IRW Consulting is seeking Clinical Research Managers
IRW Consulting is seeking Clinical Research Managers (CRMs) 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 6 years clinical research experience including 3 years project management/Assistant PM or as Clinical Team Lead.
Clinical Research Manager (CRM)
Qualifications and background:
• Bachelor or Master’s degree in life sciences, pharmacy or nursing.
• Preferably a minimum of 6 years clinical research experience including 3 years project management/Assistant PM or as Clinical Team Lead.
• Experience in a key Pharmaceutical/CRO operational function, e.g. data management, clinical operations, laboratory, pre-clinical; or equivalent combination or educations, training and experience.
• Accurate and have a high level of quality conscious.
• Well organized and adaptive to change.
• Act responsible and be able to work independently.
• Have strong interpersonal skills and the ability to build relationships both internally and externally.
• Good ability to express oneself both verbally and in writing.
• High level of organizational skills.
• Excellent interpersonal and organizational skills and the ability to build relationships both internally and externally.
• Strong written and verbal communication skills including good command of English language.
• Ability to work independently in a fast-paced environment.
• High ability to priorities and handle several tasks simultaneously.
• Valid driving license.
Main Responsibilities:
• Manage project budget and timelines.
• Ensures communication is maintained and reporting schedules are adhered to.
• Produce and distribute reports and presentation materials.
• Ensure that work is conducted in compliance with standard operating processes, policies and procedures and meets quality and timeline metrics.
• Prepare and complete applications to the regulatory authority and ethics committees.
• Prepare instructions to investigators and other site study staff.
• Plan, participate and lead Investigator Meeting and CRA training when required.
• Prepare Clinical Management Plan.
• Order and organize study supplies.
• Perform routine monitoring visits (selection, initiation, interim and closure visits).
• Assist the Quality Assurance Manager, etc during audits and/or inspections in-house or on site.
• Assist in data validation and clean file procedures.
• Provide input to line managers of their project team members’ performance.
• Provides training for colleagues on any procedures and processes.
• Demonstrate willingness to take on any level project activity consistent with current or past experience in support of study delivery.
• Select and negotiate contracts with 3rd party providers.
• Participate in feasibility studies.
• Assist with company’s quality control initiative.
Welcome to send your application to: jobs@irwcro.com