Assoc Site Report Specialist
Assoc Site Report Specialist
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Job Description
Job Overview
Review Site Visit Reports (SVRs) to ensure they meet or exceed quality standards and support goals of quality subject safety data integrity and regulatory compliance. Use tools and techniques to ensure the efficient and effective review of Site Visit Reports and their associated attachments in compliance with IQVIA SOP ICH/ GCP guidelines and protocol requirements
Essential Functions
Oversee a caseload of SVRs for assigned studies ensuring compliance to the protocol processes timelines IQVIA/applicable SOPs and GCP guidelines.
Review SVRs to ensure findings requiring corrective and /or preventative action plans are documented and followed up to resolution to ensure high quality reports.
Participate on the project team for all SVR review activities and identifies and escalate CRA and /or site issues relevant trends and related risk factors to the project team and appropriate parties in a timely manner to optimize quality of project delivery.
Provide guidance to Clinical Project Managers (CPMs) at project start-up and throughout the study and partner with the project team members to decrease the level of corrections/additions needed on reports by providing insight and training of the SVR annotations.
Identify and track the project team compliance to SOPs for submission and approval of the SVRs through communication with the CRAs and line managers.
Participate in meetings with project team to discuss any SVR review issues illustrative of quality/performance deficiencies across PIs/sites and CRAs. Assist with identification of the trends emerging from the Issue Escalation Log.
Provide coaching to CRAs to decrease the level of corrections/additions needed on reports.
Provide quality improvement support such as quality checks data trending providing back up support and mentoring and coaching of junior staff members.
May take on special project assignments related to function/corporate initiatives.
Qualifications
Bachelors Degree Healthcare or other scientific discipline or educational equivalent Req
7-8 years of Clinical Research experience including a minimum of 3 to 4 years on-site monitoring experience Req Or
Equivalent combination of education training and experience. Req
Strong knowledge of and skill in applying applicable clinical research regulatory requirements; i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Through knowledge and understanding of the Clinical monitoring processes and sound knowledge of clinical trial systems and applications
Demonstrated skill in understanding and executing complex study designs as well as multiple studies
Strong written and verbal communication skills.
Effective time management and organizational skills and the ability to manage competing priorities
Ability to work independently with good analytical and problem solving skills
Demonstrated ability to work across cultures and geographies with a high awareness and understanding of cultural differences
High quality orientation with a focus on attention to detail
Ability to establish and maintain effective working relationships with coworkers managers and clients.
Fluent in English both spoken and written.
IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
Required Experience:
Unclear Seniority
Employment Type
Full-Time
