Clinical Data Management Analyst

JOB DESCRIPTION:

About Abbott

Abbott is a global healthcare leader creating breakthrough science to improve peoples health. Were always looking towards the future anticipating changes in medical science and technology.

Working at Abbott

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

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

• Employees can qualify forfree medical coverage in ourHealth Investment Plan (HIP) PPOmedical plan in the next calendar year.

• An excellent retirement savings plan with a high employer contribution

• Tuition reimbursement the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelors degree.

• A company recognized as a great place to work in dozens of countries worldwide 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 the best place to work for diversity working mothers female executives and scientists.

The Opportunity

The Clinical Data Management Analyst will be an individual contributor that works under limited supervision and applies subject matter knowledge. Requires the capacity to understand specific needs or requirements to apply skills/knowledge. This is an on-site position in Alameda California.

What Youll Work On

The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs.

• Processes reviews and receives patient data and records and organizes clinical data forms from particular therapeutic groups and outside investigators.

• Provides accurate timely and consistent clinical data to the medical department and other groups.

• Responsible for data management plans including data preparation data validation activities etc.

• Follows Good Clinical Practices (GCP) data-handling procedures and guidelines.

• Requires knowledge of drug and disease terminology.

• May manage service providers that perform these activities.

• Participates in the review of clinical research protocols reports and statistical analysis plans.

• Involvedin the preparation of all applicable data management documents required for the conduct of the study (such as Trial Master File (TMF) Case Report Forms and Data Management Plans).

Required Qualifications

• Associate degree in life sciences or appropriate degree.

• BS degree preferred in life sciences with a minimum of one year of experience in clinical data management or combination of appropriate education and experience.

• Demonstrated excellence in teamwork shared mindset for success stellar interpersonal and communication skills including building rapport with team members peers and management.

• Solid understanding of the clinical trial process including study design and conduct; clinical data management systems; clinical trial management systems; data analysis; and data reporting and interpretation.

• Must have a demonstrated ability to solve problems with innovative solutions along with strong project management and organizational skills to deliver projects on time and on budget.

• Able to manage numerous projects/conflicting priorities and to be flexible when priorities change.

• Experience using Electronic Data Capture systems Veeva Vault eTMF and SAS.

• Working knowledge of GCP GCDMP Clinical and Regulatory Affairs.

• Flexibility in daily activities.

The base pay for this position is

In specific locations the pay range may vary from the range posted.

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