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Clinical Data & Reporting Analyst
Company | ICON Strategic Solutions |
Address | United States |
Employment type | FULL_TIME |
Salary | |
Category | Biotechnology Research,Pharmaceutical Manufacturing |
Expires | 2023-07-15 |
Posted at | 10 months ago |
Responsibilities:
- Programs metrics and reports in a data visualization tool/analyst software (e.g., Power BI, Spotfire)
- Coordinates with Clinical Data Managers and Clinical Data Scientists regarding timelines and deliverables to ensure all reports are working as expected
- Ability to independently develop innovative and complex reports to support activities including, but not limited to, data review and surveillance
- Trains Clinical Data Managers and Clinical Data Scientists on how to generate output (e.g., data review tool, metrics)
- Mentors less proficient Clinical Data Analysts as appropriate
- Develops and maintains the Analytics and Reporting Global Library to ensure consistency across programs and studies and concordance with the EDC Global Library
- May contribute to the development, review and implementation of SOPs, templates and processes and other departmental and/or cross functional initiatives
- Works with Clinical Data Manager, Biomarker Data Specialist, Medical Monitor, and Protocol Lead (and other study team members as appropriate) to develop new or improve existing data review tools
- Evaluate processes and applications for improvements; participate in working groups to develop and implement new processes and applications
Qualifications:
- Familiarity with GCP, ICH and FDA requirements as they apply to clinical data
- Experience with programming languages preferred (e.g., SQL, Python)
- Knowledge of and experience with clinical databases, electronic data capture systems, quality control processes and auditing procedures
- 3-7 years of experience with Analyst software (e.g., Spotfire, Power BI, Tableau), preferably in the pharmaceutical or biotechnology industry
- Excellent written and oral communication skills
- Technical expertise in database and report development
- Regular interaction with Regional Clinical Trial Operations and Medical Management groups
- Regular interaction with other groups within Clinical Data Management, including Clinical Data Programmers, EDC Programmers, and Data Scientists
- Strong critical thinking skills
- Strong well-rounded technical skills (EDC systems, MS Word, Excel, PowerPoint)
Education
- BA/BS in relevant field
Why ICON?
Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
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