Sr. Biostatistician needed for Remote Job longterm Contract!!!

Sr. Biostatistician needed for Remote Job longterm Contract!!!

Posted 5 days ago by 1753582523

Negotiable
Outside
Remote
USA

Summary: The role of Sr. Biostatistician involves leading statistical aspects of clinical studies, ensuring compliance with industry standards, and mentoring junior biostatisticians. The position is remote and requires candidates to work in the EST time zone. The contract duration is for 6+ months, and only independent contractors are eligible to apply. Candidates must have significant experience in statistical programming and analysis.

Key Responsibilities:

  • Lead statistical aspects of clinical studies from design to final reporting
  • Review and approve programming deliverables (ADaM datasets, tables, listings, and figures)
  • Ensure compliance with industry standards (CDISC, ICH, FDA/EMA guidelines)
  • Draft SAP/shell independently
  • Mentor junior biostatisticians and support team development
  • Work in detail and review the TLF
  • Excellent communication and leadership skills with cross-functional collaboration experience

Key Skills:

  • At least 8 years of experience
  • Statistical Programming II experience
  • Proven expertise in SAS and/or R for statistical analysis
  • Excellent communication and leadership skills
  • Experience in mentoring junior biostatisticians
  • Ability to ensure compliance with industry standards

Salary (Rate): undetermined

City: undetermined

Country: USA

Working Arrangements: remote

IR35 Status: outside IR35

Seniority Level: undetermined

Industry: Other

Detailed Description From Employer:

Dear,

Hope you are doing well.

Send resumes along with expected bill rates on W2( NO Benefits) or Independent contractors only apply and share to

Note : NO 3rd party candidates, or H1's/EAD's/OPT's please.

Role : Sr. Biostatistician

Location:Remote

Duration : 6+ months contract

EST time zone- candidate need to work in EST time

Skills:

  1. At least 8years of experience
  2. In Addition to the above Statistical Programming II experience
  3. Lead statistical aspects of clinical studies from design to final reporting
  4. Review and approve programming deliverables (ADaM datasets, tables, listings, and figures)
  5. Proven expertise in SAS and/or R for statistical analysis
  6. Mentor junior biostatisticians and support team development
  7. Ensure compliance with industry standards (CDISC, ICH, FDA/EMA guidelines)
  8. Draft SAP/shell independently.
  9. Work in detail and able to review the TLF;
  10. Excellent communication and leadership skills with cross-functional collaboration experience

Manjunath

Staffing Manager

Nam Info Inc

Ph: / Email:

Website:

Address: 2525 US Highway 130, Bldg D, Suite2 Cranbury, NJ-08512

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