Join us on our exciting journey!
IQVIA Real-World Evidence (RWE) teams work with clients to help them collect and use real-world data to generate evidence to meet the needs of regulators, payers, providers, and patients.
Our approach is unique in the industry and is defining the way companies develop and apply real-world evidence for healthcare decision making.
We are collaborative, intellectually curious, entrepreneurial, and constantly looking for opportunities to harness the value of real-world evidence in an evolving industry.
Due to continued growth, we are seeking new brave minds to join our award winning and innovative department.
Job Overview :
Under the direction and guidance of the Real World Late Phase Research Site Management Lead, Line Manager or Project Manager, apply clinical research experience and skills to engage site management / monitoring staff to ensure process and practice methodology is applied consistently and in accordance with project scope and budget, SOPs, policies, good clinical practices and applicable regulatory requirements.
Oversee the work of assigned site management staff, providing advice and guidance to help achieve quality deliverables on site.
Assist with the development of Site Recruitment, SPS Operations and SPS Risk Management Plans.
Ensure that clinical monitoring tasks are conducted in accordance with protocol, process, quality standards and expectations, per contract.
Collaborate with other functional groups within the company such as data management, quality assurance and biostatistics where necessary to support milestone achievement and to manage study issues and obstacles.
Manage and follow study activities through ongoing tracking and review of study progress. Report progress to appropriate SPS management and project management leaders.
Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
Provide input and updates to the Clinical Project Manager regarding the monitoring status and CRA team progress and deliverables.
Act as the first line of escalation for site management questions and issues for their assigned projects.
Conduct co-monitoring and / or assessment visits to ensure the study is being conducted in accordance with the protocol, SOPs, GCP and applicable regulatory requirements.
May act as site visit report reviewer.
May conduct monitoring and / or assessment visits as needed to ensure the study is being conducted in accordance with the protocol, SOPs, GCP and applicable regulatory requirements.
Bachelor's degree in a health care or other scientific discipline.
3 years of monitoring experience, team leadership experience; or equivalent combination of education, training and experience
In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.
Strong written and verbal communication skills including good command of English and French language (C1 level).
Demonstrated team leadership skills.
Excellent planning, organizational and problem-solving skills.
What is in it for you?
Variety of therapeutic areas
Collaborative and supportive team environment
Access to cutting-edge in-house technology
Excellent career development and progression opportunities
Embrace your curiosity and grow your career in an exciting environment where development is a priority.
Think boldly and disrupt conventional thinking.
Enjoy what you do.
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.
We believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a healthier world. Learn more at