Manager, Clinical Data Review

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

We are looking for our nextManager Clinical DataReviewto lead our team on-site out of our Maple Grove MN.As a manager the individual has primary management responsibility directly or through subordinates for all data related to clinical studies. This new team member will have accountability for all data entry activities Case Report Form (CRF) design edit check specifications and other requirements of the Clinical databases providingdatasetsand performing data cleaning for analysis. Additionallywillidentifyand routinely use the most effective cost efficient and best business practice to execute processes; continually evaluate their effectiveness and appropriateness. The Manager Clinical Data Review will exercise judgment in planningorganizingand performing work;monitorperformance and report statuses to executive management as well as assures that quality of services meets internal and external customer requirements. The individual will remain current on developments in field(s) ofexpertiseto ensure that clinical trial protocol elements are appropriately captured on CRFs and databases for analysis; responsible for ensuring database integrity.

WhatYoullWork On

Responsible for hiring andretaininga diverse highly qualified data management staff and for providing career coaching growth and personal development. Accountable for staff development: critiquesinstructs mentorsevaluates and coaches. Ensures staff is appropriately trained in processes and procedures; ensures established processes and procedures are being followed and documented. Accountable for the performance of subordinates and work output of managed subcontractors. Maintains a safe work environment and a strong customer focus.Modelsoptimumleadership competencies to inspire an energizedempoweredand accountable work force ethical behavior favorable community image and actualization of theAbbottGuiding Principles and values.

Manages data entry data cleaning data deliverables and other data management activities.

Oversees the development of CRFs edit check specifications andadditionaldata collection requirementsfor tracking and analysis.

Manages the implementation and execution of Risk-Based Quality Management (RBQM) activities including risk assessments risk mitigation plans data review strategies centralized monitoring activities and Key Risk Indicator (KRI) oversight

Manages processes to ensure data integrity via appropriate data management processes (e.g. protocol compliance reporting querying for missing or discrepant data evaluating data outliers performing data quality checks etc.).

Monitors operational performance and quality indicators;identifiestrends risks and opportunities for improvement andimplementscorrective actions as needed.Remains current on developments in field(s) ofexpertise regulatory requirements and industry trends and trains staffregardingchanging regulations that affect clinical studies. Maintains knowledge of current and pending regulations through literature trade journals professional associations and by attending conferences.

Hires andretainsa diverse highly qualified staff and provides ongoing performance feedback. Sets goals which align to department plans andmanagesthe execution of goals through coaching and mentoring. Maintains a safe and professional work environment.

Support all Company initiatives asidentifiedby management and in support of Quality Management Systems (QMS) Environmental Management Systems (EMS) and other regulatory requirements.

Complies withU.S. Food and Drug Administration (FDA) regulations other regulatory requirements Company policies operating procedures processes and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees customers contractors and vendors.

Required Qualifications

Bachelors degree in a science-related field or an equivalent combination of education and experience

Minimum 8 years progressively more responsible experience in the pharmaceuticalbio-technologyor medical device industry; must be able to apply the fundamental concepts and practices to conduct needs assessment research and develop information for market development purposes.

Advanced computer skills in graphics word-processing databases authoring programs etc.

Advanced personal computer skills (experience with Microsoft Office or equivalent required) in graphics word-processing databases authoring programs etc

Experience working in a broader enterprise/cross division business unit model preferred. Ability to work in a highly matrixed and geographically diverse business environment. Strong leadershipskillsincludingthe ability to set goals and provide positive and constructive feedback respectfully to build positive relationships and improve business results. Ability to work effectively within a team in a fast-paced changing environment. Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization. Multi-tasks prioritizes and meets deadlines in timely manner. Strong organizational planning and follow-up skills and ability to hold others accountable.

Ability to travel approximately 20% including internationally.

Preferred Qualifications

Experience working in a broader enterprise/cross division business unit model

Learn more about our health and wellness benefits which provide the security to help you and your family live full lives:

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer committed to employee diversity.

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