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Scientific Affairs Specialist II

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ICON plc

Aug 22, 2024

  • Job
    Full-time
    Mid Level
  • Science
    Research & Development
  • Dublin
  • Quick Apply

AI generated summary

  • You should have a Bachelor’s in Medical Technology/Life Sciences, 3+ years of experience, GCP certification, clinical lab knowledge, and proficiency in MS Word/Excel.
  • You will manage test road maps, monitor assay releases and clinical trends, generate data for test solutions, handle RFI queries, improve data quality, and assist with marketing activities.

Requirements

  • Bachelor's or above degree in Medical Technology/ Life Sciences or equivalent
  • Minimum of 3 years of relevant experience.
  • Knowledge of clinical laboratory concepts and terminology.
  • Proficiency in MS Word and Excel.
  • GCP Certification.
  • Customer-focused mindset with the ability to provide timely, confident, reliable, and friendly service to internal and external customers.
  • This position is based at our Dublin office at least three days/week.

Responsibilities

  • Test menu road map mgmt.
  • Monitor new assay release from diagnostic vendors
  • Monitor trends in new clinical trial therapeutic areas and associated assays/tools
  • Generate objective data that identifies needed test solutions and contribute to establishment of those solutions
  • Manage scientific component of RFI queries
  • Triage SA queries and perform data investigations that improve clinical trial data quality
  • Assistance with Marketing activities, including, creation of standard SA slides and Creation of case studies for abstract/webinar/white paper based on completed studies

FAQs

What is the primary role of a Scientific Affairs Specialist II at ICON?

The primary role is to deliver consistent and high-quality scientific support for global clinical studies, including researching diagnostic assay solutions, providing test menu recommendations, investigating data queries, and assisting in the creation of scientific communications.

What qualifications are required for this position?

Candidates must have a Bachelor's or higher degree in Medical Technology or Life Sciences, a minimum of 3 years of relevant experience, knowledge of clinical laboratory concepts, proficiency in MS Word and Excel, and GCP Certification.

Where is this position based?

This position is based at the Dublin office, and the employee is required to be present at least three days a week.

What type of experience is preferred for applicants?

A minimum of 3 years of relevant experience in a scientific or clinical laboratory setting is preferred.

What kind of tasks will I be involved in if I get this job?

Tasks include managing the test menu roadmap, handling scientific components of RFI queries, triaging queries to improve clinical trial data quality, and assisting with marketing activities such as creating presentations and case studies.

Is there an opportunity for career growth in this position?

Yes, ICON values high performance and nurtures talent, providing opportunities for career growth and development within the organization.

Are there additional benefits offered beyond salary?

Yes, ICON offers a range of benefits including various annual leave entitlements, health insurance options, retirement planning, a global Employee Assistance Programme, life assurance, and flexible optional benefits.

Is ICON an equal opportunity employer?

Yes, ICON is committed to providing a workplace free of discrimination and harassment, ensuring all qualified applicants receive equal consideration for employment.

What is the expected workload for this position?

The role is expected to involve a significant commitment in managing scientific affairs related to clinical trials, requiring attention to detail and the ability to handle multiple tasks efficiently.

How does ICON support employee well-being?

ICON offers various well-being and work-life balance opportunities, including access to health resources, employee assistance programs, and additional flexible benefits to cater to employees' and their families' needs.

Science & Healthcare
Industry
10,001+
Employees

Mission & Purpose

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.