FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in statistical analysis and biostatistics, particularly in the context of Phase I-IV clinical trials. Proficient in SAS and Microsoft Office tools, with strong communication skills and the ability to manage multiple tasks effectively under tight deadlines.
Highest-signal resume keywords
PhD In Statistics Or BiostatisticsSAS Proficiency Including BASE And STATStatistical Methods For Phase I-IV Clinical TrialsBiostatistical Experience In Clinical TrialsExcellent Written And Oral Communication Skills
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Statistical AnalysisBiostatisticsStatistical MethodsClinical Trial Data AnalysisTechnical Writing
Soft Skills
Detail OrientationTime Management
Tools & Technologies
SASMicrosoft WordMicrosoft Excel
Industry Keywords
Clinical TrialsHealth ResearchPhase I-IV Trials
About the role
Key responsibilities & impact- Perform analysis of clinical trial data
- Provide statistical input into reporting of clinical trial results
- Work largely independently with minimal oversight from the Director or Manager of Biostatistics, or Senior Biostatistician
- Apply statistical methods to Phase I-IV clinical trials
- Manage multiple tasks under tight timelines
Requirements
What you’ll need- PhD degree in Statistics, Biostatistics, or related field with relevant academic experience OR a Master’s degree in Statistics or Biostatistics or a related field and 3 years of biostatistical experience in the clinical trials or health research environment OR a Bachelor’s degree in Statistics, Biostatistics or a related field and 5 years of biostatistical experience in a clinical research organization in a hands-on technical position with a demonstrated ability to perform the duties above
- Excellent written and oral communication skills including grammatical/technical writing skills
- Familiarity with moderately complex statistical methods that apply to Phase I-IV clinical trials
- SAS proficiency including BASE and STAT; GRAPH preferred
- Proficiency in Microsoft Word and Excel
- Strong level of detail orientation
- Ability to work on multiple tasks under tight timelines
Benefits
Comp & perks- Remote working
- Flexible time off
- Paid holidays
- Medical insurance
- Tuition reimbursement
- Retirement plans
- Applicable bonus
