Clinical Research Associate

BioSpace; Amadora; Híbrido; EUR 42 000 - 64 000; Tempo integral

Resumo da oferta

AbbVie in Amadora, Portugal, is seeking a Clinical Research Associate to join our Clinical Operations team in a hybrid role. You will support delivery of AbbVie studies by building strong partnerships with investigators and site staff, ensuring high-quality conduct and patient safety.

You will work with Phase I-IV studies and gain exposure to a wide range of clinical activities in a collaborative environment.

Qualificações

• Bachelor's degree or equivalent in a health-related or scientific discipline.
• Minimum of one year in clinical research monitoring.
• Strong planning, organizational, communication, and interpersonal skills.
• Good analytical and problem-solving abilities with sound judgment.
• Self-motivated and collaborative with focus on quality and patient safety.

Responsabilidades

• Build partnerships with investigators and site staff to align with study objectives.
• Conduct site qualification, initiation, routine monitoring, and close-out visits.
• Train site personnel on protocol procedures and safety reporting.
• Identify risks and support corrective actions with stakeholders.
• Ensure timely data submission and safety reporting, protecting participants.
• Support patient recruitment and retention by understanding patient journeys.
• Identify investigators and sites using local knowledge and networks.
• Maintain inspection-ready site and study documentation.
• Manage investigator payments and assist with agreements and expense reports.
• Contribute to site engagement strategies with local insights and outcomes.

Conhecimentos

Clinical monitoring

Planning

Organization

Communication

Interpersonal

Analytical thinking

Problem-solving

Collaboration

Quality & compliance

Formação académica

Bachelor's degree

Life sciences background

Descrição da oferta de emprego

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

We are looking for a Clinical Research Associate (CRA) to join our Clinical Operations team in Amadora, Portugal, in a hybrid role. In this position, you will contribute to the successful delivery of AbbVie clinical studies by building strong partnerships with investigators and site staff, ensuring high-quality study conduct, and supporting the protection and safety of study participants.

You will work closely with clinical study teams and investigative sites across Phase IIV studies, gaining exposure to a wide range of clinical research activities in a collaborative and patient-focused environment. This is an excellent opportunity for a motivated clinical research professional to develop their expertise while contributing to the advancement of innovative medicines.

Key Responsibilities

• Build trusted and effective partnerships with investigators and site staff by aligning them with study objectives, protocol requirements, patient treatment principles, and applicable regulatory expectations.
• Conduct site qualification, site initiation, routine on-site and remote monitoring, and study close-out visits for Phase IIV clinical studies, in accordance with the protocol, monitoring plan, GCP, ICH guidelines, AbbVie SOPs, and applicable regulations.
• Train site personnel on the protocol, study procedures, safety reporting requirements, and relevant regulatory expectations, in collaboration with the clinical study team.
• Oversee site activities, proactively identify risks and compliance issues, and support the implementation and follow-up of corrective and preventive action plans in collaboration with Central Monitoring and relevant stakeholders.
• Ensure the quality and timely submission of data from investigative sites, including appropriate reporting and follow-up of safety events, while supporting the protection and safety of study participants.
• Support patient recruitment and retention activities by applying an understanding of the patient journey, therapeutic area, and local site realities.
• Identify, evaluate, and recommend potential investigators and investigative sites, using local knowledge, professional networks, and internal AbbVie resources as appropriate.
• Maintain site and study documentation in an inspection-ready state and support regulatory inspection readiness at assigned sites.
• Manage investigator payments in line with executed contractual obligations, support the negotiation of investigator and hospital agreements with relevant stakeholders, and complete expense reports in accordance with local requirements and applicable guidelines.
• Contribute to site engagement strategies by gathering local insights, tracking progress, reporting outcomes, and identifying opportunities for continuous improvement.

Qualifications

• Bachelors degree or equivalent qualification in a health-related or scientific discipline preferred, such as Medicine, Nursing, Pharmacy, Life Sciences, or a related field.
• Minimum of one year in clinical research monitoring.
• Strong planning, organizational, communication, and interpersonal skills, with the ability to manage multiple priorities and collaborate effectively with study teams, investigators, and site staff.
• Good analytical and problem-solving skills, with the ability to identify site issues, exercise sound judgment, and support appropriate corrective actions.
• Self-motivated and collaborative, with a strong commitment to quality, compliance, patient safety, ethical conduct, and timely delivery.

Additional Information

AbbVie Culture

At AbbVie, we care deeply about bringing innovative solutions to patients in need. By joining us as a CRA, you'll be at the forefront of our mission, working in a dynamic and supportive environment that encourages growth and collaboration.

• All4OneAbbVie: Foster strong interpersonal relationships and teamwork.
• Decide Smart & Sure: Navigate ambiguity and make informed decisions.
• Agile & Accountable: Communicate a clear and inspiring vision.
• Clear & Courageous: Provide honest and constructive feedback.
• Make Possibilities Real: Efficiently plan and execute tasks while adapting to challenges.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html