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. You'll also 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, the student debt program and education benefit - an affordable and convenient path to getting a bachelor's degree.
• A company recognized as a great place to 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. Whether it's glucose 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 than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine finger sticks.

The Opportunity

Our location in Maple Grove, MN currently has an on-site opportunity for an Associate Clinical Data Manager. The Associate Clinical Data Manager is responsible for performing data management tasks within defined established processes throughout the life cycle of the study including startup, conduct and reporting phases.

What You'll Work On

Works with Data Review Manager in the study start-up and planning, including contributing to the development of the Risk Assessment and Risk Mitigation Plan, Data Management Plan, Central Monitoring Plan and Data Review Plan. Translates Clinical Study requirements into technical requirements for eCRFs, edit checks, study notifications and customizations in the study database in close collaboration with other member of the data review team. Able to develop CRF with cross functional support, incorporating appropriate feedback and finalizing the CRF. Able to develop specifications for data listings for continuous data review, and communicate with data analytics team members through their development and release. Able to work with external non-CRF data, including creating Data Transfer Specifications, verification of external data structure for import into the data model. Able to develop edit check specifications to review for illogical, incomplete and inconsistent data including testing and troubleshooting of edits checks. Identifies, analyzes, proposes and effectively resolves complex data/database structure issues by exercising appropriate judgment and collaborating with the clinical project team members and other shared service functions. Contributes to the development and maintenance of Clinical Database systems, including EDC, Edit Checks, Reporting, Study Notifications, etc through the following: Partner closely with Data Review Management, Study Database Manager, and Data Analytics and Systems and other Data Review team members. Perform and document functional and/or user acceptance testing on study databases, reports, study notifications, and database customizations. Utilize existing tools/reports, SQL, and database UI to identify data issues and drive resolutions with the Clinical Study Team in a timely manner. Attend Clinical Study Team meetings. Contribute technical expertise to cross functional teams through CRF changes and the impact on databases and propose implementation strategies. Assists in FDA and Quality System audits that involve Clinical Database and Data Management. Follows data management standards and best practices and assures standard processes are followed for Data Management activities. Contribute to data cleaning and data snapshot efforts for regulatory submissions and other business needs as requested by the Clinical Study Team through the following: Generate database snapshot and prepare datasets for Biometrics. Contribute to data review meetings with the Clinical Study Team and Biometrics to identify data cleaning issues and strategize cleaning efforts. Monitor overall data management tasks to ensure timelines are met and any issues are proactively identified and resolved. Perform other duties as assigned.

Required Qualifications CAN'T CHANGE

• Bachelor's degree in a related field OR an equivalent combination of education and work experience.
• Minimum 3 years' in clinical, medical or research setting.
• Education and work experience in computer science, life sciences or technical field.
• Knowledge of data collection best practices for clinical trials.
• Knowledge of global clinical operations.
• Intermediate therapy specific knowledge of anatomy, physiology, pathophysiology, therapy and device.
• Intermediate medical knowledge related to common medical histories, medical terminology, diagnostics (imaging, laboratory), and medications (class, dose, route).
• Certified Clinical Data Manager (CCDM) or equivalent.