Piedmont Healthcare Inc.
Clinical Study Coordinator
US, Washington · Contract
Sponsorship not specifiedDetected 15 days ago
GCPAccessibilityClinical TrialsClinical ResearchResearchCommunicationCollaborationGxP
About the role
- Your Profile: You will bring relevant clinical research experience, along with the following qualifications and skills.
- Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
- Inclusion and Accessibility ICON is an equal opportunity employer.
Responsibilities
- Completing and maintaining study regulatory binder and documents including, but not limited to, training documentation, screening and enrollment logs, and investigational product accountability and device usage logs.
- Perform a secondary completeness and accuracy check of each paper CRF prior to data entry.
- Transcribe all data from the paper source documents into Medidata in a timely manner.
- We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
Requirements
- Bachelor's degree in a relevant scientific discipline.
- Proven experience as a Clinical Study Coordinator or in a similar role.
- Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
- All study data must be de-identified and verified by the site prior to upload into Medidata.
- Source data for research-specific procedures must be recorded on paper at the time the procedure is performed.
- These templates must be used to capture source data for subsequent transcription into Medidata.
Compensation
- Competitive base salary and performance related incentives
Benefits
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
- Visit our careers site to read more about the benefits ICON offers.
- Scheduling and issuing reminders for follow-up visit(s), and completing follow-up medical history documentation, within three (3) months post-delivery.
Equal opportunity
- ICON is an equal opportunity employer.
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