Senior Clinical Research Associate

TFS HealthScience; Campo de Ourique; Presencial; EUR 40 000 - 60 000; Tempo integral

Resumo da oferta

A leading global Contract Research Organization is seeking a Senior Clinical Research Associate in Lisbon. The role involves monitoring clinical trials, ensuring participant safety, and maintaining data integrity. Qualified candidates should have a Bachelor’s degree in life sciences and over 3 years of CRA experience. The company offers competitive compensation and career growth in a collaborative environment.

Serviços

Competitive compensation package

Comprehensive benefits

Opportunities for personal and professional growth

Qualificações

• 3+ years of experience as a CRA including relevant on-site monitoring experience.

Responsabilidades

• Monitor on-site and remotely clinical trials.
• Perform monitoring activities to ensure subjects' safety and data integrity.
• Verify informed consent procedures and protocol requirements.
• Review CRFs and subject source documentation for accuracy.

Conhecimentos

Experience with Medical Devices

Ability to work in a fast-paced environment

Formação académica

Bachelor’s Degree in life science or nursing

Descrição da oferta de emprego

Overview

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.

Join Our Team as a

Senior Clinical Research Associate

About this role

As part of our Strategic Resourcing Solutions (SRS) team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals.

The Senior Clinical Research Associate is responsible for the initiation, on-site and/or remote monitoring and close out of study sites during study conduct, according to company policies, SOPs and regulatory requirements.

Key Responsibilities

• Monitor on-site and remotely clinical trials in accordance with TFS and/or sponsor Standard Operating Procedures GCP and ICH guidelines and applicable regulatory regulations.
• Perform all required monitoring activities at the study sites to assess and ensure subjects safety, data integrity and quality.
• Verify the protection of study participants by informed consent procedures and protocol requirements that follow appropriate regulations.
• Review CRFs (electronic or paper) and subject source documentation for validity and accuracy.

Qualifications

• Experience working with Medical Devices.
• Bachelor’s Degree, preferably in life science or nursing; or equivalent.
• >3 years of experience as CRA including relevant on-site monitoring experience.
• Able to work in a fast-paced environment with changing priorities.

What We Offer

We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in the lives of patients.

A Bit More About Us

Our journey began over 25 years ago in Sweden, in the city of Lund. As a global CRO with the ultimate goal of ensuring patients’ safety and well-being, we provide biotechnology and pharmaceutical companies with tailored clinical development solutions. We currently operate in 17 countries across Europe, North America, Asia Pacific and the Middle East.

Our core values of Trust, Quality, Flexibility and Passion are what make TFS Healthscience the successful company it is today. Our values shape our culture and work ethic. They reflect what we stand for and guide our organization.

#Together we make a difference