Clinical Research Associate II (France)

Alimentiv; Marseille; À distance; EUR 39 500 - 66 000; Plein temps

Résumé du poste

A leading clinical research organization seeks a Clinical Research Associate II to support clinical site monitoring in France. This role offers training in CRA skills and involves site management activities, data review, and fostering stakeholder relations. Ideal for candidates with a college degree and relevant experience, this position offers a yearly salary between €39,500 and €66,000. Regular travel required.

Qualifications

• Minimum of 1-3 years related experience.
• SoCRA, CCRA and/or ACRP certification/designation is an asset.
• Commitment to achieving positive results.

Responsabilités

• Support and observe clinical site monitoring services.
• Conduct remote data review and support data query activities.
• Conduct and document onsite/remote site contacts.

Connaissances

Self-motivation

Strong communication skills

Attention to detail

Formation

College diploma/degree

Description du poste

Clinical Research Associate II (France)

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Primarily a training and development role, this position will support and observe clinical site monitoring services both in-house and in the field whilst developing CRA skills and knowledge. This role will have exposure and training in all aspects of the clinical site monitoring services whilst providing monitoring and site management activities for full-service studies assessing for protocol, SOP, and regulatory compliance. Responsibilities include site management activities to help drive investigative site and patient recruitment, compliance, and oversight. Conduct remote data review, support data query and closure activities, support Risk Based Monitoring (RBM) activities, assess data collection and (regulatory) document collection, perform remote and onsite activities for investigational sites including site contacts, qualification, initiation, monitoring and close out visits under supervision and/or independently and in accordance with corporate, sponsor and regulatory (ICH GCP and other) standards and guidelines. Represents the corporation by maintaining collaborative relationships with stakeholders.

Site Management

• Conduct and document remote site contacts which could include remote site initiation, monitoring and close out visits. Document activities per SOPs and study guidance.
• Conduct and document onsite activities such as feasibility, qualification, initiation, monitoring and close out visits under supervision. Document activities per SOPs and study guidance.
• Conduct remote data review of EDC, CTMS, RBM and other clinical systems to ensure alignment with SOPs, study guidelines and GCP best practices. Identify trends within and across study sites and escalate findings appropriately.
• Routinely review the site section of the TMF for accuracy, timeliness, and completeness. Request new/updated documents from the site/primary assigned CRA, as required.
• Support CRA II, Senior CRA and Lead CRA’s in day-to-day study management activities.
• Remotely monitor, resolve, and/or facilitate resolution of queries arising out of regular and/or safety reviews, adverse events, and other data management activities throughout the trial.
• Coordinate delivery of clinical sites communications, collaborating with project teams, to ensure investigational sites are provided accurate ongoing data, updates, information and feedback on project/regulatory guidelines and objectives throughout the project life cycle.
• Supports preparation for audit and required follow-up actions.

Site Setup and Startup Support

• Identify and recruit site investigators, coordinate the movement and delivery of trial materials, samples, tests, and forms, including investigational medicinal product, protocols, SOPs, CRFs, project documents, forms, and support tools.
• Ensure SOPs in place to optimize patient recruitment providing guidance to site teams of inclusion/exclusion criteria.

Training and Development

• Successfully complete CRA development track activities and milestones.
• Develop and demonstrate competencies required to fulfill the role of a CRA.
• Support and observe primary assigned CRAs at both onsite and remote visits.
• Support Lead CRA’s with remote site management activities.
• Participate in all study related activities, including but not limited to trainings, team meetings and provide any necessary updates to the study team.

Qualifications

• The successful candidate will possess a minimum of a college diploma/degree and 1-3 years related experience.
• SoCRA, CCRA and/or ACRP certification/designation is an asset.
• The successful candidate must exhibit the following skills: self-motivation with strong communication skills and a commitment to achieving positive results.
• Strong attention to detail and keenness to understand the importance of building collaborative relationships to achieve results.
• For one CRA position supporting Flemish sites in Belgium, Dutch language skills are required.

Working Conditions

• Home-based
• Regular travel

€39,500 - €66,000 a year

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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Seniority level: Entry level; Employment type: Full-time; Job function: Research, Analyst, and Information Technology; Industries: Pharmaceutical Manufacturing.