Clinical Research Specialist

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, analyse, 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
• 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.

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