Clinical Research Specialist(Level 2) (12 Month Contract)

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:

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

The Ideal candidate will have:

Demonstrate superb communication skills

Ability to work autonomously as well as part of the team

Excellent 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

Exceptional analytical and logical skills with highly developed critical thinking, problem-solving and decision-making skills

Passion for creative solutions, innovation, and divergent thinking

Qualifications Required:

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

Location and Travel:

(Dublin)

Hybrid role currently this is set to 2-3 days per week onsite - 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, entitlement increases with length of service

Pension, available immediately upon joining Teckro

Healthcare

Life Insurance

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!

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