ICON plc Logo

ICON plc

Senior Clinical Research Associate

Posted 25 Days Ago
Be an Early Applicant
Remote
Hiring Remotely in United States of America
Senior level
Remote
Hiring Remotely in United States of America
Senior level
Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; review and resolve data queries; and contribute to protocols and clinical study reports. The role requires extensive travel, independent monitoring experience, strong clinical research knowledge, and familiarity with ICH-GCP guidelines.
The summary above was generated by AI
Senior CRA - Home-Based (US)

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


We are currently seeking a Senior Clinical Research Associate or Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.


What you will be doing

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff to facilitate smooth study conduct.
  • Performing data review and resolution of queries to maintain high-quality clinical data.
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your profile

  • Bachelor's degree, or its international equivalent in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role
  • Minimum of 1 year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate.
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
  • Strong organizational and communication skills, with attention to detail.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

#LI-KC2 #LI-REMOTE


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.

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

Similar Jobs

2 Days Ago
Remote
USA
109K-202K Annually
Senior level
109K-202K Annually
Senior level
Biotech • Pharmaceutical
Manages clinical trial sites for Phase I–IV studies through on-site and remote monitoring. Ensures compliance with ICH/GCP, regulations, protocols, and company procedures; oversees recruitment, data integrity, patient safety, site performance, risk resolution, documentation, and corrective actions. Serves as the primary site contact, supports audits and inspections, trains site personnel, collaborates with cross-functional teams, and contributes to efficient, high-quality trial execution. Requires 80% travel across the western United States.
Top Skills: Clinical Trial Management Systems (Ctms)Emea RegulationsFda RegulationsIch/Gcp
3 Days Ago
Remote
Florida, USA
Senior level
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
Conducts site selection, initiation, monitoring, and close-out visits for sponsor clinical trials. Ensures ICH-GCP, regulatory, documentation, patient safety, training, drug accountability, recruitment, data quality, and payment compliance. Serves as the primary site-sponsor contact, resolves data queries, tracks site progress, escalates risks, and collaborates with clinical operations partners. Requires extensive regional travel across the Southeast.
Top Skills: CtmsEtmfIch-Gcp
4 Days Ago
In-Office or Remote
125K-142K Annually
Senior level
125K-142K Annually
Senior level
Biotech
Conducts clinical trial site monitoring and management for ophthalmology or oncology studies, including pre-study, initiation, routine monitoring, and close-out visits. Ensures protocol compliance, informed consent, patient safety, data integrity, SAE reporting, CRF review, query resolution, registry management, and regulatory adherence. Coordinates with vendors, study teams, and clients; supports employee training and may coordinate local clinical projects. Requires frequent site travel and adaptability in a fast-paced, technology-based environment.
Top Skills: Case Report Forms (Crfs)Clinical Data Management SystemsElectronic Data Capture Systems

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