Job Description
The organization of international clinical trials requires the development of complex cross-cultural teams across borders, languages and time-zones. At SCOPE International we recognize that recruitment, training and retention of talented employees is fundamental to building high performing teams. Our success is built upon encouraging talented people to join SCOPE and further training them continuously and systematically to develop their skills and achieve their full potential. We actively seek out recruits who exhibit our key values of customer orientation, entrepreneurial thinking, conscientiousness and reliability. As a socially responsible company, we offer an attractive working environment with an open and flexible employment philosophy, thereby providing working environments conducive to an international setting, coupled with excellent career development prospects and a management culture that is based on an open dialogue. SCOPE International is an independent Full-Service Contract Research Organization (CRO) with a network of 16 local offices and business entities throughout Europe and USA. SCOPE offers a complete range of clinical development and consulting services to the pharmaceutical, biotechnology and medical device industries, and is supported by long established partnerships in other geographies. Our experience and expertise in managing all major indications in clinical phases I – IV makes us the perfect partner for companies looking to work closely together to develop custom solutions and seeking guidance through all development phases. For our Head office in Germany we are looking for a professionally experienced and enthusiastic personality For our UK office (Bolton) we are looking for a professionally experienced as well as collaborative and enthusiastic personality: Tasks & Responsibilities Main contact to the research team to ensure timely initiation, recruitment and completion of clinical trials Responsible for the identification, evaluation and qualification of investigators and sites Collects and reviews essential documents received from clinical sites to ensure all required documents obtained are accurate and complete Collects, reviews and submits documents for relevant CAs and ECs / IRBs Reviews and monitors data on site and remotely; resolves issues on a continuous basis to achieve timely database lock targets Oversees site’s performance and study data completion within the electronic systems Reviews, maintains and updates project-related data in existing systems, e.g. CTMS, eTMF, etc. Qualifications & Requirements Bachelor’s degree in a life science or related field of study; or equivalent combination of studies, nursing qualifications, and / or work experience 1 – 2 years of experience as Clinical Research Associate Good knowledge of GCP-ICH and local regulations regarding clinical studies Very good proficiency in English (both spoken and written) Willingness and ability to travel Proficient knowledge of Microsoft Office Responsible, conscientious and results oriented with excellent communication skills
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