the oncology space!

This Jobot Job is hosted by: Audrey Block
Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume.
Salary: $120,000 - $140,000 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!
Strong pipeline
Good benefits and compensation package
401k with a match
Flexible schedule

Job Details

Looking for 1-2 Senior CRAs to join the team! Oncology experience is REQUIRED. Please note-this position requires domestic travel about 30-40% 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/Google Cloud Platform 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 Now" button.

Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, age (40 and over), disability, military status, genetic information or any other basis protected by applicable federal, state, or local laws. Jobot also prohibits harassment of applicants or employees based on any of these protected categories. It is Jobot's policy to comply with all applicable federal, state and local laws respecting consideration of unemployment status in making hiring decisions.

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  • Dice Id: 91113390
  • Position Id: 1880374153
  • Posted 1 day ago
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