Senior 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
Act as a clinical trial advisor and subject matter expert, providing clinical oversight on a multidisciplinary team, to ensure timely delivery of high quality solutions.
Review study protocols/documents to identify areas of vulnerability and operational importance; customize the platform to meet the requirements of individual studies.
Review projects from an End Users perspective to ensure quality, accuracy and relevance before being deployed to the client.
Review/analyze program/study-level risk registers/RACTs to assist in defining 'Engage' messaging campaigns or other use cases for the Teckro platform in order to help client study teams meet study objectives and minimize study risks.
Present findings/suggestions to client study teams with support from Project Manager and/or Program Lead/Director for assigned account.
Monitor/analyze platform searches: identification of trends and unanticipated key variables; provide data to the development teams for product improvements.
Act as a clinical trials resource for the Product team: assisting with testing new functions and providing insight into the day to day work of a clinical research professional.
Contribute to maintaining and improving in-house templates, SOPs and guides.
Where required, assist in the training of CRS Level 2 team members to CRS duties, giving in-depth knowledge of what is expected at Level 3.
Where required, assist in the training and upskilling of CRS Level 3 team members, by mentoring and allowing shadowing of projects and duties.
Shadowing Level 3 team members as they conduct CRS duties on projects.
Assist in the induction, training and upskilling of team members, when required.
Undertake other duties in-line with your role and business requirements as required.
Regularly contribute ideas for innovation and product, quality and process improvements and additions.
The Ideal candidate will have
Minimum 3 years of clinical operations/clinical research experience within a hospital or CRO setting (study coordinator, research nurse, CRA/study monitor) or at least 18+ months relevant Teckro CRS Level 3 experience, with proven competencies in the role.
In depth knowledge of global drug development, clinical trial processes, ICH-GCP, regulations and documentation.
Broad clinical research experience from working within a variety of therapeutic areas preferred.
Keen interest in technology solutions and Software as a Service (SaaS).
Experience with clinical operations/industry-related technology solutions and a keen ability to learn new software.
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.
Ability to work both independently and in a team-orientated, collaborative environment – able to get the work done, with minimal or no supervision.
Strong interpersonal, verbal and written communication skills.
Results and performance driven.
Adaptable and flexible.
If duties are carried out in a specific language, proven spoken and written fluency is essential.
Qualifications Required
Degree in biological science, nursing, pharmacy or other health-related discipline.
Post graduate qualification in Clinical Research preferred.
Proven competencies with Clinical Research methodologies and day to day activities.
Location and Travel
(Dublin)
Hybrid role - Dublin City Centre, Ireland.
Our Dublin City Centre offices are located less than 3 mins from 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: 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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