Remote Statistical Programmer III – Clinical Trials (SAS)

Artech LLC.; East Hanover (NJ); Remote; USD 65,000 - 90,000; Full time

Job summary

Artech Information System LLC in Morristown, NJ, seeks a statistical programmer to support Phase II–IV clinical trials. You will develop SAS programs to create analysis datasets, tables, listings and figures, and contribute to protocol validation and study reporting.

Requirements include 1–2 years of analytical experience, 2–5 years SAS experience with clinical trial data, and strong communication skills for cross-functional teams in a remote setting.

Qualifications

• 1–2 years of Analytical experience in pharma or associated field.
• Intermediate Pharma industry SAS experience required, with 2–5 years experience in a medical setting, preferably working with clinical trial data.
• Good understanding of clinical trial practices, procedures and methodologies.
• Good verbal and written communication skills.

Responsibilities

• Provide statistical programming support and validation for analysis datasets, tables, figures and listings for Phase II–IV trials.
• Employ standardized programs where applicable.
• Contribute to planning documents such as protocol, validation plan, and report analysis plan.
• Prepare outputs for clinical study reports and electronic submissions.
• Assist in responding to health authority inquiries for dossiers and submissions.
• Coordinate with biostatistics and clinical research teams to ensure effective communication.

Skills

SAS experience

Clinical trial data

Communication skills

Interpersonal skills

Office tools

HARP knowledge

Education

BA/BS or equivalent

Tools

HARP environment

GSK programming environment

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

Notes - Its a Remote Position in which, the client is looking for someone with Working knowledge of HARP, the GSK programming environment, will be a plus.

Job Description:

• Candidate to provide statistical programming support and validation and help set specifications of analysis datasets, pooled datasets, statistical tables, summaries, figures and listing for Phase II-IV clinical trials.

• Employ standardized programs where applicable.

• Provide input into planning documents such as protocol, validation plan, and report analysis plan.

• Provide outputs for clinical study reports, integrated summaries and electronic submissions.

• Help respond to health authority inquiries for submitted dossiers.

• Establish and maintain sound working relationship and effective communications within biostatistics and statistical reporting and clinical research.

Skills:

• 1-2 years of Analytical experience.

• Intermediate Pharma industry SAS experience required, with 2-5 year s experience in a medical setting, preferably working with clinical trial data.

• Good understanding of clinical trial practices, procedures and methodologies.

• Good verbal and written communication skills.

• Good interpersonal and organizational skills.

• Attention to detail and correctness.

• Working knowledge of office tools.

• Working knowledge of HARP, the GSK programming environment, will be a plus.

Qualifications

• BA/BS or equivalent experience in computer science, mathematics, statistics, life sciences, or related field(s).

Additional Information

Best Regards,

[phone] Ext.4554

Morristown, NJ 07960

By clicking the link above or any third-party link within this posting, you are leaving this site and going to a third-party website where the third-party website's terms and privacy policy apply