About Teckro

We founded Teckro to simplify and modernize clinical trials. In fact, thousands of clinical trial investigators and research site staff rely on Teckro to make the most informed decisions for their patients.

That’s where you come in. We’re offering you a role with purpose. Your contribution at Teckro will lead to faster, safer and more efficient clinical trials. Quality of life will be improved. In the end, lives will be saved.

Could you be our newest Teckronaut?

What you’ll Do:

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
Successfully complete the ‘In-House Clinical Trial Training Programme’ delivered by a Senior CRS, covering all aspects of Clinical Trials, including but not limited to: trial design, trial procedures, ICH-GCP, clinical trial regulations, operational activities, safety reporting, monitoring etc. The CRS Level 2 will be deemed competent by both the Senior CRS and CRS Manager.
Undertake other duties in-line with your role and business requirements as required

Multilingual CRS:

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

The Ideal candidate will have:

Japanese speaker, with the ability to communicate fluently; including reading, writing, listening and speaking.
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.
Superb editorial skills with a keen eye for text and graphic layouts
Strong critical thinking and problem solving skills
Strong multi-tasking and time management skills including the ability to effectively prioritise tasks, depending on timelines and demands
Strong interpersonal, verbal and written communication skills
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
Passion for creative solutions, innovation, and divergent thinking
Demonstrated ability to work well as part of a team
Where a candidate is carry out duties in a specific language, proven spoken and written fluency is essential

Qualifications Required:

At least 18+ months relevant experience with proven competencies in the role.
Degree in biological science, pharmacy, pharmacology, other health-related field or prior qualifications or experience in technical communications preferred
Excellent computer skills

Location and Travel:
(Dublin)

Hybrid role - Dublin City Centre, Ireland.
Our Dublin City Centre offices are located less than 3 mins for Pearse St Dart Station and beside the Alex Hotel, making it accessible for all major transport. 
We also offer flexible start/ end times, allowing your schedule to suit your lifestyle
Note: Regrettably we cannot offer work permit sponsorship for this role .To be considered, you must currently be based in Ireland and already hold the necessary legal permissions to work here.

Teckro Benefits:

25 days holidays
Pension
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

We are always looking for amazing people to join our growing team. If you are curious, passionate and motivated, then we want to talk to you!

By submitting your application, you agree that Teckro may collect your personal data for recruiting and related purposes. Teckro's Recruitment Privacy Statement explains what personal information Teckro may process, where Teckro may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Teckro’s use of your personal information.

Clinical Research Specialist - Level 2 (Japanese Speaking)

Benefits

Job Description