IRW Consulting is seeking Clinical Research Associates (CRAs) on positions located in Stockholm
IRW Consulting is seeking Clinical Research Associates (CRAs) on positions located in the Stockholm area.
IRW is a full-service Clinical Research Organization (CRO) with more than thirteen years experience and offices in Sweden, Denmark, Norway and Finland. IRW offers solid know-how and experience of clinical research, data-management, biostatistics and pharmacovigilance for global and small pharma, biotech and medical device companies.
You are welcomed to apply for the positions if you have Bachelor or Master’s degree in life sciences, pharmacy or nursing and preferably a minimum of 2 years of clinical research experience in Pharmaceutical industry and/or CRO company.
Clinical Research Associate (CRA)
Qualifications and background:
• Bachelor or Master’s degree in life sciences, pharmacy or nursing.
• Preferably a minimum of 2 years of clinical research experience in Pharmaceutical industry and/or CRO company.
• Be accurate and have a high level of quality conscious.
• Be well organized and adaptive to change.
• Act responsible and be able to work independently.
• Good knowledge of spoken and written English.
• Good organizational skills.
• Ability to work independently in a fast-paced environment.
• Valid driving license.
Main Responsibilities:
• Prepare and complete applications to the regulatory authorities and ethic committees.
• Responsible for completion of study documentation such as CRFs, patient diaries, QoL forms etc.
• Preparing Monitoring Manuals, Source Data Verification plans etc.
• Perform routine site visits, including selection, initiation, interim and closure monitoring visits.
• Manage assigned sites throughout the study by regular contacts to ensure site compliance, adequate enrolment, and understanding of study requirements.
• Participate in Audits and Inspections and assist with company’s quality control initiative.
• Assist in data validation and clean file procedures
• Selecting and negotiating contracts with local/central laboratories, pharmacies etc.
• Planning and participating at Investigators meeting
• Responsible for final archiving of study documents in-house and on-site
• Demonstrate willingness to take on any level project activity consistent with current or past experience in support of study delivery.
Welcome to send your application to : jobs@irwcro.com