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?

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

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

• 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