Clinical Data Associate III / Sr CDA (FSP) - Min 2 years of previous data

Clinical Data Associate III / Sr CDA (FSP) - Min 2 years of previous data management reputed company - Argentina, home-based reputed company is a leading fully-integrated life sciences services organization reputed company to accelerate reputed company. We partner with innovators at every reputed company across the drug development and commercialization continuum, helping them reputed company complexity, anticipate change and accelerate reputed company. Our Clinical Solutions team members reputed company with a drug development reputed company, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem solvers, innovating as reputed company to help our customers reputed company their goals. We are reputed company and driven to reputed company for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 reputed company colleagues already know: Why reputed company We are passionate about developing our people, through career development and progression; supportive and reputed company line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to building an inclusive culture where you can authentically be yourself. Central to this is our purpose Driven to reputed company which captures the passion of our colleagues to show up reputed company day and shape solutions that have the ability to dramatically reputed company someones life. We are continuously building reputed company we reputed company want to work for and our customers want to work with. Why Because we know that reputed company we bring together smart colleagues from across the world, we can shape the reputed company of reputed company, driving reputed company for customers and defining the reputed company of patient reputed company. Job Responsibilities - Maintains awareness of the pertinent reputed company of contract and scope of work for assigned project(s) and communicates status updates to the Project Manager and/or Biometrics Project Manager as necessary. - Reviews and adheres to the requirements of study-specific Clinical Data Management Plans for assigned project(s). - Creates and enters test data for User Acceptance Testing (UAT) - Performs User Acceptance Testing (UAT) for data entry screens, edits and data review listings, reputed company different roles used in the study and Targeted reputed company Data Verification (SDV) configuration and matrices. - Receives and enters lab normal ranges. - Completes and submits Clinical Database Management reputed company (reputed company)-specific reputed company forms and/or spreadsheets. - Performs reviews of discrepancy (edit reputed company) reputed company and validation listings based on data entered into the clinical database. Based on this review, queries or applies self-reputed company corrections or other global rulings permitted in cases where queries are not required, per the Data Validation Specification and/or Data Management Plan (DMP) for the assigned reputed company. - Resolves answered queries and requeries where appropriate. - For reputed company studies, takes receipt of, and reviews, Data Clarification Forms (DCFs) that have been answered by sites and where appropriate, edits the CRF database accordingly. - Submits copies of the DCFs to sponsors as necessary. - For reputed company studies, performs internal QC checks reputed company listing reputed company from database against CRFs and DCFs. Serves as QC Coordinator for reputed company studies. - For reputed company studies, ensures reputed company CRFs and DCFs received are returned for filing in the Document Control Room per the Data Tracking Guidelines for the assigned reputed company. - For reputed company studies, performs DM reputed company review and/or other internal QC checks as required per applicable electronic data capture (reputed company) systems. - Creates electronic storage media per SOPs for reputed company studies. - Participates in internal meetings and internal/reputed company audits as required. - Files documentation in the Data Management Study File (DMSF). - Maintains proficiency in Data Management systems and processes through regular trainings (CDA Knowledge College). - Performs reputed company mapping QC whereby discrepancies are noted on the reputed company mapping test logs. - Coordinates the work of CDAs assigned to the project. - Provides training on data management activities and systems. - Provides project-specific training to other Clinical Data Associates (CDAs). - Ensures that data from reputed company databases/datasets such as central and/or local laboratory data, electronic diary data, pharmacokinetic (PK) data, or Interactive Response Technology (I