Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals.  We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

You will join a widespread, yet closely-knit team with the same mentality and desire to develop smart and intelligent approach to project monitoring. You will help to shape the future of effective risk-based monitoring at PSI and ensure higher quality of study data. You will spend time monitoring study data remotely, identifying errors and issues with site performance. 

Hybrid position after trial period.

You will:

Review EDC, IxRS, Laboratory and other vendors’ data and clinical listingsIdentify single errors and systematic issues related to site performanceGenerate, follow up and resolves data queries and site issuesIdentify and record protocol deviationsAssist to Central Monitoring Manager with administrative activities, including managing study data, documents and reportsEnsure site monitors receive information on site related risk & issues. Escalate findings to study teamsAssists with root cause investigation and follow up on site performance signals identified during central monitoring review

QualificationsCollege/University degree or an equivalent combination of education, training & experiencePrior experience in Clinical ResearchExperience in central monitoring and clinical data review is a plusFull working proficiency in EnglishProficiency in MS Office applicationsAnalytical mindset and attention to detailAbility to learn, plan and work in a dynamic team environment

Additional Information

Make the right call and take your career to a whole new level.  Join the company that focuses on its people and invests in their professional development and success.