ICON plc Logo

ICON plc

Senior Clinical Research Associate

Reposted One Month Ago
Be an Early Applicant
In-Office or Remote
Hiring Remotely in United States of America
Senior level
In-Office or Remote
Hiring Remotely in United States of America
Senior level
Monitor and manage clinical trial sites including qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; perform data review and query resolution; collaborate with investigators and site staff; contribute to study documentation and clinical study reports.
The summary above was generated by AI
Senior CRA/ CRA II

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 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-ZH1

#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

ICON plc New York, New York, USA Office

New York, United States, 0

ICON plc Newark, New Jersey, USA Office

Newark, United States

ICON plc Yardley, Pennsylvania, USA Office

Yardley, United States

Similar Jobs

2 Days Ago
Remote
US
Senior level
Senior level
Healthtech
Independently monitors clinical trial sites through qualification, initiation, interim monitoring, and close-out. Ensures protocol, FDA, ICH-GCP, and SOP compliance; maintains audit-ready site files and Trial Master File documentation; manages investigational product accountability, queries, action items, data transmission, and site communications. Provides site training, completes monitoring reports, and supports junior CRA mentoring. Requires extensive domestic travel, independent contractor status, and strong clinical research expertise.
Top Skills: Electronic Crf PlatformsFda RegulationsIch-Gcp GuidelinesTrial Master File Systems
2 Days Ago
Remote
US
Senior level
Senior level
Healthtech
Independently monitors clinical trial sites through qualification, initiation, interim, and close-out visits. Ensures protocol, FDA, ICH-GCP, and SOP compliance; manages site documentation, investigational product accountability, queries, action items, training, and monitoring reports. Serves as the primary site contact, maintains audit-ready files, and supports database lock activities. Requires extensive domestic travel and independent contractor status.
Top Skills: Electronic Crf PlatformsFda RegulationsIch GcpTrial Master File Systems
2 Days Ago
Remote
United States
Senior level
Senior level
Pharmaceutical
Conducts qualification, initiation, monitoring, and termination visits for clinical trial sites. Manages site quality, performance, regulatory documentation, data integrity, investigational product accountability, enrollment support, and compliance with protocols, Good Clinical Practice, SOPs, and regulations. Serves as the primary contact for investigators and site teams, resolving issues and safeguarding participant safety across oncology, ophthalmology, metabolic, hematology, or CAR-T studies.
Top Skills: Clinical Trial Management SystemElectronic Document Management SystemExcelMS OfficeMicrosoft Word

What you need to know about the NYC Tech Scene

As the undisputed financial capital of the world, New York City is an epicenter of startup funding activity. The city has a thriving fintech scene and is a major player in verticals ranging from AI to biotech, cybersecurity and digital media. It also has universities like NYU, Columbia and Cornell Tech attracting students and researchers from across the globe, providing the ecosystem with a constant influx of world-class talent. And its East Coast location and three international airports make it a perfect spot for European companies establishing a foothold in the United States.

Key Facts About NYC Tech

  • Number of Tech Workers: 549,200; 6% of overall workforce (2024 CompTIA survey)
  • Major Tech Employers: Capgemini, Bloomberg, IBM, Spotify
  • Key Industries: Artificial intelligence, Fintech
  • Funding Landscape: $25.5 billion in venture capital funding in 2024 (Pitchbook)
  • Notable Investors: Greycroft, Thrive Capital, Union Square Ventures, FirstMark Capital, Tiger Global Management, Tribeca Venture Partners, Insight Partners, Two Sigma Ventures
  • Research Centers and Universities: Columbia University, New York University, Fordham University, CUNY, AI Now Institute, Flatiron Institute, C.N. Yang Institute for Theoretical Physics, NASA Space Radiation Laboratory

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account