Clinical Research Specialist(Level 2) (12 Month Contract)

Duties & Responsibilities: - Responsible for the training, mentoring and development of CRS Level 1, including the preparation and development of training materials and tools  - Assisting with the updating of clinical operations process guides  - Responsible for quality checking previously developed projects as part of risk assessment  - Involved in the assessment of client documents prior to project development to determine project timelines  - As delegated, will assist in the planning and backlog of projects  - Analyse, understand, and process complex scientific/medical/pharmaceutical information  - Work with study teams and internal project teams to ensure timely delivery of high-quality solutions  - Execute the layout and structure of clinical information required to utilize our products efficiently and effectively  - Monitor, analyze, and action end user feedback and usage analysis metrics to evaluate and improve usability and accuracy of our products  - and successfully complete the ‘In-House Clinical Trial Training Programme’ (within 6 -12 months) and gain an in-depth knowledge of trial design, trial procedures, operational daily trial activities etc., in preparation for Level 3 activities - Undertake other duties in-line with your role and business requirements as required Experience Required: - Superb editorial skills with a keen eye for text and graphic layouts - Proven ability to organize information in a logical and systematic way - Ability to focus on fine details and the wider system at the same time - Extreme attention to detail and accuracy even when balancing multiple projects - Highly adaptable and flexible - Ability to quickly and easily switch contexts, particularly between creative and analytical work - Exceptional analytical and logical skills with highly developed critical thinking, problem-solving and decision-making skills - Passion for creative solutions, innovation, and divergent thinking Qualifications Required: - Degree in biological science, pharmacology or other health-related field or prior qualifications or experience in technical communications preferred - Genuine interest in clinical research, medical advancement and drug and biotechnology development highly beneficial as there is room for advancement within the Clinical Trials area in Teckro. - Excellent computer skills