ICON plc

Senior CRA

ICON plc$110K — $138K *
US-Anywhere
+ 4 other locationsRemote
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Advanced degree in life sciences, nursing, or medicine required.
  • Extensive Clinical Research Associate experience with knowledge of trial processes and regulations.
  • Strong organizational and problem-solving skills to manage multiple sites and projects.
  • Expertise in monitoring practices and data integrity with proficiency in clinical trial software.
  • Excellent communication and interpersonal skills with stakeholder management experience.
  • Located in the MidAtlantic area of the US is mandatory.
  • Oncology monitoring experience is essential.
  • Willingness to travel at least 60% of the time with a valid driver’s license.

Responsibilities

  • Monitor clinical trial sites for compliance with study protocols and GCP standards.
  • Conduct site visits to evaluate performance and address issues for trial execution.
  • Collaborate with teams for timely data collection and reporting accuracy.
  • Provide training and support to site staff and CRAs for high trial conduct standards.
  • Build and maintain relationships with site personnel and stakeholders to ensure smooth operations.

Benefits

  • Comprehensive total rewards package for health and career support.
  • Health programmes including medical, dental, and vision coverage.
  • Retirement and pension plans for financial security.
  • Life assurance and disability coverage.
  • Employee assistance programmes for wellbeing.
  • Learning and development opportunities through structured training.
Full Job Description
Senior CRA - Oncology - MidAtlantic

What You Will Be Doing:

  • 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:

  • Advanced degree in a relevant field such as life sciences, nursing, or medicine.

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

  • 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.

  • Must be located in the MidAtlanyic area of the US

  • Oncology monitoring experience is required

  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license


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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