Job Title: Clinical Application Specialist III

Pay rate: $90 per hour

Duration: 12 months

W2 contract only (No C2C)

Location- REMOTE (Company location- South San Francisco, CA)

Description

Experience and Skills Required:

Clinical Trial Data Analysis: 8 years of experience using SAS, preferably in a UNIX environment. Familiarity with UNIX commands and environment is essential.

CDISC Standards & ADaM Programming: Deep knowledge and solid experience in ADaM programming, with Oncology Therapeutic Area (TA) experience preferred.

Learning and Interpretation: Ability to quickly learn internal macros and processes, and interpret Pinnacle 21 results.

ISS/ISE ADaM Programming: Experience in supporting Integrated Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE) ADaM programming and submissions is a plus.

Team Collaboration: Team player with excellent communication skills and experience working with statisticians, programmers, and data management personnel.

Notes from the Manager:

Length of the Assignment:

Working Hours and Days: 9 AM – 5 PM, Monday to Friday. Preferred time zones are Pacific Time Zone or Central Standard Time (CST).

Top 5 Skills/Requirements:

1. SAS Programming: Familiar with SAS language modules, e.g., SAS MACRO, BASE, SGPLOT, SQL.
2. Macro Programming: Proficiency in writing and comprehending existing macros.
3. Dataset Derivation: Knowledgeable about derived dataset derivation and specification files.
4. Technical Competence & Communication: High degree of technical competence and strong oral and written communication skills.
5. Industry Experience: Experience in the pharmaceutical or related industry, particularly with clinical trials.

Experience, Education, and/or Certification Required:

MS in Statistics, Computer Science, or a related field with 6 years of relevant experience.

BS in Statistics, Math, Computer Science, or a STEM-related field with relevant experience.

Nice to Have:

SAS certification is desirable but not required.

Work Environment:

The role involves working in a group setting.

Testing Requirements:

No testing is required for this role.

Remote Work Opportunities:

This position offers the ability to work remotely on a regular basis.

Additional Environment Details:

The role involves working with SAS Enterprise Guide (EG) and UNIX environment, ASPEN, and SAS Studio.

Successful Background Experience:

Candidates with pharmaceutical or related industry experience, particularly in clinical trials and CROs, are likely to be successful in this role.

*** If this position may be interested to you, please email me back at somp767@kellyservices.com (with your most up to date resume in word format) and advise the best time and number at which you can be reached****