You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.
You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).
As a CRA, you will work with 2-3 protocols on average and support Project Managers with trials that are larger in scope.
You will interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations.

Requirements

4-year college degree or equivalent experience
2+ years CRA experience within the CRO to be considered for a CRA II.
Experience in monitoring cardiology or Lupus
Availability for domestic travel including overnight stays, up to approximately 50-60% travel commitment (potential international travel may be required for some senior level positions)
Fluency in English and for non-English speaking countries the local language of country where position based.

Benefits

Health insurance
401(k) matching
Paid time off
Volunteer time off
Paid parental leave

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard skills

clinical study monitoringregulatory submissionsprotocol adherenceSOPsICH-GCPclinical trial managementdata reportinginvestigator identificationpre-study visitsinitiation visits

Soft skills

client interactionpresentation skillsorganizational skillscommunication skillsteam collaboration