Clinical Research Associate

Alimentiv; Porto; Presencial; EUR 41 000 - 83 000; Tempo integral

Resumo da oferta

Upsilon Global seeks a Freelance Clinical Research Associate (CRA) to join their Portugal operations. The role focuses on on-site monitoring, study start-up support, and SDV activities, with regular site communication and global project collaboration.

The ideal candidate holds a Life Sciences degree, has on-site monitoring experience in Portugal, and is fluent in English. Travel willingness is required, and MS Office skills are essential for daily tasks within a flexible, project-based

Qualificações

• Degree in Life Sciences or an equivalent combination of education, training, and experience.
• Independent on-site monitoring experience in Portugal.
• Experience in Oncology or Gastroenterology is beneficial.
• Full professional proficiency in English.
• Proficiency in Microsoft Office applications.
• Strong planning, multitasking, and organisational skills.
• Excellent communication, collaboration, and problem-solving abilities.
• Willingness and ability to travel.

Responsabilidades

• Conduct and report on all types of on-site monitoring visits.
• Support study start-up activities.
• Perform CRF review, source data verification (SDV), and query resolution.
• Manage investigator sites and maintain regular site communication.
• Act as a key point of contact for internal support teams and external vendors.
• Communicate study progress with internal project teams.
• Participate in feasibility assessments.
• Support the Regulatory team with the preparation of study submission documentation.

Conhecimentos

On-site monitoring experience

English proficiency

MS Office

Planning & multitasking

Communication & collaboration

Willingness to travel

Formação académica

Degree in Life Sciences

Descrição da oferta de emprego

Freelance Clinical Research Associate (CRA) – Portugal

Upsilon Global is seeking a Freelance Clinical Research Associate (CRA) on behalf of an established mid-sized CRO to join their Clinical Operations team in Portugal.

This CRO has developed a reputation as a leading employer within Clinical Operations, offering excellent growth opportunities and career progression through a variety of career pathways and personal development programmes.

Despite expanding into a leading mid-sized CRO, they have retained their "small company" culture, with a flat management structure that enables smoother communication, faster decision-making, and greater opportunities for career progression.

• Start Date: ASAP
• Contract Type: Freelance
• Company Type: Mid-sized CRO
• Therapeutic Areas: Haematology and Gastroenterology
• Location: Northern Portugal

Key Responsibilities

• Conduct and report on all types of on-site monitoring visits.
• Support study start-up activities.
• Perform CRF review, source data verification (SDV), and query resolution.
• Manage investigator sites and maintain regular site communication.
• Act as a key point of contact for internal support teams and external vendors.
• Communicate study progress with internal project teams.
• Participate in feasibility assessments.
• Support the Regulatory team with the preparation of study submission documentation.

Requirements

• Degree in Life Sciences or an equivalent combination of education, training, and experience.
• Independent on-site monitoring experience in Portugal.
• Experience in Oncology or Gastroenterology is beneficial.
• Full professional proficiency in English.
• Proficiency in Microsoft Office applications.
• Strong planning, multitasking, and organisational skills.
• Excellent communication, collaboration, and problem-solving abilities.
• Willingness and ability to travel.