This is an incredible opportunity to join a high-impact team of Data Scientists and Engineers dedicated to unleashing the full potential of clinical data assets. You will act as a vital bridge between complex technical datasets and executive decision-making, utilizing advanced analytics to ensure protocol compliance and patient safety across major therapeutic areas like Oncology and Neurology. Based out of a state-of-the-art global research facility known for its commitment to patient-centric innovation and cutting-edge pharmaceutical development, this role offers a dynamic environment where your storytelling and analytical skills directly influence the success of Phase II and III clinical trials.
You will step into a fast-paced, matrixed organization that prioritizes data visibility through sophisticated dashboards and Risk-Based Quality Management (RBQM) activities. As a key consultant for cross-functional stakeholders, you will help decrease current workloads by managing a robust portfolio of studies, translating raw data into actionable business requirements. With a strong potential for conversion and a culture that fosters entrepreneurial thinking, this role is perfect for a professional who thrives on variety and wants to be at the forefront of the digital transformation in clinical research.
location: Telecommute
job type: Contract
salary: $70.00 - 78.21 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
- Study Management: Manage and execute the analytical needs for a portfolio of 13-15 clinical trials simultaneously, ensuring therapeutic alignment and data integrity.
- Stakeholder Consultancy: Partner with cross-functional teams to gather user requirements, translating complex analytical findings into layman's terms for business stakeholders.
- RBQM Implementation: Support the creation of Risk-Based Quality Management deliverables, including Key Risk Indicators (KRIs) and Quality Tolerance Limits (QTLs).
- Advanced Visualization: Design and deploy high-fidelity dashboards and visual analytics to enable real-time data review and study-specific reporting.
- Algorithm Development: Develop prototypes, test methods, and algorithms using R or Python to provide insights into clinical development processes.
- Regulatory Compliance: Ensure all analytical work products adhere to GCP, ICH Guidelines, and federal regulations throughout the trial lifecycle.
- Process Innovation: Identify use cases for Machine Learning (ML) and Artificial Intelligence (AI) to drive innovation in data-driven insights.
qualifications:
Required Skills
- Bachelor's degree in Statistics, Analytics, Bioinformatics, Data Science, or a related field.
- Minimum of 3 years of analytics-related experience specifically within clinical research and the pharmaceutical industry (non-academic).
- Proven proficiency in R programming for statistical analysis.
- Expert-level experience with data visualization tools such as Spotfire, Tableau, or Power BI.
- Direct experience with Phase II and III clinical trials and clinical data datasets.
- Experience performing Risk-Based Quality Management (RBQM) or Risk-Based Monitoring (RBM) activities.
- Strong background in stakeholder management and gathering technical requirements in a matrixed organization.
- Master's degree in a quantitative or scientific field.
- Advanced proficiency in Python or other statistical packages.
- Working knowledge of Machine Learning (ML) and Artificial Intelligence (AI) applications.
- Familiarity with Phase I and IV clinical trial processes.
- Demonstrated leadership competencies and ability to manage multiple high-priority projects in a fast-paced environment.
skills: Data Analysis, R Language
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
