Clinical Data Reviewer

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.
You will:

Review clinical data remotely and identify errors, systemic issues and trends related to data integrity, participant safety and site performance

Generate, follow up and resolve data queries and site issues, and identify potential protocol deviations

Develop and maintain study-specific Central Data Review tools, templates and tracking materials

Support the setup and management of risk-based and central monitoring tools and activities

Assist with central monitoring signal review, root cause investigation and follow-up

Support the Central Monitoring Manager with study data, documents and reports

Contribute to inspection readiness, including eTMF QC and study archive activities

Bachelor’s degree

At least 1 year of experience in the Clinical Research Industry

Clinical Monitoring experience is an advantage

English proficiency at CEFR B2 level or above

Proficiency in MS Office applications

Analytical mindset and attention to detail

Ability to learn, plan and work effectively in a dynamic team environment

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.
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 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
Originally posted on Himalayas