Senior/CRA - Sweden

Proclinical's client is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Their mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach. We leverage local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.

Job Responsibilities:

• Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas
• Perform source document verification and case report form review
• Perform regulatory document review
• Conduct study drug inventory
• Perform adverse event and serious adverse event reporting and follow-up
• Assess patient recruitment and retention.

Skills and Requirements:

• Bachelor of Science in health-related field (a BSN is preferred);
• Min. 2 years of proven CRA experience;
• Broad knowledge of medical terminology and clinical patient management;
• Basic knowledge of drug therapy techniques and clinical research methodologies;
• Fluency in local language and excellent English.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Sigrid Jorgensen on +44 203 856 9337 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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