Early - career Policy Research Analyst supporting science, technology, and innovation policy research at SRI. Working collaboratively in a hybrid environment to deliver insights and analysis.
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
Clinical Research Specialist responsible for analyzing complex biomedical information and mentoring junior staff in clinical operations for Teckro. Ensuring timely delivery of clinical trial solutions while working in a hybrid model.
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