Data manager Work, Jobs in Bracknell (with Salaries)

Lead Statistical Programmer - Sponsor Dedicated
Fortrea —Maidenhead
- Full-time
- English
- Mentoring
Senior Director Data & Innovation
Universal Music Group —London
- Full-time
- Computer Science
- Master's degree
- Bachelor's degree
Group Leader - Cancer Health Data Sciences
ICR —Sutton
- £66,092 a year
- Full-time
- Doctoral degree
- Research
- Analysis skills
Research Group Leader, ICR Clinical Trials and Statistics Unit (ICR-CTSU)
ICR —London
- £66,092 - £86,908 a year
- Doctoral degree
- Master's degree
- Mentoring
Lead Data Engineer
Ceox —Guildford
- Full-time
- Hybrid work
- Azure
- AI
- Leadership
Quick apply
Business Analyst / Data Change Manager
KBR —Leatherhead
- Full-time
- Agile
3h

Discover related jobs

Based on your search for data manager jobs.

Administrator
Eteach Group —Bracknell
Excellent town centre location with on-site parking. Free access to an on-site gym. You will be part of a friendly and supportive team where you will develop…
£25,000 a year
Home Support Administrator
Greensleeves Care —Old Windsor
Demonstrable experience of undertaking general administration duties within a busy environment. Promoting a warm and welcoming environment for residents,…
Up to £32,956.56 a year
Quick apply
1h

I want to receive the latest job alerts for data manager in bracknell

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Lead Statistical Programmer - Sponsor Dedicated

Fortrea -
Maidenhead

Apply Now

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

As a Lead 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.

You can be 100% home-based in EMEA or, if you prefer, 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 datasets’ content (safety and efficacy) and endpoints.
Previous Lead experience preferred.
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

data manager jobs in bracknell

Lead Statistical Programmer - Sponsor Dedicated

Senior Director Data & Innovation

Group Leader - Cancer Health Data Sciences

Research Group Leader, ICR Clinical Trials and Statistics Unit (ICR-CTSU)

Lead Data Engineer

Business Analyst / Data Change Manager

Discover related jobs

I want to receive the latest job alerts for data manager in bracknell

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected