Reference Number:
DF-CRASTLMO

Job Description:
Seeking CRA's All over the USA! Please send an updated resume to danielle@sunrisesys.com with Ref# DF-CRASTLMO

Demonstrate exceptional customer focus as evidenced by positive feedback from colleagues and external customers (Investigators).
Participate in the site nomination process; perform evaluation of site capability to deliver the contractually agreed to number of patients and high quality data then make recommendation for inclusion in the clinical trial.
Assume ambassadorial role to facilitate communication between sites and line functions to increase value proposition to investigators.
Facilitate preparation and collection of site level documents.
Execute site initiation and training activities.
Perform monitoring visits according to monitoring plan and author study monitoring reports.
Manage site drug supply management.
Resolve site level update of technical systems (ClinAdmin, EDC).
Ensure site activities in line with milestones (i.e. startup, recruitment, closeout, etc).
Manage recruitment implementing appropriate contingency plans as needed.
Assure continual GCP, ICH and SOP compliance (Informed consent process, source data verification, AE and SAE reporting, IN, protocol, drug accountability etc.).
Resolve deviations to standard by remedial action and training.
Perform data query resolution process (both at Site and with Data Management).
Execute site closeout activities.
May act as local (or global) CRA Lead, as assigned.

Experience Level:
4 Years

Requirements:

Location:
East Hanover NJ

Duration:
6 - 9 months

Pay Rate: