Sr. Clinical Trial Associate

2 weeks ago


Boston, United States Planet Pharma Full time

MUST HAVE

  • Study Start up
  • Sponsor / Biotech (HIGHLY Preferred)
  • TMF spot check
  • Reviewed monitoring reports
  • Tracking documents for review from CRO
  • Review of Pharmacy Manual
  • Able to perform preliminary document review
  • Highly Organized and "on the ball"


Role summary

The CTA/ iCRA, reporting to the Director, Clinical Operations, will be responsible for supporting the management of clinical trials according to applicable regulations and Good Clinical Practice. This role will assist in effective execution of clinical trials including but not limited to managing startup activities, vendor communication, site management activities, essential document development, tracking of various study-specific tasks/ documents for oversight. This individual will assist the Program Directors and Clinical Project Managers in ensuring that our clinical stage projects achieve our objectives providing quality clinical data within established budget and timelines.


The opportunity

A compelling opportunity for an ambitious CTA/iCRA to support the management of clinical trials and potentially first-in-class therapeutic clinical trials. Innovation and excellence are keystones that will allow the candidate to be succeed in an exciting, fast paced work environment.


Role will provide opportunity for long-term professional growth including development as a global clinical operations team leader within a growth-equity backed company.



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