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Senior Clinical Research Associate
PSI CRO AGSenior Clinical Research Associate at PSI managing relationships and compliance in clinical research. Ensuring timelines and standards while working with various project stakeholders across therapeutic indications.
About the role
Key responsibilities & impact- As a Senior CRA, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications.
- You will build and maintain relationships with clinical sites and investigators.
- Your focus will be on subjects’ rights, safety and well-being and quality of data compliance.
- Responsibilities will include conducting and reporting all types of onsite monitoring visits, driving the study startup phase, performing CRF reviews, source document verification and query resolution.
Requirements
What you’ll need- BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience
- Independent on-site monitoring experience in the Netherlands
- Demonstrable experience in all types of monitoring visits in Phase II and/or III
- Strong written and verbal communication skills
- Fluency in Dutch and English
- Experience supporting Oncology studies is beneficial, but not essential
- Advanced knowledge of MS Office
- Full and clean driver's license, and the ability to travel
- Communication, collaboration, and problem-solving skills are essential
- Ability to multitask and work in a dynamic team environment
Benefits
Comp & perks- Make the right call and take your career to a whole new level.
- Join the company that focuses on its people and invests in their professional development and success.
- Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way.
- We will guide and support you with information, making your experience as smooth as possible.
ATS Keywords
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Hard Skills & Tools
on-site monitoringCRF reviewssource document verificationquery resolutionclinical researchPhase II studiesPhase III studiesdata complianceclinical trial managementtherapeutic indications
Soft Skills
communication skillscollaboration skillsproblem-solving skillsmultitaskingrelationship buildingindependenceadaptabilityteamworkattention to detailtime management