Clinical Research Unit Lead — Strategy & Trials

Institut d'Investgació i Innovació Parc Taulí (I3PT); España; On-site; EUR 90,000 - 130,000; Full time

Benefits offered by this job

Immediate start

Flexible working hours

Collaborative environment

Full-time 37.25 hours per week

Job summary

Institut d'Investgació i Innovació Parc Taulí (I3PT) is seeking a Head of the Clinical Research Unit to coordinate the clinical research area, supervise SOPs, and lead trials in collaboration with OTAC and USAC. The role requires a strong background in biomedical sciences, management experience, and English proficiency.

You will drive strategic objectives, foster external partnerships, and ensure compliance and high-quality research outputs within a collaborative hospital setting.

Qualifications

• Bachelor's degree plus Official Master's in Biomedical Sciences or related field required.
• C1 level of Catalan required.
• Minimum 5 years of professional experience in clinical research, incl. coordination and management of trials.
• Experience leading research projects and teams preferred.

Responsibilities

• Coordinate the clinical research area and cross-cutting processes.
• Lead start-up procedures for clinical studies with OTAC and USAC.
• Negotiate framework agreements with sponsors and manage budgets.
• Provide methodological advice on study design and feasibility.
• Draft and maintain SOPs across the area.
• Manage USAC HR and training needs.
• Report to Management and participate in committees.

Skills

Leadership

Team management

Strategic mindset

English proficiency

Negotiation skills

Communication skills

Education

Bachelor's + Official Master's in Biomedical Sciences

MBA or business development training

PhD in biomedical research

Master in Clinical Trial Monitoring/Coordination

Tools

Office software

Job description

Institut d'Investgació i Innovació Parc Taulí (I3PT) is seeking a Head of the Clinical Research Unit to coordinate the clinical research area, supervise SOPs, and lead trials in collaboration with OTAC and USAC. The role requires a strong background in biomedical sciences, management experience, and English proficiency.

You will drive strategic objectives, foster external partnerships, and ensure compliance and high-quality research outputs within a collaborative hospital setting.