Job Brief:

We are looking for a SQL Server Developer with strong database expertise to support the development and optimization of data solutions within our technology team.

Responsibilities:

• Develop and maintain SQL Server database components, including stored procedures and functions.

• Optimize queries, stored procedures, and database performance to ensure efficient data processing.

• Support the design and implementation of advanced SQL queries and database structures.

• Collaborate with technical teams to ensure reliable and scalable database solutions.

Requirements & Skills:

• Bachelor’s degree in Computer Science, Information Systems, or a related field.

• Minimum 3 years of experience with SQL Server.

• Strong experience writing stored procedures, functions, and advanced SQL queries, including database tuning and optimization.

• Familiarity with DevOps practices is considered a plus.

• Professional working proficiency in English and Portuguese.

• Ability to work in a hybrid setup (2 days per week in the Lisbon office).

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Job Brief:

The Senior Clinical Trial Assistant (Sr CTA) will provide high-level administrative, operational, and project tracking support to Project Managers and Clinical Trial Managers across all phases of clinical trials. This role is critical to ensuring inspection readiness, accurate trial tracking, and smooth coordination of study activities within a global clinical research organisation that delivers end-to-end clinical development services.
The position is hybrid, requiring presence in the office twice a week to foster team collaboration while maintaining flexibility.

Responsibilities:

• Provide administrative and trial coordination support across all study phases (start-up, execution, close-out).
• Support inspection readiness and quality oversight activities.
• Track trial progress, timelines, milestones, and deliverables; generate reports and metrics as required.
• Maintain accurate and up-to-date trial information in CTMS and related systems.
• Support Trial Master File (TMF) management, ensuring completeness, quality, and timely filing.
• Coordinate internal and external meetings, including documentation and follow-up.
• Assist with site and country feasibility, site selection, and vendor set-up.
• Support Investigational Product (IP) and ancillary supply tracking.
• Track trial and country budgets, support invoice reconciliation, and follow up on variances.
• Set up and track trial-specific training requirements.
• Collaborate with internal teams and external partners, including CROs and vendors.
• Support database lock activities, audits, and Health Authority inspections.
• Contribute to process improvement initiatives as needed.

Requirements & Skills:

• Minimum 2 years of experience as a Clinical Trial Assistant (CTA).
• Bachelor’s or Master’s degree in Life Sciences or a related field.
• Solid understanding of GCP, regulatory requirements, and clinical trial processes.
• Experience working with CTMS or other clinical trial systems.
• Excellent organizational, planning, and time management skills.
• Strong written and verbal communication skills in English language.
• Ability to manage multiple priorities and work independently in a fast-paced environment.
• Advanced proficiency in Microsoft Office and strong ability to learn new technologies.
• Strong attention to detail with a focus on quality, compliance, and inspection readiness.

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Job Brief:

We are looking for a Market Access Consultant to join our team and lead strategic market access projects within the pharmaceutical industry. The role involves identifying, building, and communicating the clinical, social, and economic value of pharmaceutical products, supporting pricing, reimbursement, and market positioning in highly regulated environments.

Responsibilities:

• Develop and support market access and public affairs strategies for pharmaceutical products.
• Build and communicate product value stories, integrating clinical, economic, and outcomes evidence.
• Prepare and adapt value dossiers, payer negotiation materials, and hospital formulary submissions (e.g. GÉNESIS).
• Conduct comparative value assessments versus competitors and standard of care.
• Contribute to HEOR and pharmacoeconomic projects, including budget impact and cost-effectiveness analyses.
• Participate in and support advisory boards and strategic consensus initiatives (e.g. Delphi panels).
• Collaborate with internal teams and clients to ensure high-quality, timely project delivery.

Requirements & Skills:

• Bachelor's degree in Pharmacy, Life Sciences, Health Sciences, Economics, Biomedicine, Biotechnology, or a related field.
• 5+ years of experience in Market Access, HEOR, pharmaceutical consulting, or similar roles within the life sciences industry.
• Strong understanding of the Spanish healthcare system and pricing and reimbursement processes (European experience is a plus).
• Proven experience developing value dossiers, negotiation materials, and market access documentation.
• Ability to lead projects with a high level of autonomy and accountability.
• Strong analytical skills with the ability to interpret and synthesize clinical and economic data.
• Strategic mindset with a consulting-oriented and client-focused approach.
• Fluent Spanish and advanced English (both written and spoken).
• Advanced proficiency in Excel and PowerPoint.

Your Next Challenge Awaits!

Ready to take your career to the next level? Submit your application and explore the impact you can make with us!