ICON plc Logo

ICON plc

Senior Clinical Research Associate

Posted One Month Ago
Be an Early Applicant
In-Office or Remote
4 Locations
111K-138K Annually
Senior level
In-Office or Remote
4 Locations
111K-138K Annually
Senior level
Conduct and oversee clinical study site activities for Phase II–IV dermatology and rare disease trials. Responsibilities include site identification, initiation, monitoring, close-out, regulatory and ethics submissions, documentation, query management, feasibility assessments, cost efficiency, and potential CRA mentoring. Requires strong knowledge of ICH-GCP, medical data review, bilingual German and English communication, and willingness to travel internationally and domestically at least 60% of the time.
The summary above was generated by AI
Senior Clinical Research Associate

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.


As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.


At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.
Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.
As a Clinical Research Associate at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV, ensuring adherence to applicable regulations and principles of ICH-GCP. This position is sponsor dedicated supporting Dermatology & Rare Disease trials.
The role:
• Independent, proactive work to set up and monitor studies, complete reports and maintain documentation
• Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions
• Balancing sponsor generated queries
• Taking responsibility for study cost efficiency
• Preparation and review of study documentation and feasibility studies for new proposals
• Potential to assist in training and mentoring fellow CRAs
You will need:
• 18 months+ of monitoring experience in phase I-III trials as a CRA
• College degree in medicine, science, or equivalent
• Previous monitoring experience in medium-sized studies, including study start-up and close-out
• Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
• Excellent written and verbal communication in German & English
• Ability to work to tight deadlines
• Availability to travel least 60% of the time (international and domestic -fly and drive) and should possess a valid driving license
Benefits of Working in ICON:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.


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 careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.


Salary Range

$110,520.00-$138,150.00

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

Similar Jobs

24 Minutes Ago
In-Office or Remote
Texas, USA
Senior level
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
Manages oncology clinical trial sites through qualification, initiation, monitoring, activation, and close-out. Ensures data integrity, subject safety, inspection readiness, regulatory compliance, and adherence to protocols, GCP, SOPs, and applicable regulations. Reviews risk indicators, resolves issues, develops CAPA plans, supports IRB and regulatory submissions, trains site staff, and maintains site relationships. Requires solid tumor oncology monitoring experience and up to 50% travel.
Top Skills: Veeva Systems
2 Hours Ago
In-Office or Remote
Texas, USA
Senior level
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
Conduct remote and on-site monitoring for oncology clinical trials, ensuring data integrity, patient safety, protocol compliance, inspection readiness, and regulatory adherence. Manage site communications, essential documents, IRB/EC submissions, risk indicators, CAPA plans, training, site activation, feasibility, and close-out activities. Lead site engagement and mentor less experienced CRAs while supporting regulatory inspections.
Top Skills: CapaGood Clinical Practice (Gcp)GxpRisk-Based MonitoringVeeva Systems
17 Hours Ago
Remote
US
106K-141K Annually
Senior level
106K-141K Annually
Senior level
Biotech
Manages and monitors clinical trial sites to ensure patient safety, data quality, protocol compliance, and regulatory adherence. Conducts site visits, tracks enrollment and study data, reconciles serious adverse events, supports audits and inspections, and manages study milestones. Mentors and trains CRAs, develops monitoring tools, reviews reports, assesses site risks, and collaborates with clinical study teams, vendors, and investigative sites. Requires significant clinical operations and CRA monitoring experience, with travel up to 40–60%.
Top Skills: Clinical Data Management SystemsClinical Trial Management Systems (Ctms)Ich-GcpExcelMicrosoft OutlookMicrosoft PowerpointMicrosoft Word

What you need to know about the Los Angeles Tech Scene

Los Angeles is a global leader in entertainment, so it’s no surprise that many of the biggest players in streaming, digital media and game development call the city home. But the city boasts plenty of non-entertainment innovation as well, with tech companies spanning verticals like AI, fintech, e-commerce and biotech. With major universities like Caltech, UCLA, USC and the nearby UC Irvine, the city has a steady supply of top-flight tech and engineering talent — not counting the graduates flocking to Los Angeles from across the world to enjoy its beaches, culture and year-round temperate climate.

Key Facts About Los Angeles Tech

  • Number of Tech Workers: 375,800; 5.5% of overall workforce (2024 CompTIA survey)
  • Major Tech Employers: Snap, Netflix, SpaceX, Disney, Google
  • Key Industries: Artificial intelligence, adtech, media, software, game development
  • Funding Landscape: $11.6 billion in venture capital funding in 2024 (Pitchbook)
  • Notable Investors: Strong Ventures, Fifth Wall, Upfront Ventures, Mucker Capital, Kittyhawk Ventures
  • Research Centers and Universities: California Institute of Technology, UCLA, University of Southern California, UC Irvine, Pepperdine, California Institute for Immunology and Immunotherapy, Center for Quantum Science and Engineering

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account