Medical Research Associate conducting clinical assessments and phlebotomy at ICON. Responsible for ensuring volunteer health and comfort during trials in a research environment.
About the role
- Clinical Research Specialist at Teckro improving clinical trial efficiency through scientific information analysis and project management.
Responsibilities
- Analyse, understand, and process complex scientific/medical/pharmaceutical information
- Working closely with the Senior CRS, execute the layout and structure of clinical information required to utilize our products efficiently and effectively
- Involved in the assessment of client documents prior to project development to determine project timelines
- Work with internal project teams and study team timelines to ensure timely delivery of high-quality solutions
- Assisting with the updating of clinical operations process guides
- Responsible for quality checking projects as part of risk assessment
- Contribute to process and product updates, working closely with other Teckro teams such as software and the product team
- Communicate effectively within the team and also across other Teckro teams regularly
- Responsible for the training, mentoring and development of CRS level 1, including the preparation and development of training materials and tools
- Undertake other duties in-line with your role and business requirements as required
- Assist with translation tasks across various departments within the company
- To perform study demos of Teckro, to join Investigator’s Meetings (IMs) and to provide training in local languages to study teams and/or relevant users
Requirements
- Japanese speaker, with the ability to communicate fluently; including reading, writing, listening and speaking
- Degree in biological science, nursing, or other health-related field
- Some clinical trials experience, preferably in the clinical operations setting of clinical trials, understanding the day to day needs, risks and blockers of clinical trial teams
- A good understanding of ICH / GCP and essential clinical trial documents
- 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
- Excellent communication skills
Benefits
- 25 days holidays, entitlement increases with length of service
- Pension, available immediately upon joining Teckro
- Healthcare
- Life Insurance
- Share Options
- 50% Maternity leave pay after capped length of service
- Paid Paternity leave scheme
- Bike to Work/ Tax Saver Scheme
- Gym/Wellness Allowance
- Sports and Social Club
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Tech skills
Location requirements
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