Clinical Research Associate (CRA)

Job title:

Clinical Research Associate (CRA)

Company:

NonStop Consulting

Job description

Clinical Research Associate (CRA) – Flexible Work EnvironmentOur client, a prominent leader in the clinical research sector, provides an exceptional opportunity for professional advancement. Known for its dedication to superior quality and ethically-focused research, the organization fosters professional development through active engagement in cutting-edge oncology trials and regulatory activities, including Clinical Trials Information System (CTIS) submissions. This role is located in Melle, Belgium, with the flexibility to work either from home or the office, tailored to your preference.BenefitsJoining our client’s team will present you with the following advantages:– Flexible working environment: Options to work remotely or from the office in Melle.– International collaboration: Collaborate with international study teams and travel to countries such as the Netherlands, the UK, France, and Germany.– Broaden your expertise: Gain exposure to advanced oncology trials and regulatory activities, enriching your professional skills and experience.Role ResponsibilitiesIn the capacity of a Clinical Research Associate, your principal responsibilities will include:– Conducting Site Initiation Visits (SIVs), Site Monitoring Visits (SMVs), and Site Closeout Visits (SCOVs) to ensure adherence to study protocols and regulatory requirements.– Engaging in international collaborations and traveling for monitoring purposes, aligning with the organization’s mission to maintain high clinical trial standards.

– Participating in department-wide tasks aimed at process optimization and maintaining an updated personal dossier, including training records and CV.RequirementsThe ideal candidate will exhibit the following qualifications and skills:– A degree in life sciences, preferably a higher vocational education or academic degree, with a minimum of 1-2 years of experience as a Clinical Research Associate.– Proficient in Dutch, with fluency in French and English, alongside exceptional knowledge of ICH-GCP and applicable regulatory requirements.– Strong communication skills, problem-solving abilities, and the capacity to work independently, with a willingness to travel internationally for monitoring purposes.Closing StatementIf you are a committed professional seeking to thrive in a flexible and ethically-driven work setting, we invite your application for this role. Join our client’s esteemed team and contribute significantly to the success of pioneering clinical research initiatives across Europe.

Expected salary

Location

Belgique

Job date

Sat, 02 Nov 2024 07:18:35 GMT

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