Principal / Associate Director – Statistical Programming

Location:
Barcelona, Catalonia, Spain
Salary:
Negotiable
Type:
Permanent
Main Industry:
Search Health, Nursing & Social Services Jobs
Advertiser:
SEC Recruitment Ltd
Job ID:
131828102
Posted On:
23 April 2025

Principal/Associate Director, Statistical Programming – Barcelona, Spain

Location: Barcelona, Spain (On-Site Only)
Start Date: Immediate start
Position Type: Permanent, Full-Time

A leading global biopharmaceutical organization is currently seeking a Principal or Associate Director-level Statistical Programmer to join its growing team based in Barcelona. This is an on-site, permanent position, available for an immediate start, focused on driving statistical programming strategy and execution across critical clinical development programs.

The role is ideal for a seasoned professional with a minimum of 10 years’ experience in clinical trial programming, strong hands-on technical skills, and a proven ability to lead and manage teams within a regulated environment.

Key Responsibilities:

* Provide technical and strategic leadership for statistical programming deliverables across clinical studies or programs.
* Design, develop, and validate complex SAS programming solutions, ensuring alignment with internal standards and regulatory requirements.
* Lead the implementation and review of datasets and outputs based on CDISC SDTM and ADaM standards to support global regulatory submissions.
* Manage and mentor a team of statistical programmers, supporting both their development and project delivery.
* Oversee planning, resourcing, and quality control of programming activities to ensure timely and accurate deliverables.
* Act as a senior programming representative in cross-functional meetings, collaborating closely with Biostatistics, Data Management, Clinical Operations, and Regulatory teams.

Qualifications:

* At least 10 years of experience in statistical programming within the pharmaceutical, biotechnology, or CRO sector.
* Advanced expertise in SAS programming and a strong command of CDISC standards (SDTM, ADaM).
* Demonstrated experience in people management, including performance development and team leadership.
* Significant experience supporting clinical trial data analysis and regulatory submissions.
* Excellent problem-solving skills, attention to detail, and the ability to manage multiple priorities under tight timelines.
* Familiarity with R programming is a plus.

To help us track our recruitment effort, please indicate in your email/cover letter where (vacanciesin.eu) you saw this job posting.

yonnetim

Published by
yonnetim

Recent Posts

Family Chartered Legal Executive

Job title: Family Chartered Legal Executive Company: Sacco Mann Job description Sacco Mann are recruiting…

2 minutes ago

163931 Clinical Professor of Psychiatry with special focus on acute psychiatry (fixed-term, 5 years)

Job title: 163931 Clinical Professor of Psychiatry with special focus on acute psychiatry (fixed-term, 5…

6 minutes ago

Budapest Office Project Manager

Job title: Budapest Office Project Manager Company: International Canoe Federation Job description The International Canoe…

16 minutes ago

Team Leader Zespołu Sprzedaży ( praca zdalna )

Job title: Team Leader Zespołu Sprzedaży ( praca zdalna ) Company: Hire Global Spolka z…

22 minutes ago

Account Manager

Location: Texas, United Kingdom Salary: Competitive Type: Permanent Main Industry: Search Sales Jobs Other Industries…

23 minutes ago

Marketing Manager (milan) – North Europe (DACH, Nordics and UK)

Job title: Marketing Manager (milan) - North Europe (DACH, Nordics and UK) Company: Michael Page…

28 minutes ago
If you dont see Apply Button. Please use Non-Amp Version