A research-driven biopharmaceutical powerhouse focused on developing treatments for complex, hard-to-cure diseases. This esteemed company has brought 32 groundbreaking products to market, making a significant global impact. If you're ready to make your mark in the field and contribute to the future of innovative therapies, this is the opportunity for you!
location: Telecommute
job type: Contract
salary: $50 - 57 per hour
work hours: 9 to 5
education: Doctorate
responsibilities:
- Contribute to design, analysis and reporting of clinical trials or other scientific research studies.
- Assist with development of protocols and/or statistical analysis plans with details for programming implementation.
- Work under supervision to implement sound statistical methodology in scientific investigations.
- Identify and report data issues or violations of study assumptions.
- Provide programming specifications for derived variables and analysis datasets.
- Collaborate with Data Science in preparing for database lock.
- Perform statistical analyses as per the analysis plan.
- Collaborate with Statistical Programming to ensure the delivery of high-quality outputs according to agreed-upon timelines.
- Evaluate appropriateness of available software for planned analyses and assess needs for potential development of novel statistical methodology.
- Develop strategy for data presentation and inference.
- Ensure appropriate interpretation of statistical deliverables in collaboration with other functions.
- Ensure accuracy and internal consistency of reports, including tables, listings, and figures.
- Ensure the accuracy of the statistical component of scientific reports with high quality.
- Work collaboratively with cross-functional teams.
- Clearly explain statistical concepts to non-statisticians.
- Provide responses to questions and pursue analyses suggested by data.
- Support communications between assigned product team(s) and functional management.
- Build/drive cross-functional relationships and collaboration.
qualifications:
Required Qualifications
- PhD in Statistics with 1-3 years of experience or MS in statistics with 5-7 years of experience
- Strong statistical methodology knowledge
- Prior experience in Pharma industry reviewing SAP/protocol/CSR/database cleaning etc.
- Experience in Phase I is a plus
skills: CSR, Six Sigma Methodologies, Clinical Study Report (CSR)
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.
