Biostatiscian Level-III

Artech Information System LLC; Raritan (NJ); On-site; USD 80,000 - 110,000; Full time

Job summary

A leading IT staffing company is seeking a Statistician to provide statistical input for clinical studies and assist in trial planning and analysis. The ideal candidate will have a Master's degree in Statistics or a related field, along with 2+ years of experience or a PhD, and familiarity with SAS programming. Responsibilities include statistical support for study design, analysis, and report preparation. Strong communication skills and the ability to work independently are essential in this role.

Qualifications

• Masters degree in Statistics or related field and 2 years experience or PhD.
• Basic knowledge of SAS programming and other statistical software.
• Demonstrated written and oral communication skills.

Responsibilities

• Provides primary statistical input for clinical study design.
• Provides analysis planning for clinical studies.
• Provides statistical input to clinical study reports.
• Assists in clinical development planning for new drug indications.
• Provides statistical support across related disciplines.

Skills

SAS programming

Statistical analysis

Communication skills

Independent work

Education

Masters degree in Statistics or related field

PhD in Statistics or related field

Tools

S-Plus

PASS

Job description

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.

Job Description

Statistician working on trial planning and analysis activities with review. Assists project statistician in preparing development programs for new drug indications.

PRINCIPAL RESPONSIBILITIES

• Provides primary statistical input for clinical study design.
• Provides analysis planning for clinical studies.
• Provides statistical input to clinical study reports.
• Assists in clinical development planning for new drug indications.
• Provides statistical support to other disciplines related to clinical statistics.
• Complies with department SOPs and regulatory guidance.

RESPONSIBILITY FOR OTHERS (If applicable)

Describe the nature of supervision exercised over others by this position.

PRINCIPAL RELATIONSHIPS

Describe the primary working relationships (internal & external) and primary interfaces.

1. Biostatistics staff; Clinical Teams and associated working groups
2. Contacts Inside the Company: Therapeutic area scientific staff; SAS Programming; Clinical data management; Clinical Trials Management; Regulatory Affairs; Clinical Communications; Clinical Pharmacology; Medical Writing, Quality Management
3. Contacts Outside the Company: CRO staff; Regulatory Agencies; External Trial Committees

Qualifications

EDUCATION AND EXPERIENCE REQUIREMENTS:

1. Describe the minimum knowledge, skill and ability requirements for the position. Include any degrees or certifications which are required and/or desirable.
2. Masters degree in Statistics or related field +2 years experience or PhD in Statistics or related field.
3. Basic knowledge of SAS programming and at least some other significant statistical software (e.g., S-Plus, PASS). Demonstrated written and oral communication skills. Ability to work independently.

Additional Information

Technical Recruiter (Clinical/Scientific)

Artech Information Systems LLC

360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960

Office: 973.967.3348 | Fax: [phone]

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