Abbott
healthcare
ClinicalDataManagementAnalyst
“Clinical Data Management Analyst at Abbott. Skills: clinical data management, data processing, data review, data organization, data validation. 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”
What You'll Achieve.
deliver projects on time and on budget
Industry & Context.
solve problems with innovative solutions
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Travel: Yes, 10 % of the Time
What They're Looking For.
Must Have
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 clinical data management clinical trial management data and data reporting and interpretation, Must have a demonstrated ability to solve problems with innovative solutions along with 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
Nice to Have
BS degree preferred in life sciences
What You'll Do.
and receives patient data and records and organizes clinical data forms from particular therapeutic groups and outside investigators
and consistent clinical data to the medical department and other groups
Responsible for data management plans including data preparation
data validation activities
Follows Good Clinical Practices (GCP) data-handling procedures and guidelines
May manage service providers that perform these activities
Participates in the review of clinical research protocols
reports and statistical analysis plans
Involved in 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)
How You'll Work.
Team & Collaboration
building rapport with team members, peers, and management
Communication Scope
communication skills
Process & Methodology
project management, organizational skills, deliver projects on time and on budget, manage numerous projects/conflicting priorities
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