ICON plc

Senior Clinical Research Associate

ICON plc$110K — $138K *
US-Anywhere
+ 4 other locationsRemote
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes
  • 3 years of monitoring clinical trials including oncology
  • At least 1 year of oncology monitoring experience
  • Experience with Phase I/II solid tumors, particularly gastro, colorectal, breast, and head and neck
  • Proven ability to manage multiple sites and projects simultaneously
  • Excellent communication and interpersonal skills, able to influence compliance

Responsibilities

  • Monitor clinical trial sites to ensure protocol and regulatory adherence
  • Conduct site visits to assess performance and resolve issues
  • Collaborate with cross-functional teams for timely data collection
  • Provide training and guidance to site staff and other CRAs
  • Build and maintain effective relationships with site personnel

Benefits

  • Competitive base salary and performance-related incentives
  • 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 Clinical Research Associate - Oncology - East Coast

Senior Clinical Research Associate - Oncology - East Region

What You Will Do:

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.

Key responsibilities include:

  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.

  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.

  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.

  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.

  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.

Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field

  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.

  • 3 years of monitoring clinical trials

  • Atleast 1 year of oncology monitoring experience

  • Phase I/II solid tumor: gastro, colorectal, breast, head and neck experience highly preferred.

  • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.

  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.

  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.

  • Located on the East coast near major hub.

  • Willingness to travel as required (approximately 60%)


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


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 to read more about the benefits ICON offers.

Salary Range

$110,520.00-$138,150.00

Are you a current ICON Employee? Please click 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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