Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Summarized Purpose
The Clinical Data Strategist (CDS) is responsible for tactical, detailed, high-quality, and timely data review deliverables. The CDS serves as the lead subject matter expert and liaison between departments and clients for data review activities, focusing on developing study-level analytic tools to detect, investigate, diagnose, and mitigate issues and risks, as well as setting up and developing functional plans and data review tools.
A Day in the Life:
* Independently lead the development and implementation of results, including data collection and review tools, centralized statistical monitoring tools, and data validation manuals.
* Ensure data reviews are completed on time, including complex analyses or in-depth root cause analyses to connect signals to risks. Lead the development of high-quality reports.
* Lead data review meetings, reviewing trends, outliers, and high-risk sites.
* Mentor junior staff on all tasks within a study and delegate appropriate data reviews based on experience.
* Assist with administrative oversight for assigned projects.
* Communicate with management regarding all activities within their studies.
* Investigate and contribute to the development of innovative technologies to support clinical delivery.
Job Complexity
Handle issues of diverse and complex scope requiring in-depth analysis, critical thinking, risk assessment and management, problem-solving, and appropriate action determination.
Job Knowledge
Possess full understanding of their specialization, applying professional concepts and company objectives to resolve complex issues effectively.
Business Relationships
Maintain frequent contact with internal personnel and external clients at various management levels, requiring coordination across functions and creating networks outside their expertise.
Education and Experience
Bachelor's degree or equivalent plus relevant experience (comparable to 8+ years). Prior experience in clinical monitoring, centralized monitoring, data management, biostatistics, or related fields supporting clinical trials is preferred. An equivalent combination of education, training, and experience may also be considered.
Knowledge, Skills, and Abilities
* Ability to apply knowledge effectively while adhering to guidelines, SOPs, and client expectations.
* Strong attention to detail, organization, and multitasking skills.
* Excellent analytical and problem-solving skills, with sound judgment.
* Leadership ability to motivate and coordinate teams, including mentoring.
* Maintain confidentiality of clinical and proprietary data.
* Strong interpersonal skills, flexibility, and adaptability.
* Effective communication skills in English, both oral and written.
* Proficiency in MS Office and ability to learn new systems.
* Skill in extracting and analyzing study data from documentation and systems.
* Knowledge of resource management, planning, and project management principles.
* Experience acting as a subject matter expert and project leader, including delegation and prioritization.
Apply today! http://jobs.thermofisher.com
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, disability, or other protected statuses.
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