Job detailsData Analyst/Project Support - STL MOKelly Science and Clinical is currently recruiting for a qualified, full-time, temporary to potential permanent Data Analyst/Project Support role. The position is in St. Louis, MO, and the need to fill this position isimmediate.Summary of the Position:The Data Analyst will be part of our growing team and be involved in project management, data review, and data reporting to external collaborators. This role would allow for transition into more project management responsibilities over time as well. The qualified candidate must be a skilled user of Microsoft Excel, be familiar with scientific data analysis, and general data transformations.Responsibilities:
- Coordinates internal resources and third parties/vendors and assists in the execution of projects.
- aids in delivering projects on time, within the scope and budget.
- Assists in defining project scope and objectives with all relevant stakeholders and ensuring protocol feasibility with laboratory workflow and study setup.
- Contributes development of a detailed project plan to monitor and track progress and shares with clients and cross-functional team.
- Helps in managing changes to the project scope, schedule, and costs.
- Manages the relationship with assigned clients and all stakeholders.
- Establishes and maintains relationships with third parties/vendors.
- Creates and maintains comprehensive project documentation.
- Tracks project performance, esp., successful completion of short and long-term goals
- Helps in developing spreadsheets, diagrams, and process maps to document needs.
- Maintain compliance with all company policies, SOPs, GLP, ICH- GCP, regulatory, and project specific requirements.
- Contributes to the day-to-day management of project finances including performing financial analyses, updates, and required follow-up with functional leads when necessary.
- Compiles project reports and status updates
- Prepares data files to be shared externally and ensuring data quality and conformance to diverse standards/specifications.
- Assists the clinical and regulatory affairs teams with data integrity review, collection, and reporting, and clinical studies performed in connection with external investigators and/or pharmaceutical company clients.
- Review data for deficiencies or errors, correct and trouble shoot any incompatibilities and review data output.
- Demonstrated ability to follow data transfer specifications or data transfer agreements.
- Communication of data to 3rd parties
- Reviewing, editing, and implementing data reporting specifications
- Resolving data queries from clients
Qualifications/Education/Skills:
- Bachelor's degree in biomedical sciences (Biology, Analytical or Clinical Chemistry, Life Sciences) or related area with demonstrated interest or initiative for Project Management in the clinical research and clinical diagnostics environment.
- Current or prior experience working for a CRO or Sponsor supporting regulated studies is strongly preferred
- 2-3+ years of related experience
- Detail oriented
- Excellent organizational skills
- Excellent verbal and written communication
- Demonstrated agility with ability to work under changing priorities
- Proficiency in Microsoft Excel (pivot tables, data sort and filters, visual basic formulas) and MS office tools. An intermediate level Microsoft Excel assessment with a satisfactory score is required for this role.
Additional Perks to have:
- Knowledge of regulatory studies and quality systems
- Prior work experience in GCP/GLP/CLIA environments
- Experience with laboratory information management systems (LIMS)
- Experience with data manipulation tools such as R/Tableau
- Familiarity with online data transfer and storage solutions such as FTP
Pay: $25-30/hr - possibly higher based on experienceHours: Mon - Fri, 8A - 5P - onsite work setup - no remote optionFor more information or consideration, please contact me directly at ...@kellyscientific.com or at 804-###-####!#GOKELLY9606664