Job details
Salary up to $35 an hour job type full-time contract number of hires for this role 4
Qualifications
High school or equivalent (preferred)
Full job description
Clinical research coordinator position within a smoClinical research coordinator will support a research portfolio sponsor-initiated clinical trials across multiple therapeutic areas, including but not limited to: cardiac, neuro stroke, ob/gyn, internal medicine and ophthalmology.
Job duties
Responsible for reviewing and comprehending research protocols.
Assist in recruiting potential subjectsSchedule patients within inclusion criteriaPhone screenpatientsAssist during patient visits.
Coordinates day to day activities of several small scale project(s) or phases of one or more larger projectsCollects project data through interviews, chart review or other methodsMay collect, secure and assist with bio specimen management.
May assist in development of study tools (e.gTracking forms, questionnaires, chart review forms, etc.).
Responsible for data collection and data management inputting into appropriate edc.
If assigned to clinical trial, may work with sponsors/ monitors at clinical sites.
Adheres to compliance and privacy/ confidentiality requirements and standardsAdheres to gcp and compliance regulations for clinical trials.
Assists with and/ or oversees quality assurance of study activities ensures quality data.
May interface with irb and/ or draft portions of irb protocols, amendments, continuing reviews, etc.
May contribute to portions of study presentations* reviews scientific literature and synthesizes and summarizes information.
Qualifications
2+ years of relevant clinical research experience
2+ years as a medical assistant, cna, lvn
Job types: full-time, contract
Pay: up to $35.00 per hour
Schedule:
Monday to friday
Education:
High school or equivalent (preferred)
Work location:
Fully remote
Work location: remote
