Clinical Research Associate II / Senior CRA (Spanish, Portuguese & English fluency)

Ergomed; Lisboa; Hybrid; EUR 42,000 - 65,000; Full time

Job summary

Ergomed is seeking a Clinical Research Associate to perform on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visits across Spain and Portugal, ensuring sites meet study requirements.

The role requires extensive Phase 2/3 monitoring experience, particularly in oncology or rare diseases, and fluency in English, Spanish, and Portuguese. Travel is essential, with collaboration across a global team.

Qualifications

• Degree in Life Sciences or equivalent required.
• Extensive on-site monitoring experience in phase 2/3 trials, ideally with oncology/rare indications.
• Fluent in English, Spanish & Portuguese.
• Ability to plan, multitask and work in a dynamic team environment.
• Willingness to travel.

Responsibilities

• Perform on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visits in Spain and Portugal.
• Identify investigators and verify qualifications, resources, facilities and staff for study conduct.
• Train investigational site staff as necessary.
• Support preparation of regulatory submissions when applicable.

Skills

Life sciences degree

On-site monitoring

English, Spanish, Portuguese

Travel willingness

Education

Life sciences degree

Job description

Company Description

Medicine moves forward here. So will you.

Ergomed is a specialist clinical research organization focused on rare disease and select oncology indications. We focus on the most complex trials, the studies where experience, judgement, and rigorous operational accountability make the biggest difference. We partner with small to midsize biotech companies to move promising therapies through early phase development, so they reach the patients sooner.

We choose complex work on purpose. Rare disease and oncology trials carry real operational risk, and our people are experts at reducing it, protecting timelines, data quality and the experience of sites and patients at the same time. It is demanding, meaningful work, and no one here forgets that patients cannot wait.

That is why culture matters to us as much as capability. We have built a collaborative, international team where people share ideas, grow their careers and are trusted to take ownership early. With colleagues across North America, South America, Europe, Asia and Australia, we value teamwork, flexibility and a real commitment to work-life balance, because good science comes from people who feel supported.

If you want work with purpose, the agility to make an impact and a team that cares about the people behind the work as much as the work itself, we would love to hear from you.

Job Description

Performs on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities in both Spain and Portugal to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study

Identifies the investigators and verifiesthat the investigator has adequate qualifications,resources, facilities, equipment and staff toconducting the clinical study throughout the study period.

Trains investigational site staff as necessary

When applicable, supports preparation of regulatory and / or EC submissions

Qualifications

• - College/University degree in Life Sciences or an equivalent combination of education, training & experience
• - Extensive on-site monitoring experience in phase 2/3 trials, ideally with experience of complex trials such as oncology / rare
• - Full working proficiency in English, Spanish & Portuguese
• - Ability to plan, multitask and work in a dynamic team environment
• - Communication, collaboration, and problem-solving skills
• - Ability to travel

Additional Information

• - Quality: we hold ourselves to the standard patients deserve.
• - Integrity and trust: we do the right thing, especially when it is hard.
• - Drive and passion: we care about the outcome, because someone is waiting on it.
• - Agility and responsiveness: we move quickly, because patients cannot wait.
• - Belonging: everyone is welcome, and every voice counts.
• - Collaborative partnerships: we go further by going together.

When you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. You’ll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.

We are diverse in many ways, yet our values unite us. Our values are how we work, not words on a wall. If they sound like you, you will feel at home here.

We look forward to welcoming your application.