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