Principal statistical programmer sponsor dedicated, emea Work, Jobs in Reading, Eng (with Salaries)

Principal Statistical Programmer - Sponsor Dedicated, EMEA
Fortrea —Maidenhead
- Full-time
- English
- Mentoring
Senior or Principal Statistical Programmer - ONCOLOGY - Sponsor dedicated
Fortrea —Maidenhead
- Full-time
- English
- Quality control
- Organisational skills
Lead Statistical Programmer - Sponsor Dedicated
Fortrea —Maidenhead
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- English
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Data Team Lead, EMEA
IQVIA —Reading
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- Bachelor's degree
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Spin Master Ltd —Marlow
- Full-time
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- Budgeting
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Sr. Principal Scientist, Advisor, Sr. Advisor of Global Regulatory Affairs Chemistry, Manufacturing & Controls and Devices-EMEA
Eli Lilly —Bracknell
- Full-time
- Doctoral degree
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Qualcomm —Farnborough
- Doctoral degree
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Vantive —Newbury
- Remote
- English
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Extreme Networks —Reading
- Full-time
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- English
- Bachelor's degree
Quick apply
5d
Snr Data Team Lead, EMEA
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Continuous improvement
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6d
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NETGEAR —Bracknell
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Quick apply
8d
Graduate Devops Engineer, AWS
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Support Technician (EMEA Helpdesk)
Utelogy —Basingstoke
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Quick apply
Activation Specialist, EMEA
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Utelogy —Basingstoke
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Quick apply
14d
Sr. Director, AS Technology & Commercial Acceleration - EMEA
TD Synnex —Basingstoke
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Invesco —Henley on Thames
- Full-time
- Hybrid work
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Account Executive 2 - EMEA
Egnyte —Reading
- Full-time
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- Salesforce
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Cloud Intelligence Business Development Manager - EMEA, AWS Cloud Intelligence
AWS EMEA SARL (UK Branch) —Thames Valley
- Full-time
- Sales
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- Bachelor's degree

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principal statistical programmer sponsor dedicated, emea jobs near reading, eng

Principal Statistical Programmer - Sponsor Dedicated, EMEA

Fortrea -
Maidenhead

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Job details

Full-time

Qualifications

Clinical research
Stakeholder collaboration
XML
SAS
Stakeholder liaison
Mentoring junior staff
Mathematics
Internal department liaison
English
Mentoring
Multidisciplinary collaboration
Pharmaceutical industry setting experience

Full job description

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

As a Principal Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex projects for a renowned, innovative and global top pharmaceutical company.

You will be involved in liaising with the entire study team as needed, including Clinical, Medical Writing, Safety and Biometrics. It is a great opportunity to see more how this works from a Big Pharma perspective, whilst still being part of a global CRO with opportunity for future career growth.

This position allows you to participate in the development of innovative new benchmark drugs for a wide variety of therapeutic areas.

You can be 100% home-based in EMEA or you can work from our local office in your home country.
Your Responsibilities:
Plan, execute and oversee all programming activities on a study, including but not limited to: resource estimation, working within budget, meeting timelines, maximizing quality, interaction with other departments, etc.

Oversee SDTM, ADaM and TLF development, perform Senior Review of outputs.

Liaise with other Sponsor departments for additional programming needs, as required to support publications, medical writing and additional development needs and analyses.

Support/oversee submission activities (especially in late phase team).

Ensure all activities are conducted efficiently, with appropriate set-up of needed tools and macros, prioritizing quality at all times.

Mentor less-experienced team members in best practices around SDTMs, ADaMs and TFLs while ensuring adherence to department standards and processes.

Your Profile:
Ideally, a degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc.

In lieu of the above: professional experience in statistical programming within clinical trials in a biotech, CRO or pharmaceutical company.
Solid experience with complex clinical trials (minimum 5 years) and the corresponding data sets content (safety and efficacy) and endpoints.
Ideally you will have knowledge in all aspects of clinical trials, from initial study set-up to study completion, with an understanding of the roles and responsibilities of all related disciplines, e.g. Biostatistics and Clinical Data Management.

Expert knowledge of base SAS, SAS macros, SAS/STAT and in debugging SAS programs.

Broad knowledge of all CDISC requirements related to SDTM and ADaM, including define.xml, Reviewer's Guides and submission standards.

An autonomous, collaborative work style, a curious mind and a keen attention to detail.

Fluency in English – both verbal and written – is a must.
Learn more about our EEO & Accommodations request here .

Apply Now

Refine Your Search

principal statistical programmer sponsor dedicated, emea jobs in reading, eng

Principal Statistical Programmer - Sponsor Dedicated, EMEA

Senior or Principal Statistical Programmer - ONCOLOGY - Sponsor dedicated

Lead Statistical Programmer - Sponsor Dedicated

Data Team Lead, EMEA

Senior Director, Information Technology EMEA

Sr. Principal Scientist, Advisor, Sr. Advisor of Global Regulatory Affairs Chemistry, Manufacturing & Controls and Devices-EMEA

Senior Director/Director EMEA HR Business Partner/Leader - Qualcomm, UK or Germany

Senior Learning Specialist - EMEA

Integrated Campaigns and Programs Manager – EMEA

Snr Data Team Lead, EMEA

Senior Broadcast Systems Engineer, EMEA

Graduate Devops Engineer, AWS

Support Technician (EMEA Helpdesk)

Activation Specialist, EMEA

Project Engineer (EMEA)

Sr. Director, AS Technology & Commercial Acceleration - EMEA

EMEA Engineering Graduate Program

EMEA AML Officer

Account Executive 2 - EMEA

Cloud Intelligence Business Development Manager - EMEA, AWS Cloud Intelligence

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