The role

The Study Director is the key figure in the execution and control of each study. From protocol approval to the signature of the final report, they assume overall responsibility for the study and ensure that every phase is carried out to the highest scientific, administrative and regulatory standards, the pillars of Versa Biomedical’s Certified Rigor Framework.

Key responsibilities:

• Centralise control of the study and assume overall responsibility for its execution and final report.
• Coordinate the laboratory management, study team and quality assurance personnel, ensuring effective communication throughout all phases.
• Approve, sign and date the protocol and any subsequent amendments.
• Oversee data collection, analysis and presentation; draft and review study conclusions.
• Ensure compliance with Good Laboratory Practice (GLP) principles throughout the study.
• Ensure that the protocol, amendments and SOPs are available and up to date for the entire team.
• In multi-site studies, clearly define and document the role of each principal investigator, laboratory and participating test facility.
• Assess and document the impact of any deviation on the quality and integrity of the study, activating corrective actions where necessary.
• Ensure all raw data are recorded completely and traceably.
• Validate computerised systems used in the study, where applicable.
• Archive the protocol, final report, raw data and supporting material upon study completion.

Your profile

Required qualifications:

• Degree in Health Sciences (Veterinary Medicine, Pharmacy, Biology or similar).
• Training in regulation, handling and use of laboratory animals.
• Knowledge of Good Laboratory Practice (GLP).
• English at an intermediate-advanced level (minimum B2), both spoken and written.
• Catalan at a full professional level, both spoken and written.

Additional qualifications (valued):

• PhD in science.
• Knowledge of ISO 13485.
• Laboratory Animal Science course (functions A-D).

Experience:

• Hands-on experience in laboratory techniques.

What defines you:

• Rigorous mindset, results-oriented.
• Strong organisational skills and ability to manage priorities.
• Ability to solve problems autonomously and with sound judgement.
• Natural team player with a cross-functional leadership approach.

Versa Biomedical culture — A team fond of challenges

At Versa Biomedical, we are not simply looking to fill a position. We are looking for people who are driven by difficult questions, who find satisfaction in precision, and who understand that behind every study there is a patient we are impacting.

We are a small, diverse and committed team based in the metropolitan area of Barcelona. We work in an open environment, literally and in philosophy, where collaboration with surgeons, external experts and international sponsors is part of everyday life.

We believe in science with purpose. We are aligned with the United Nations Sustainable Development Goals and actively work to make our activity more sustainable, responsible and equitable.

What we offer

• Real impact. Your work directly contributes to the development of treatments and devices that reach real patients around the world.
• A reference methodology. You will work within Versa Biomedical’s Certified Rigor Framework — triple certification GLP, ISO 13485 and ISO 9001 — in an environment where excellence is the standard, not the exception.
• Flexibility and trust. Autonomy to manage your work responsibly, within a team that values professional judgement.
• Continuous development. Training, participation in congresses and projects that constantly expand your expertise.
• Shared purpose. You will be part of a growing company with a clear mission: open models, open futures.

Ready to lead studies that open futures? Send us your application at versa@versabiomedical.com

Open models, open futures. Join us.