Senior Associate Statistical Programmer

This role will be required to be on-site at least 1-2 days per week.

ROLE SUMMARY

• A productive, hands-on programmer who applies technical knowledge and practical experience to deliver statistical programming deliverables to support assets and study teams with limited supervision early in role and independently later in role.

• Ensures excellence in the programming of analysis ready datasets, tables, listings, and figures for which they are responsible.

• Ensures adherence to high quality programming standards in their daily work.

ROLE RESPONSIBILITIES

• Accountable for the quality and timely delivery of datasets and displays required for their clinical study reports as well as other asset level deliverables they may be programming.

• Ensures appropriate documentation and QC across the lifespan of the study for all of their programming deliverables.

• Exhibits routine and occasionally complex problem-solving skills, seeking direction when appropriate.

• Works with statisticians and programming leads to ensure clear specifications for their programmed deliverables are in place.

• Will be knowledgeable in core safety standards as well as TA standards pertinent to their project, may aid in development of standards necessary for their study.

• May contribute to department level initiatives.

QUALIFICATIONS

• Bachelor or Master (preferred) Degree in Statistics, Biological Sciences, IT, or related field.

• At least 3 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.

• Statistical Programming and SAS hand-on experience.

• Clinical trials expertise with an understanding of data operations required for the reporting of clinical trial data.

• Good understanding of ICH and regulatory guidelines.

• Working knowledge of clinical data and relevant data standards.

• Strong written and oral communication skills, and project management skills.

• Proven ability to operate with limited oversight.

• Knowledge of at least 1 Therapeutic Area.

• Proven ability to manage delivery under tight timelines.

• CDISC experience desirable.

• Remote based may be considered.

Other Job Details:

• All applicants must have the relevant authorisation to live and work in the UK or Canada

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Purpose 

Breakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.  

Digital Transformation Strategy

One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.

Flexibility  

We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the conversation!  

Equal Employment Opportunity 

We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.

DisAbility Confident

We are proud to be a Disability Confident Employer and we encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments necessary to support your application and future career. Our mission is unleashing the power of our people, especially those with unique superpowers. Your journey with Pfizer starts here!

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