In-House CRA and Unblinded CRA with experience various clinical trials, mainly focused on oncology trials.
To seek and maintain a full-time position that offers professional challenges utilizing interpersonal skills, excellent time management and problem-solving skills.
Overview
11
11
years of professional experience
4
4
years of post-secondary education
3
3
Languages
Work History
Unblinded Clinical Research Associate
Fortrea Inc (former LabCorp)
07.2023 - Current
Conducted on-site monitoring visits to verify study procedures, regulatory documents and data completion.
Acted as a primary contact for the sites.
Verified drug accountability, drug reconciliation, TMF reconciliation at the site.
Performed remote and face-to-face site staff trainings.
Prepared accurate and in timely monitoring visits reports.
Independently perform CRF review; query generation and resolution against established data review guidelines
Provided sites with document updates and trainings as appropriate.
Collaborated with cross-functional teams to successfully meet project timelines and deliverables.
In-house Clinical Research Associate
Fortrea Inc (former LabCorp)
11.2022 - Current
Collaborated with clinical study site and sponsor to troubleshoot and provide solutions to study-related issues.
Conducted thorough site feasibility assessments for potential clinical trial participation, identifying suitable sites for studies.
Reviewed data queries and listings and worked with study centers to resolve data discrepancies.
Collaborated with cross-functional teams to successfully meet project timelines and deliverables.
Performed site management, TMF management, CTMS management and payment process activities.
Provided sites with documents updates.
Performed co-monitoring visits.
Clinical Research Coordinator
East Tallinn Central Hospital
02.2018 - Current
Completed paperwork, recognizing discrepancies and promptly addressing for resolution.
Used critical thinking to break down problems, evaluate solutions and make decisions.
Maintained compliance with protocols covering patient care and clinical trial operations.
Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
Safety Science Analyst- Post Marketing Safety at Fortrea (Previously As LabCorp)Safety Science Analyst- Post Marketing Safety at Fortrea (Previously As LabCorp)