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