Biostatistics Technician

Solutiaghs; Barcelona; Presencial; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

A specialized recruitment firm in Barcelona is seeking a Biostatistician to support clinical trials. The ideal candidate will have a Master's degree in statistics or related fields and at least 2–3 years of experience in a biotech environment. Responsibilities include supporting trial planning, ensuring statistical quality, and collaborating with external partners. This role offers a permanent contract with a hybrid work model and competitive salary.

Servicios

Permanent contract

Hybrid work model

Flexible schedule

Competitive salary

Formación

• 2-3 years of experience in a CRO or pharma/biotech setting.
• Solid knowledge of clinical trial statistics and data handling.
• Strong communication skills in English and Spanish.

Responsabilidades

• Support planning, execution, and oversight of clinical trials.
• Review Statistical Analysis Plans (SAPs) and ensure compliance.
• Extract and analyze trial data for regulatory meetings.

Conocimientos

Analytical & problem-solving mindset

Strong organizational skills

Excellent communication abilities

Interpersonal abilities

Educación

Master’s degree in (Bio)Statistics or related field

Descripción del empleo

Overview

Solutia Life Sciences is the recruitment division of Solutia, specializing in technical and middle management roles within the pharmaceutical, biotech, and medical device sectors.

We are seeking a Biostatistician to join a to join a clinical-stage biotech company located in the Maresme area. This is a hands-on role, ideal for a proactive and autonomous professional who enjoys taking responsibility and actively contributing to clinical trial operations. The position reports functionally to an external advisor and collaborates closely with CROs and internal operations.

Responsibilities

• Support the planning, execution, and oversight of clinical trials, ensuring statistical quality and consistency.
• Review and discuss Statistical Analysis Plans (SAPs) and outputs generated by CROs, ensuring accuracy and compliance.
• Extract and analyze trial data to provide insights for meetings with regulatory authorities and internal stakeholders.
• Collaborate with the external advisor, data management team, and CROs to validate and correct statistical outputs.
• Monitor project timelines and follow up on deliverables, ensuring smooth progress of clinical programs.
• Participate in trial meetings and coordinate with operations for seamless trial execution.
• Support methodological improvements and maintain awareness of best practices in biostatistics and clinical trial design.

What They Offer

• Permanent contract
• Hybrid work: 3 days in-office / 2 days remote
• Flexible schedule: Core availability required between 10 a.m and 4 p.m
• Competitive salary

Requirements

• Master’s degree in (Bio)Statistics, Data Management, or a related field (IQS, UB Autónoma or equivalent).
• Minimum of 2–3 years of experience in a CRO or pharma / biotech setting.
• Solid knowledge of clinical trial statistics, data handling, and different trial designs.
• Familiarity with data management principles and ability to liaise with external providers.
• Proactive, autonomous, and organized with strong attention to detail.
• Ability to work independently while coordinating with CROs and internal stakeholders.
• Strong communication skills in English and Spanish.

Skills

• Analytical & problem-solving mindset
• Strong organizational skills & attention to detail
• Excellent communication & interpersonal abilities
• Able to work independently and in cross-functional teams