Sr clinical data scientist cdm (hybrid - argentina)updated: april 23, *location: tlalnepantla, mex, mexicojob id:*-othloc-*dhdescriptionsenior clinical data scientist to lead and coordinate clinical data science activities for phase 3 clinical trials.
this role requires managing data quality, risk assessment, data acquisition planning, and cross-functional coordination to ensure timely and compliant data deliverables.job responsibilitiesserve as functional lead for clinical data science, primary contact between clinical data science, project management, clinical monitoring, and other functional groups.act as central steward of clinical data quality, monitor risks through holistic review of clinical and operational data.identify required data elements and data quality oversight steps to support defined study analysis.communicate, troubleshoot, and resolve data-related questions with project teams, escalating patient safety or study analysis impact issues.coordinate cross-functional data cleaning activities to meet quality standards and timelines.drive development of clinical data acquisition plans, data flow diagrams, assess protocol risks, and ensure data collection meets regulatory and study endpoint requirements.develop and utilize analytical tools and dashboards to detect potentially unreliable data.perform analytic reviews, identify root causes, and systematically resolve data issues.monitor and communicate project progress to sponsor and project team using status reports and metrics.ensure completion of all clinical data science activities and milestones per contractual agreements and sops.review and maintain budget; identify out-of-scope activities and initiate change orders.plan, manage, and request resources for assigned projects.coordinate work of the assigned clinical data science team.develop and maintain project plans, specifications, and documentation per sops.maintain tmf filing and ensure up-to-date documentation.participate in and present at internal, sponsor, third-party, and investigator meetings.contribute to proposal bid defense meetings and rfps.support internal and external audits and prepare necessary documentation.train and mentor new or junior team members.maintain proficiency in clinical data science systems and processes through regular training.attend professional meetings and conferences on behalf of the company (travel up to 25%).
perform other work-related duties as assigned.qualificationsexperience in clinical data science within drug development, particularly in managing data quality and regulatory compliance.strong understanding of clinical protocols, therapeutic area nuances, and data acquisition planning.proficiency with analytical platforms, dashboards, and statistical analysis to identify data issues.excellent communication skills to liaise with cross-functional stakeholders and sponsors.experience in project management, including budgeting, resource planning, and timeline coordination.knowledge of sops, regulatory guidelines, and tmf requirements.ability to train and mentor team members and sustain proficiency through continuous learning.minimum travel requirement of up to 25%.
additional informationthe company reserves the right to assign other tasks, duties, and responsibilities to the incumbent as deemed necessary.
equivalent experience, skills, or education may be considered in lieu of the above qualifications.
the company is committed to compliance with the americans with disabilities act and the eu equality directive, and it will provide reasonable accommodations as appropriate.summaryresponsible for end-to-end coordination of cross-functional data collection and cleaning activities to ensure clinical study data deliverables are fit for purpose and align with contract and sponsor expectations and timelines.
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