#748-Senior Statistical Programmer Consultant -Remote in Mexico Mexico

ClinChoice Inc.; Mississippi; Remote; USD 80,000 - 120,000; Full time

Job summary

A forward-thinking company is seeking a Senior Statistical Programmer Consultant to join their team. This role offers a unique opportunity to work directly with a single sponsor while benefiting from the security and career growth provided by a global CRO. You will be responsible for data management, producing analytical reports, and collaborating with cross-functional teams to ensure high-quality delivery of clinical trial data. If you have extensive experience in SAS programming and a passion for contributing to innovative drug development, this position is perfect for you. Join a diverse and inclusive environment where your skills will make a significant impact.

Qualifications

• 10+ years of SAS programming experience in pharmaceuticals or biotechnology.
• Expertise in data management and clinical trial data analysis.

Responsibilities

• Participate in CRF design, database review, and data validation procedures.
• Produce data listings and summary tables for analyses.

Skills

SAS Programming

Data Management

Clinical Study Reports

Cross-functional Team Collaboration

Report Generation

Education

BA/BS in Computer Science

MA/MS in Statistics or Math

Tools

CDISC Data Standards

Job 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 Senior Statistical Programmer Consultant 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.

Main Job Tasks and Responsibilities:

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

Requirements:

1. 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;
2. Expertise in SAS programming language, report generation, and standards for programming and validation;
3. Experience with CDISC data standards required;
4. Experience as a senior statistical programmer level in a pharmaceutical or CRO working in a FDA regulated environment;
5. Experience with Clinical Study Reports and NDA submission;
6. Ability to work on multiple tasks simultaneously and meet project deadlines;
7. Excellent verbal/written and interpersonal skills required for working successfully in a cross-functional team environment.

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

About ClinChoice

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.

Our Company Ethos

Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.

ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.

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