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?
Expectations include the ability to build relationships (internally and externally), identify client needs, deliver our strategic and innovative solutions, and ensure that client contracts are delivered on time and on budget. A program director is responsible for ensuring a superior client experience and driving account growth.
This experienced professional exhibits decision quality, action orientation, communication savvy, and resourcefulness to meet both Teckro and client needs.
What you’ll Do:
- 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
- Undertake other duties in-line with your role expertise and business requirements as required
The Ideal candidate will have:
- 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
- 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:
- Degree in biological science, nursing, pharmacology, 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
Location and Travel:
(Dublin/Limerick)
Hybrid work option with the flexibility to work in our Irish offices located in Dublin or Limerick City. Currently this is set to 3 days per week onsite.
We also offer flexible start/ end times, allowing your schedule to suit your lifestyle
Willingness to travel internationally as required
Please note: Regrettably we cannot offer work permit/sponsorship or self-sponsorship for this role. Eligible applicants must already hold valid and legal work permit for Ireland
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.
