833#Principal Statistical Programmers-RARE DISEASE/Oncology (Remote) at ClinChoice
Remote, Oregon, USA -
Full Time


Start Date

Immediate

Expiry Date

30 Jul, 25

Salary

0.0

Posted On

01 May, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Interpersonal Skills, Data Standards, Computer Science, Biotechnology Industry, Sas Programming, Validation, Study Reports, Statistics, Oncology

Industry

Pharmaceuticals

Description

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds…
ClinChoice is searching for a Principal Statistical Programmer Consultant -Rare Disease/ONCOLOGY to join one of our clients.
ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.

REQUIREMENTS:

Minimum of 10 years of SAS programming in the pharmaceutical or biotechnology industry with a BA/BS in computer science, statistics, math or MA/MS with 8 years of experience;
Expertise in SAS programming language, report generation, and standards for programming and validation;
Therapeutic area- Rare Disease or Oncology
Experience with CDISC data standards required;
Experience as a senior statistical programmer level in a pharmaceutical or CRO working in a FDA regulated environment;
Experience with Clinical Study Reports and NDA submission;
Ability to work on multiple tasks simultaneously and meet project deadlines;
Excellent verbal/written and interpersonal skills required for working successfully in a cross-functional team environment.

Responsibilities

Participate in CRF design, database review, data management plan, data review, data validation procedures, and review of data listings;
Produce data listings, summary tables and graphics for interim and final analyses;
Integrate data across studies within a project. Test, document, review and validate all programs according to department guidelines;
Coordinate data transfer and/or programming standards with CROs and vendors. Validate analysis datasets and TFLs from vendors;
Collaborate with other Biometrics functions for all activities related to analyses of clinical trial data;
Responsible for execution of ad-hoc requests, manuscripts, posters, and presentations.

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