Clinical Data Associate Jobs in Minnesota (NOW HIRING)

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.You'llalso 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 bachelor's 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, Abbott's medical device businesses have offered technologies that are faster, more effective, and less invasive. Whetherit'sglucose 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 than10,000 peoplehave healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than500,000 peoplewith diabetes from routinengersticks.

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 Manager's in-depthclinical operations andtherapy-specific knowledge ensures alignment to customerneeds, andinforms review and analysis of study data.

WhatYou'llWork 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, includingidentifying,programmingand 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

• Bachelor's degree in a related fieldOR an equivalent combination of education and work experience.

• Minimum 4years'related workexperiencewith a solid understanding of specified functional area.

• Broad knowledge and application of business concepts,proceduresand 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 makingrequired.

PreferredQualifications

• Bachelor'sdegree inbusiness administration, datascience,statisticsor 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 experiencerequired.