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Skills
Certified Public Accountant (CPA)unmatched
Clinical Dataunmatched
Clinical Informationunmatched
Clinical Information Systemsunmatched
Clinical Trainingunmatched
Clinical Trial Managementunmatched
Data Qualityunmatched
Employee Retentionunmatched
FDA Requirementsunmatched
GCP (Good Clinical Practices)unmatched
Logisticsunmatched
Microsoft Excelunmatched
Microsoft PowerPointunmatched
Microsoft Wordunmatched
On Site Supportunmatched
Organizational Skillsunmatched
People Managementunmatched
Plan Meetingsunmatched
Presentation/Verbal Skillsunmatched
Quality Assuranceunmatched
Registered Nurse (RN)unmatched
Spreadsheetsunmatched
Staff Trainingunmatched
Standard Operating Procedures (SOP)unmatched
Talent Managementunmatched
Team Playerunmatched
Word Processingunmatched
Description
Clinical Project AssociateIntegrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.Job Description• Must meet all requirements for CPA grade 24 position and have demonstrated proficiency in all relevant areas• Provide input and assist with harmonization of Clinical Operations databases and tracking tools• Assist in maintaining clinical information and training of Clinical Operations personnel in the clinical trials management system (GILDA)• Serves as CTMA back up providing verbal and written communication with study personnel• Tracks and prepares study-specific information utilizing databases, spreadsheets, and other tools• Reviews and participates in the quality assurance of data or documents• Arranges meeting logistics, agendas and assists with minutes• Interacts with other departments, as directed, to complete assigned tasks• May assist with monitoring visits under the direct supervision of senior staff• Assists with the planning and facilitation of investigator meetings and, when applicable, provides onsite support during the meetings• Knowledge of FDA and EMA Regulations, ICH Guidelines, GCP, and familiarity with standard clinical operating procedures• Must be familiar with Word, PowerPoint, and Excel• Travel may be requiredQualifications• At least 1+ year of experience and a BS or BA in a relevant scientific discipline• At least 1+ year of experience and an RN (2 or 3 year certificate)Other Details:• Ability to take direction from senior team members• Collaborative demeanor• Great organizational skills• Strong computer technical skills with regards to word processing and spreadsheet development• Looking for someone:Task orientedForward thinkingOrganized1-2 years of relevant experience or in similar role