+34 971 910 842 info@syntaxfs.com


We are looking for professionals who love this challenging work as much as we do

Senior Statistician


As Senior Statistician, you will be working in international project of clinical development supporting all phases of drug development.


Main responsible for the creation of key statistical documents including but not exclusive to:

  • Statistical section of the study protocol
  • Statistical Analysis Plan
  • Tables, Listings and Figures
  • Statistical Report
  • Clinical Study Report
  • Scientific publications

Performs the required programming activities to produce statistical outputs, i.e., tables, listings and figures.

Applies company standards, and actively participates in improvements towards harmonization and standardization across projects.

Maintain and expand knowledge base in area of expertise. Attend courses to develop and keep skills and knowledge current. Comply with continuing  education requirements.

Mentor junior members of the team.


We are looking to speak to candidates with the following attributes:

  • BS or higher degree in Biostatistics, Mathematics or in related field with at least 4 years of experience in clinical development. Or a combination of education, training and work experience.
  • Strong analytic mind-set and logical thinking capability.
  • Ability to select appropriate data assets and design study methodology to achieve the study objectives.
  • Advanced SAS programming and ability to translate study methodology into specifications for programmers.
  • Ability to work on multiple projects and to manage project timelines.
  • Excellent communication skills, and first-hand experience with patient data analysis.
  • Clear written and oral communication concerning the technical aspects of a project and the ability to develop usable documentation in English.
  • Good people-skills and team player.


Palma de Mallorca (Balearic Islands) or remotely.

Clinical Research Associate (CRA) II


We are looking for a CRA based in Barcelona. This is opportunity  will allow you to work closely with a project team in the planning, execution and control of research studies in order to ensure the project and customer needs are met.

As Clinical Research Associate (CRA) you will be in charge assisting in the recruitment and qualification of study sites, collaborating in the training of sites, developing study materials, and coordinating or performing site start-up activities among others.


  • Successful management of investigator sites throughout the site lifecycle, whilst working in accordance with ICH-GCP guidelines, the study protocol, applicable local and international regulatory requirements and internal Standard Operating Procedures.
  • Planning and conducting various site visits (feasibility, site selection, site initiation, site monitoring and close-out) in accordance with the clinical monitoring plan.
  • Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues that have occurred at site.
  • Ensures integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines.
  • Operating as a key part of a global study team.


We are looking to speak to candidates, located in Barcelona, with the following characteristics:

  • Bachelor’s or higher graduate degree withing a Science related field.
  • Able to demonstrate at least 36 months of experience working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment. Please, notice that, because of the position’s requirements, we won’t consider  previous experience as Clinical Research Site Coordinator.
  • Knowledge of ICH-GCP guidelines and local and international regulatory requirements.
  • Ability to communicate effectively with others and excellent time-management and negotiation skills.
  • Good written and verbal communication skills including advanced command of English language.
  • Effective time management and organizational skills.
  • Driving Licence.


  • Competitive salary.
  • Opportunity to progress and development within our Clinical Operations Department.
  • Possibility to work remotely two days per week.


Please send us your CV at lalmirall@syntaxfs.com

Junior Statistical Programmer


We are looking for candidates interested in the fascinating field of clinical research.

As Junior Statistical Programmer you will work closely with the project’s team providing programming and analysis services for specific projects that may include data mining, data analysis, report generation, data quality check, report validation, and clinical software implementations and integrations.


  • Perform the required programming and validation activities to produce statistical outputs, i.e., tables, listings and figures with the support of the Head of Biometry.
  • Primarily work with the Biometry team on ongoing clinical studies to assure results are consistent with expectations, and Quality control procedures are followed.
  • Work with medical writing, clinical operations, and other clinical staff to support deliverables.
  • Attend training to develop skills and knowledge.


We are looking to speak to candidates with the following characteristics:

  • Biostatistics, Mathematics, or Informatics.
  • Computer and arithmetic knowledge, as well as skills to adapt to different computer systems.
  • Strong analytic mind-set and logical thinking capability.
  • Detail oriented, ability to multitask with strong prioritization, planning and organization skills.
  • Ability to manage deadlines.
  • Good team player: Shows support for teamwork, cooperation, self-control, and flexibility to get the job done.
  • Good level of spoken and written English.
  • Experience not requested.


  • Specific training.
  • Permanent contract.
  • Opportunity to progress and development within our organization.


Palma de Mallorca (Balearic Islands)

Do you want to join us?