Find Senior clinical data Jobs in Tallaght County Dublin

Clinical Research Specialist - Level 2 - (6 Month Fixed Term Contract)
Teckro Limited —Dublin, County Dublin
- Full-time
- Hybrid work
- Nursing
- Hotel
- Analysis skills
- Gym membership
- Life insurance
Quick apply
2h
Client Partner, Strategy Consulting Large Pharma Advisory, 1 year contract
IQVIA —Dublin, County Dublin
- Full-time
- Sales
- Organisational skills
- Communication skills
7d
Senior Speech and Language Therapist
Beacon Hospital —Dublin, County Dublin
- Full-time
Quick apply
14d
Assistant Director of Nursing – Theatre Department
Blackrock Health Hermitage Clinic —Lucan, County Dublin
- Full-time
- Management
- Clinic
- No degree
- Employee assistance program
Quick apply
14h
Clinical Governance Administrator
Medica —Dublin, County Dublin
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Administrative experience
Quick apply
Enterprise Applications COE Director
Uniphar PLC —DUBLIN 24, County Dublin
- Full-time
- Azure
- DevOps
- ERP systems
Quick apply

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Clinical Research Specialist - Level 2 - (6 Month Fixed Term Contract)

Teckro Limited -
Dublin, County Dublin

Quick apply

Job details

Full-time
2 hours ago

Benefits

Tax Saver Scheme
Bike to work scheme
Gym membership
Life insurance

Qualifications

Nursing
Analysis skills
Computer skills
Communication skills

Full job description

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
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.

Quick apply

Refine Your Search

senior clinical data jobs in tallaght county dublin

Clinical Research Specialist - Level 2 - (6 Month Fixed Term Contract)

Client Partner, Strategy Consulting Large Pharma Advisory, 1 year contract

Senior Speech and Language Therapist

Assistant Director of Nursing – Theatre Department

Clinical Governance Administrator

Enterprise Applications COE Director

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