ICON plc

Senior Research Scientist

ICON plc$110K — $130K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Minimum 6 years of experience in genomic assays
  • PhD in a science-related field preferred; bachelor’s or master’s with 6-8 years of experience considered
  • Experience with medical device design or manufacturing according to ISO 13485 standards preferred
  • Strong interpersonal, communication, and organizational skills
  • Ability to multitask and lead teams while demonstrating creative problem-solving capabilities

Responsibilities

  • Independently direct the development and validation of new genomic assays
  • Lead testing of clinical trial samples for RT-PCR, qPCR, and ddPCR assays
  • Manage all aspects of R&D assay validations including experiments and data analysis
  • Provide updates to sponsors and collaborate with various internal teams like Scientific Affairs and IT
  • Attend and present results in client-facing meetings
  • Maintain high-quality work under pressure while handling multiple projects

Benefits

  • Competitive base salary and performance-related incentives
  • Comprehensive health and wellbeing programs including medical, dental, and vision coverage
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programs and wellbeing resources
  • Learning and development opportunities through structured training
Full Job Description
Senior Research Scientist- onsite- Portland OR

Senior Research Scientist

This is an On-Site role located in Portland, OR

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. The primary role of the Senior Research Scientist is to oversee the scientific aspects of an assay development/validation project. Experience with medical device design manufacturing following ISO 13485 standards preferred.

  • Independently direct development and validation of new genomic assays
  • Exhibit scientific leadership related to the testing of clinical trial samples for RT-PCR, qPCR, and ddPCR assays
  • Independently manage all aspects of R&D assay validations; experiments, data analysis, sponsor updates, interact with: Scientific Affairs, IT, operational labs, business development, and project management teams
  • Experienced multi-tasker with the ability to work independently with a high degree of quality
  • Attend and present results at client facing meetings
  • Excellent oral and written communication skills
  • Proven track record in delivering focused customer service and client satisfaction
  • Experience in managing multiple projects and meeting deadlines
  • Excellent presentation skills
  • Serve as a scientific leader within the department
  • Ability to remain composed and even keeled in stressful situations, performing effectively in spite of shifting priorities, workload and external pressures
  • Knowledge of basic computer programs


To be successful in this role, you will have:

  • Minimum 6 years of experience in genomic assays
  • PhD in science related field preferred, Bachelors or master's with 6 to 8 years of experience
  • Experience with medical device design or manufacturing following ISO 13485 standards preferred.
  • Strong interpersonal and communication skills, good laboratory, and organizational skills, including the ability to work independently and efficiently.
  • Ability to multitask, along with an orientation toward teamwork and leadership, and strong creative thinking and problem-solving skills.

#LI-FL-1

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways


Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Are you a current ICON Employee? Please click here to apply

About ICON plc

ICON plc is a global provider of drug development and commercialisation services to the pharmaceutical, biotechnology and medical device industries. The company specialises in the strategic development, management and analysis of programs that support clinical development. ICON has approximately 15700 employees in 40 countries. The company was founded in Dublin, Ireland in 1990 and is headquartered in Leopardstown, Dublin. ICON has been publicly traded on the NASDAQ since 1998.
Learn more about ICON plc
Size
39,300 employees
Market Cap
$16.2 billion
Industry
Net Income
$332.3 million
Founded
2017
5 Year Trend
+26.9%
Revenue
$2.7 billion
NASDAQ

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