SPECTRAFORCE

Analyst, Data Analytics

⭐ - Featured Role | Apply direct with Data Freelance Hub
This role is for an Analyst, Data Analytics in Irvine, CA (Hybrid) for 12 months, offering competitive pay. Requires a Bachelor's degree, 3 years of experience, strong Python skills, and familiarity with clinical trial operations in the medical device industry.
🌎 - Country
United States
πŸ’± - Currency
$ USD
-
πŸ’° - Day rate
320
-
πŸ—“οΈ - Date
April 13, 2026
πŸ•’ - Duration
More than 6 months
-
🏝️ - Location
Hybrid
-
πŸ“„ - Contract
Unknown
-
πŸ”’ - Security
Unknown
-
πŸ“ - Location detailed
Irvine, CA
-
🧠 - Skills detailed
#NumPy #Libraries #Datasets #Python #Data Review #Pandas #Visualization #Monitoring #Programming #Data Analysis #Statistics #Trend Analysis #Data Quality #"ETL (Extract #Transform #Load)" #Forecasting #Strategy
Role description
Position Title: Analyst, Data Analytics Work Location: Irvine, CA (Hybrid) Assignment Duration: 12 Months Position Summary: Perform quantitative analysis using Python (e.g., pandas, NumPy, visualization libraries) to support clinical trial operations such as enrollment, costing, and resourcing, and to develop forecasting and decision-support outputs for key stakeholders (e.g., Clinical Affairs, Regulatory and Medical Affairs, Strategy, Global Supply Chain, Finance). Investigate, assess, and interpret clinical and operational data to support strategic decision-making, including early signal detection related to enrollment trends, protocol adherence, site performance, and data quality, while proposing moderately complex solutions and recommendations. Key Responsibilities: β€’ Perform quantitative analysis using Python (e.g., pandas, NumPy, visualization libraries) to support clinical trial operations such as enrollment, costing, and resourcing, and to develop forecasting and decision-support outputs for key stakeholders (e.g., Clinical Affairs, Regulatory and Medical Affairs, Strategy, Global Supply Chain, Finance). β€’ Investigate, assess, and interpret clinical and operational data to support strategic decision-making, including early signal detection related to enrollment trends, protocol adherence, site performance, and data quality, while proposing moderately complex solutions and recommendations. β€’ Modify, extend, and maintain analysis tools and workflowsβ€”primarily in Pythonβ€”by leveraging existing clinical models (e.g., inventory, case management, headcount, trial enrollment, site activations/deactivations) while applying clinical trial domain knowledge. β€’ Organize, analyze, and create reproducible analyses, reports, dashboards, and data extracts to summarize moderately complex challenges across clinical affairs projects, programs, and initiatives. β€’ Apply statistical methods (e.g., descriptive statistics, trend analysis, basic inferential methods) as appropriate to quantify uncertainty, monitor performance, and support interpretation of clinical and operational signals. β€’ Lead portions of clinical analytics projects in collaboration with cross-functional stakeholders (e.g., Clinical Operations, Biostatistics, vendors, and internal analytics partners). β€’ Identify and propose data-driven process improvements related to clinical affairs operations (e.g., screening efficiency, site start-up, physician training, data review workflows). β€’ Other duties as assigned. Qualification & Experience: β€’ Bachelor's Degree Required β€’ 3 years of previous related experience Required β€’ Experience in a quantitative, analytical, or programming-heavy role Preferred β€’ Experience working in clinical research or clinical trial operations within the medical device industry Preferred β€’ Strong proficiency in Python for data analysis, including developing maintainable scripts and notebooks for clinical and operational datasets β€’ Proven expertise in Excel and PowerPoint and other MS Office Suite applications (Word, Access) β€’ Solid understanding of quantitative and statistical methodologies, with the ability to apply them pragmatically in a clinical operations context β€’ Experience with signal detection, trend monitoring, or anomaly identification in complex datasets preferred β€’ Good written and verbal communication skills and interpersonal relationship skills β€’ Strong problem-solving, organizational, analytical, and critical-thinking skills β€’ Moderate knowledge and understanding of client's policies, procedures, and guidelines relevant to clinical trial data analytics β€’ Strict attention to detail and data quality β€’ Ability to interact professionally with all organizational levels β€’ Ability to manage competing priorities in a fast-paced environment β€’ Ability to work collaboratively in team and cross-functional environments β€’ Ability to build productive internal and external working relationships β€’ Adhere to all company rules and requirements (e.g., Environmental Health & Safety policies) and take appropriate measures to protect people, data, and the environment.