Clinical Data Reviewer at PSI CRO

Ciudad de México, , Mexico -

Full Time

Start Date

Immediate

Expiry Date

02 Jan, 26

Salary

0.0

Posted On

04 Oct, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Data Review, Analytical Mindset, Attention To Detail, MS Office, Risk-Based Monitoring, Protocol Deviations, Central Monitoring, Data Queries, Site Performance, Problem Solving, Team Collaboration, Communication, Root Cause Investigation, Study Data Management, Administrative Activities

Industry

Pharmaceutical Manufacturing

Description

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. You will: Review EDC, IxRS, Laboratory and other vendors’ data and clinical listings Identify single errors and systematic issues related to site performance Generate, follow up and resolves data queries and site issues Identify and record protocol deviations Assist to Central Monitoring Manager with administrative activities, including managing study data, documents and reports Ensure site monitors receive information on site related risk & issues. Escalate findings to study teams Assists with root cause investigation and follow up on site performance signals identified during central monitoring review Qualifications College/University degree or an equivalent combination of education, training & experience Prior experience in Clinical Research Experience in central monitoring and clinical data review is a plus Full working proficiency in English Proficiency in MS Office applications Analytical mindset and attention to detail Ability 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.

Responsibilities

You will review clinical data and identify errors related to site performance. Additionally, you will assist in managing study data and resolving site issues.