Job Description
job summary:
As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!
location: Telecommute
job type: Contract
salary: $35 - 45 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
- Write and review statistical analysis plans for analytical and clinical validation studies.
- Apply DOE principles, conduct statistical analyses, and clearly communicate interpretations.
- Calculate clinical accuracy metrics (PPA, NPA, PPV, NPV) and deliver analyses to support regulatory filings.
- Generate tables, listings, and figures aligned with study protocols.
- Review and QC statistical outputs from peers, ensuring scientific integrity.
- Write and validate SAS code and macros to support standardized workflows.
- Collaborate in cross-functional study teams, contributing data-driven insights that influence key decisions.
- Partner with colleagues across functions to advance innovative diagnostics.
qualifications:
- BS in Statistics or Biostatistics + 5 years of experience, OR
- MS in Statistics or Biostatistics + 1 year of experience, OR
- PhD in Statistics or Biostatistics.
- SAS programming certification is a plus.
Experience
- Proven experience as a statistician in IVD, medical devices, pharmaceutical, or life sciences settings.
- Strong SAS (BASE, STAT, MACRO, GRAPH) programming Skills.
- Experience analyzing complex data from multiple sources and familiarity with CLSI standards.
- Knowledge of Next-Generation Sequencing (NGS) is a plus.
Knowledge, Skills & Abilities - Solid understanding of statistical theory, experimental design, and clinical trial methodologies.
- Proficiency with linear and non-linear modeling, mixed models, categorical and nonparametric methods, bootstrapping, multiple imputations, and sample size calculations.
- Ability to manage multiple projects in a fast-paced environment.
- Skill in translating scientific questions into practical, data-analytic solutions.
- Excellent written and verbal communication skills - able to simplify complex ideas and build strong partnerships.
- Flexibility to work across multiple time zones when needed.
skills: SAS, SAS Macro, SAS/GRAPH, SAS/STAT
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.
Job Tags
Hourly pay, Contract work, Temporary work, Work experience placement, Remote work