Clinical Research Assoicate

Job Description

We are seeking a highly skilled Clinical Research Associate (CRA) to lead performance and compliance for assigned protocols and sites within Portugal - Zona Norte. Under the oversight of the CRA Manager, you will serve as the primary site contact throughout all phases of clinical studies, ensuring rigorous adherence to ICH/GCP, local regulations, our company policies and procedures, quality standards, and adverse event reporting requirements.

You will take ownership of allocated sites, actively collaborate in expanding our clinical research territory by identifying and developing new sites and contribute as a subject matter expert on monitoring processes and systems across internal workstreams.

The person must live in north of Portugal (Porto).

What You Will Do

- Build and sustain strong relationships with investigative sites across all trial phases.

- Perform site management and monitoring activities in compliance with ICH‑GCP, Sponsor SOPs, local laws/regulations, protocol, site monitoring plans, and related documents.

- Execute validation, initiation, monitoring, and close‑out visits; document clear, comprehensive visit and non‑visit reports in a timely manner.

- Coordinate cross‑functional tasks to achieve Site Ready status.

- Identify, assess, and resolve site performance, quality, or compliance issues; elevate appropriately per the CRA escalation pathway in collaboration with CRA Manager, Clinical Research Manager and Clinical Research Director.

- Act as a process subject matter expert, share best practices, drive continuous improvement, and deliver training.

What Skills You Will Need

- Bachelor’s degree (or higher) with at least 3 years of direct site management (monitoring) in bio/pharma/CRO.

- Applicants must possess a valid driver’s license.

- Fluent in English, with strong written and verbal communication skills and the ability to present technical information effectively.

- Robust knowledge of clinical research, trial phases, ICH/GCP, and local clinical research regulations and guidelines; ability to work within global, country, and regional frameworks.

- Proven site management expertise, including independent oversight of site performance and patient recruitment.

- Hands‑on knowledge of Good Documentation Practices.

- Strong IT proficiency (MS Office and clinical applications across computer, tablet, and mobile); adaptable to new tools.

- Ability to interpret data/metrics and take appropriate action.

- Excellent time management, organization, interpersonal skills, conflict management, and problem solving.

- Strong sense of accountability and urgency; able to prioritize and multitask in changing environments. Positive, growth‑oriented, self‑driven, and professional demeanor aligned with company values.

Why Join Us?

We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world’s most challenging healthcare needs.

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment.

So, if you are ready to please apply today.

Required Skills

- Accountability

- Accountability

- Adaptability

- Adverse Event Reporting System

- Clinical Research Methods

- Clinical Site Management

- Clinical Study Management

- Clinical Trial Planning

- Clinical Trials

- Clinical Trials Monitoring

- Data Analysis

- Data Integrity

- Data Reporting

- Driving Continuous Improvement

- Good Clinical Data Management Practice (GCDMP)

- Good Clinical Practice (GCP)

- Investigation Procedures

- IS Audit

- Maintenance Management

- Medical Research

- Oral Communications

- Patient Safety

- Protocol Adherence

- Quality Standards

- Regulatory Compliance

- {+ 3 more}

Requisition ID

R378757

Job Posting End Date

01/15/2026

A job posting is effective until 11:59:59 PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

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