Associate Clinical Data Manager

Working at Abbott

At Abbott you can do work that matters grow and learn care for yourself and family be your true self and live a full life.Youllalso have access to:

• Career development with an international company where you can grow the career you dream of.

• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.

• An excellent retirement savings plan with high employer contribution

• Tuition reimbursement theFreedom 2 Savestudent debtprogramandFreeUeducation benefit - an affordable and convenient path to getting a bachelors degree.

• A company recognized asa great placeto work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.

• A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity working mothers female executives and scientists.

For years Abbotts medical device businesses have offered technologies that are faster more effective and less invasive. Whetheritsglucose monitoring system innovative therapies for treating heart disease or products that help people with chronic pain or movement disorders our medical device technologies are designed to help people live their lives better and healthier. Every day our technologies help more than10000 peoplehave healthier hearts improve quality of life for thousands of people living with chronic pain and movement disorders and liberate more than500000 peoplewith diabetes from routinefingersticks.

The Opportunity

Our location inMapleGroveMNcurrently has an on-site opportunity for anAssociate Clinical Data Manager.As the customer-face oftheData Reviewteamand its primary liaison with theClinicalprojectteam theAssociateClinical Data Managers in-depthclinical operations andtherapy-specific knowledge ensures alignment to customerneeds andinforms review and analysis of study data.

WhatYoullWork On

• Leads andfacilitatesan ongoing evaluation of risk involving in-depth review of protocol and plan documentation discussion and validationrisk-related findings with cross-functional workgroup and the development of systems and process-based controls to mitigateidentifiedrisks. These responsibilities include:

• Leading cross-functional teams during protocol development toidentifyand document those data which are critical to the reliability of study results and the protection of human subjects

• Managing the development and revision of the critical processes (e.g.CRF design Edit Checks data listings and clinical database setup) by which those data will be captured and managed throughout the clinical investigation

• Identifyingand evaluating residual risks to critical study data and supervising the development ofadditionalmitigations including focused data cleaning and quality activity targeted site instruction and study-specific Central and Site Monitoring plans

• Leads the Clinical Project Team through the development of Case Report Forms and partners with the Study Database Manager through study database development and release includingidentifyingprogrammingand testing edit checks.

• Conducts complex review and analysis of subject data as it accumulates resolving discrepant or aberrant data points via individual queries to study sites as well as the identification of systemic and/or significant data quality issues requiring escalation; manages escalation efforts and drives them to resolution in partnership with Project Management Site Management Clinical Science Biometrics Safety and organizational leaders.

• Manages progress towards data cleaning and data freeze/lock targets for regulatory submission and other business needs asidentifiedby the Clinical Project Team.

• Manages with dedicated support of the Clinical Data Coordinator the study-wide issuance and resolution of discrepancies over the study lifecycle.

• Overseesthe maintenance of data review standards and best practices ensuring adherence informed by therapy-specificexpertise.

• Leads proactive partnership on both an ad hoc and period/prescribed basic with field and study team personnel presenting findings and issues uncovered during data review devising and documenting appropriate resolution and escalation strategies and managing the overall health of data quality and study conduct through milestones and deliverables over the lifecycle of the study.

Required Qualifications

• Bachelors degree in a related fieldOR an equivalent combination of education and work experience.

• Minimum 4yearsrelated workexperiencewith a solid understanding of specified functional area.

• Broad knowledge and application of business conceptsproceduresand practices.

• Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations.

• Learnsto use professional concepts and company policies and procedures to solve routine problems.

• Works on problemsoflimited scope.Independent decision making.

PreferredQualifications

• Bachelorsdegree inbusiness administration datasciencestatisticsor life sciences.

• 3-5 years experience inclinical operations or healthcare related field

• Strong verbal and written communications withabilityto effectively communicate at multiple levels in the organization.

• Excellent analytical skills and ability to manage complex tasks and manage time effectively.

• Prior data management experience.