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An established industry player is seeking a Clinical Data Strategist to lead data review activities and develop innovative analytic tools. This role involves mentoring junior staff, ensuring timely data reviews, and communicating with management on study activities. The ideal candidate will possess strong analytical skills, attention to detail, and the ability to work collaboratively across departments. Join a dynamic team dedicated to advancing clinical trials and improving patient outcomes. If you are ready to make a significant impact in a fast-paced environment, this opportunity is for you.
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Summarized Purpose
The Clinical Data Strategist (CDS) is accountable for tactical, detailed, high quality, and on-time data review deliverables. The CDS acts as the lead subject matter expert and interdepartmental and client liaison for data review activities with focus on the development of study level analytic tools to detect, investigate, diagnose and mitigate issues and risk, set up and development of functional plans and data review tools.
A Day in the Life:
Job Complexity
Works on issues of diverse and complex scope where variable factors will require in-depth analysis, critical thinking, risk assessment and management, problem solving and determination of correct action.
Job Knowledge
An experienced professional with full understanding of area of specialization. Uses professional concepts and company objectives to resolve complex issues effectively.
Business Relationships
Frequent contacts with internal personnel and outside customer representatives at various management levels concerning operations and requires coordination between functional areas. Creates formal networks with key contacts outside own area of expertise.
Education and Experience
Bachelor's degree or equivalent and relevant formal academic / vocational qualification previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years). Prior experience in clinical monitoring, centralized monitoring, data management, biostatistics or related field in support of clinical trials is preferred. In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, skills and abilities
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Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.