Clinical Data Associate

2 months ago

Bengaluru Karnataka, India Alcon Full time

Provide timely and professional ongoing management of Data Management deliverables and of clinical trial data with respect to quality, timelines and costs for assigned trials within Clinical Data Management. Ensure consistently high quality data available for analysis and reporting.

Provides DM support across assigned trial(s).

Provides feedback to assure well-developed databases and data validation setup and execution while making the best use of standards and best practices

Supports the team through database build requirements and complete startup activities for study including: building the eCRF, completion guidelines, standard and simple rules, data validation plan and user acceptance testing (UAT); can lead a study in sequence under PCDM supervision.

Set up and Manage external data in accordance with protocol requirements, process and validation requirements

Performs DM maintenance and validation activities during the course of the study timely and with quality.

Tracks and reports status and progress for assigned trials and projects. Is proactive to ensure milestones are met with quality (incl. Snapshots and interiM/Final locks).

Effectively communicates status updates and study level information to the Trial Data Manager (TDM) and Program Clinical Data Manager (PCDM)

Provides support to business users and teams on their use and supporting the implementation of the Clinical Data Standards strategy.

Ensures adherence to GCP, DM standards, SOPs/procedures, job aids and guidelines

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Alcon is an Equal Opportunity Employer and takes pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital status, disability, or any other reason.

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