Programmer sponsor Work, Jobs in Camberley, Eng (with Salaries)

Senior Statistical Programmer - Sponsor Dedicated
Fortrea —Maidenhead
- Full-time
- Remote
- English
- Quality control
- Organisational skills
Senior or Principal Statistical Programmer - ONCOLOGY - Sponsor dedicated
Fortrea —Maidenhead
- Full-time
- English
- Quality control
- Organisational skills
Lead Statistical Programmer - Sponsor Dedicated
Fortrea —Maidenhead
- Full-time
- English
- Mentoring
Sr. Clinical Data Manager (Netherlands, United Kingdom)
Allucent —Bracknell
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Bachelor's degree
- Training & development
- Flexible schedule
- Referral programme
Quick apply
Principal Statistical Programmer - Sponsor Dedicated, EMEA
Fortrea —Maidenhead
- Full-time
- English
- Mentoring
Senior Technical Designer - Medidata RAVE Certification required
Fortrea —Maidenhead
- Full-time
- Remote
- English
- Databases
- Quality control
Senior Clinical Data Manager - sponsor dedicated - oncology
Fortrea —Maidenhead
- Full-time
- Remote
- Presentation skills
- Mentoring
- Leadership
DM/STDM Programmer
IQVIA —Reading
- Full-time
- Remote
- English
- Communication skills
- Work from home
4d

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Senior Clinical Data Manager - sponsor dedicated - oncology
Fortrea —Maidenhead
8 years of combined early or late-stage DM experience with minimum 2 years of direct sponsor management and at least 2 years technical mentoring experience.
Senior or Principal Statistical Programmer - ONCOLOGY - Sponsor dedicated
Fortrea —Maidenhead
You can be 100% home-based , or if you prefer, work from one of our local offices in your home country. Perform programming activities for oncology clinical…

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Senior Statistical Programmer - Sponsor Dedicated

Fortrea -
Maidenhead

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Job details

Full-time

Qualifications

Clinical research
XML
SAS
Mathematics
English
Quality control
Organisational skills
Pharmaceutical industry setting experience
Debugging

Full job description

This role is for upcoming future opportunities that may arise at Fortrea.

As a Senior Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex clinical trials (phases I-III) for renowned, innovative and global top pharmaceutical companies. Oftentimes you will have the opportunity to lead studies through various phases of the clinical development plan and support submissions, regulatory questions, publications as well as ad hoc and post hoc requests.

In this role, you will develop and validate SAS programs for data presentations and analyses and provide programming support to your multidisciplinary global project team. This position allows you to participate in the development of innovative new benchmark drugs for a wide variety of therapeutic areas. Your expertise and your work as a statistical programmer have a direct impact on improving the health and lives of thousands of patients around the globe every day.

You can be 100% home-based or if you prefer, you can work from our local office in your home country.

Your Responsibilities:

Review SAPs and TFL shells from a programming perspective.
Advise on the development of complex TFL shells from a programming perspective.
Develop and/or lead the development of complex specifications for SDTMs and ADaM datasets.
Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform quality control of SDTM, ADaMs and TFLs.
Produce / define XML / PDFs, Analysis Results Metadata (ARM), aCRFs and Reviewers Guides to support SDTMs and ADaMs.
Respond to QA and client audits and support qualification audits.
Identify and propose innovative ways to improve the efficiency, quality and productivity of our clinical statistical programming business.
Maintain awareness of industry standards, global regulatory requirements, internal guidelines and Standard Operating Procedures (SOPs).

Your Profile:

Degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc.
In lieu of the above: an equivalent completed vocational training and / or equivalent professional experience in statistical programming for clinical trials.
Solid professional experience as a statistical programmer within a biotech, CRO or pharmaceutical company.
Demonstrated knowledge of base SAS, SAS macros, SAS/STAT; demonstrated ability to debug SAS programs.
Proven professional experience with SDTMs, ADaM datasets (safety and efficacy) and TFLs.
Solid knowledge of CDISC standards.
Submission experience is ideal.
Strong organizational skills, an autonomous and collaborative work style, a curious mind and a keen attention to detail.
Business fluency in English – both spoken and written – is a must.

Learn more about our EEO & Accommodations request here .

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Refine Your Search

programmer sponsor jobs in camberley, eng

Senior Statistical Programmer - Sponsor Dedicated

Senior or Principal Statistical Programmer - ONCOLOGY - Sponsor dedicated

Lead Statistical Programmer - Sponsor Dedicated

Sr. Clinical Data Manager (Netherlands, United Kingdom)

Principal Statistical Programmer - Sponsor Dedicated, EMEA

Senior Technical Designer - Medidata RAVE Certification required

Senior Clinical Data Manager - sponsor dedicated - oncology

DM/STDM Programmer

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This role is for upcoming future opportunities that may arise at Fortrea.

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