Position Details

Salary $54 – $59 USD / year

Type Contract

Experience mid

Exp. Years 2+ years

Education Bachelor’s degree in clinical research, science, or health-related field; or HS diploma with 6 years of clinical research experience

Category Healthcare & Medical

About this role

Temporary CRA II/Field Monitor supporting clinical research teams with training materials, protocol interpretation, document collection, and trial support.

Key Responsibilities

Develop and update training materials
Interpret study protocols
Create site feasibility questionnaires
Collect essential documents during start-up
CRF data review and data query resolution

Technical Overview

Experience with EDC/eTMF/CTMS; strong documentation and regulatory knowledge; remote site coordination across time zones.

Ideal Candidate

The ideal candidate is a mid-level CRA with at least 2 years of post-CRA I experience, proficient in EDC/eTMF/CTMS, and comfortable with remote work and extensive site coordination across time zones.

Must-Have Skills

Bachelor’s degree in clinical researchscienceor health-related field with 4 years of experience in a clinical research setting; or HS diploma with 6 years of experienceMinimum of 2 years’ experience as a Clinical Research Associate IProficiency in MS WordExcelPowerPointOutlookAdobeKnowledge of ICH E6 and CFR

Nice-to-Have Skills

Experience with EDCeTMFCTMSRemote work across multiple time zones

Tools & Platforms

EDCeTMFCTMS

Required Skills

EDCeTMFCTMSICH E6CFRsite initiationCRF data reviewMS WordExcelPowerPointOutlookAdobe

Hard Skills

EDCeTMFCTMSICH E6Code of Federal RegulationsMS WordExcelPowerPointOutlookAdobesite feasibility questionnairesstudy trackers

Soft Skills

Excellent written/oral communicationStrong organizational and multi-taskingIndependent decision makingTeam collaborationDetail oriented

Industry & Role

Industry Healthcare & Medical

Job Function Clinical trial coordination and start-up support for CRA II

Role Subtype Clinical Research Associate II

Keywords for Your Resume

CRA IIClinical Research Associate IIImmunityBioremoteclinical researchsite initiation traininginformed consent form templatesprocedures manualslaboratory and pharmacy manualsICH E6Code of Federal RegulationsEDCeTMFCTMSCRF data reviewsite visitsIP temperature monitoringremote monitoringdata listingsclinical study reportsite initiationinformed consentedcetmfctmsich e6crf data review

Deal Breakers

Less than 2 years CRA experience, No familiarity with EDC/eTMF/CTMS, Unwillingness to travel up to 75% of the time

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IB Temporary – CRA II, Field Monitor

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