Senior CRA Job at iconplc (PORTLAND, BLUE BELL, LOS ANGELES, CA, SEATTLE, WA, SAN FRANCISCO, CA)

Senior CRA CRA II

ICON plc is a world-leading healthcare intelligence and clinical research organi...

Location

Netherlands , Utrecht

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Life science degree or equivalent
2+ years (CRA II) or 4+ years (Senior CRA) independent monitoring experience in Phase II–IV trials
Strong knowledge of clinical trial processes and regulatory standards
Excellent communication, organization, and problem-solving skills
Proficiency with clinical trial systems and tools
Fluency in Dutch and English both Spoken and Written
Should possess a valid driver’s license

Job Responsibility

Managing clinical studies in the Netherlands for Small and Medium sized Biotech sponsors, across multiple therapeutic areas
Independently monitor Phase II–IV clinical trials to ensure compliance with ICH-GCP and regulatory requirements
Conduct site qualification, initiation, monitoring, and close-out visits
Manage study documentation, regulatory submissions, and ethics/IRB approvals
Collaborate with cross-functional teams and site staff to ensure high-quality data and patient safety
Mentor and support site personnel and junior CRAs
Ensure study cost efficiency and timely issue resolution

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Fulltime

CRA II / Senior CRA

CRA II / Senior CRA FSP Global Biotech, Home-based in Newcastle or Sydney prefer...

Location

Australia , Sydney or Newcastle

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Bachelor's degree in a scientific or healthcare-related field
Minimum of 2 years of experience as a 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 and should possess a valid driver’s license

Job Responsibility

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

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Senior Clinical Research Associate

ICON plc is seeking an experienced Senior Clinical Research Associate (Senior CR...

Location

United States , Blue Bell

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Bachelor’s degree in a scientific or healthcare-related field
At least 1 year of independent monitoring experience for CRA II consideration and 3 years for Senior CRA
Strong knowledge of clinical trial processes, regulatory requirements, and ICH-GCP guidelines, with a genuine interest in high-quality research
Excellent communication and organizational skills with strong attention to detail
Ability to work both independently and collaboratively while contributing to a positive, fast-paced team environment
Ability to travel approximately 60 percent of the time, both domestically and internationally by air and car, with a valid driver’s license required

Job Responsibility

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

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Fulltime

Senior CRA - Ophthalmology - West Coast

Sr CRA - West coast Ophthalmology. ICON plc is a world-leading healthcare intell...

Location

United States , PORTLAND, BLUE BELL, LOS ANGELES, SEATTLE, SAN FRANCISCO

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

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 on the West coast US
Complex ophthalmology monitoring experience required (retinal disorders, retinal degeneration, macular edema)
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

Job Responsibility

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

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Vp, cuso compliance risk assessment officer

The Compliance Department at Credit Agricole's Combined US Operations (CUSO) see...

Location

United States Of America , NEW YORK

Salary:

130000.00 - 160000.00 USD / Year

Crédit Agricole

Expiration Date

Until further notice

Requirements

Bachelor's degree required
advanced degree preferred
7+ years in compliance within the financial services industry, with at least 2-3 years in a CRA-related role
Strong understanding of US banking regulations applicable to Foreign Banking Organizations (FBOs), including BSA/AML, OFAC sanctions, consumer protection, and prudential requirements
Experience working in a Global Corporate Compliance Risk Assessment Program
Deep knowledge of compliance program frameworks, risk assessment methodologies, and the three lines of defense model
Stakeholder Management and Ability to Influence across the Three Lines of Defense.
General rules and regulations knowledge (FED, OCC, NYDFS, SEC, FINRA,)
Proven ability to manage multiple priorities, coordinate cross-functional initiatives, and meet deadlines in a fast-paced environment
Excellent written and verbal communication skills with the ability to present complex compliance concepts to diverse audiences

Job Responsibility

Support the CRA program by coordinating assessments across all business lines, maintaining the assessment calendar, and ensuring timely completion of all activities.
Enhance CRA methodologies and tools to improve risk identification, analysis, and reporting capabilities.
Monitor action plans resulting from CRAs to ensure timely remediation of identified compliance gaps.
Collaborate with Monitoring & Testing, Internal Controls, and Training teams to ensure CRA results inform their program activities and support the broader compliance framework.
Maintain CRA policies and procedures to reflect current regulatory requirements, industry best practices, and organizational changes
Coordinate with the Paris-based GRC (Governance, Risk, and Compliance) tool development team to implement system enhancements and maintain platform effectiveness.
Prepare management reporting on CRA activities, findings, and trends for senior leadership and governance committees.
Support regulatory engagement during examinations and audits, providing documentation and explanations of the CRA program as needed
Identify emerging compliance risks through ongoing monitoring of regulatory developments, industry trends, and business activities.

Fulltime

Storage EU CRA Program Manager

Provides support and/or lead teams through the Engineering development process a...

Location

United States of America , Fort Collins; Houston

Salary:

111000.00 - 211000.00 USD / Year

Hewlett Packard Enterprise

Expiration Date

March 30, 2026

Requirements

Bachelor's or Master's degree in Business Management, Engineering, Computer Sciences, or equivalent
6-10 years experience in Program Management
PMP/PMI certification preferred
Smartsheet experience required
Experience with security and regulatory compliance initiatives
Experience managing programs that cross organizational boundaries
Extensive experience with using Smartsheet and other program planning tools and software packages to create, manage, and track program results
Excellent analytical and problem-solving skills
Demonstrated business acumen and successful experience managing all aspects of programs, including communicating with stakeholders and directing very large matrixed teams and resources
Excellent written and verbal communication skills

Job Responsibility

Manage and lead the European Union Cyber Resilience Act (EU CRA) program for the Storage Business
Oversee the multiple activities required to meet the EU CRA regulatory requirements, across all Storage product families, within the designated timeframe
Responsible for creating schedules, ensuring alignment and the successful execution of critical deliverables within schedule timeframes
Responsible for managing program budget, resource allocation plan, and other supporting requirements for delivery of the program objectives
Manage the activities of the project teams, internal and external partners to ensures progress against established plan and makes determinations based on analysis of business information to alter or update schedule and resource allocation to meet program requirements and schedule
Communicate program progress, drive escalations, and provide program analysis to product stakeholders
collaborate with management and internal PSO workstreams to recommend and implement changes to schedule, processes, or business plans to resolve escalated issues, produce solutions, ensure adherence to budgets and established program roadmaps and schedules
Drive innovation and the integration of new technologies and initiatives into the program and activities to gain efficiencies and produce results
Will lead and provide guidance and mentoring to less-experienced staff members

What we offer

Health & Wellbeing
Personal & Professional Development
Unconditional Inclusion

Fulltime

Senior Clinical Research Associate

ICON plc is a world-leading healthcare intelligence and clinical research organi...

Location

Bulgaria , Sofia

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

University degree
CRA with a minimum of 3.5 years of independent on-site monitoring experience in a bio/pharma/CRO
Proven Skills in Site Management including management of site performance and patient recruitment
Ability to work occasionally form the sponsor's office in Sofia
Good IT skills
Ability to understand and analyze data/metrics and act appropriately
Capable of managing complex issues, works in a solution-oriented manner.

Job Responsibility

Site management and monitoring activities for assigned applicable Phase I and all Phase II-IV clinical Investigator sites
Conducts remote and onsite visits including but not limited to initiation visits, monitoring visits, close-out visits
Managing Investigator site and site activities and monitoring site data, to ensure patient safety and ethical and regulatory compliance to provide quality data required for global regulatory submissions for approval of drugs.
Managing Investigator sites to ensure the Investigator and Site Staff meet all aspects of study delivery and commitments to make certain the operational study execution is on track from site selection to site close out.
The CRA is responsible for training the Investigator and site staff on these strict regulatory regulations and procedures for timely reporting and as well as ensuring ongoing compliance.
The CRA proactively identifies potential issues and develops site Corrective Actions / Preventive Actions (CAPAs) and ensures timely and sufficient resolution of issues that may impact compliance or quality of study related activities or data.
As key contributor to the Trial Master File and study documents at the country level, ensures essential documents are appropriate and filed in a timely manner in the Investigator Site File.
Contributor in the preparation, conduct and follow up of Site Audits and Regulatory Inspections to ensure a successful outcome.

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Qa/qc Coordinator

Location

Qatar , Doha

Salary:

Not provided

Airswift Sweden

Expiration Date

Until further notice

Requirements

BSc degree or higher in Mechanical or Metallurgical Engineering from a recognized Engineering faculty
Valid CSWIP 3.2.1 or AWS Senior Welding Inspection Certificate (SCWI) with at least five years of post-certification experience
B Gas Grade 2 or NACE Level II Coating Inspector qualification is preferable
NDT Level II in RT, UT, PT & MT / NDT qualifications per ASNT or ISO requirements
Certified QMS Lead Auditor in accordance with ISO 9001:2015 with at least five years of auditing experience
Strong knowledge of international codes/standards: EN, ISO, API, ASME, ASTM
Good leadership and communication skills
Ability to work on projects in a complex, multicultural environment
Proficient in MS Office, database management, spreadsheets, and email communication
Minimum 15 years as QA/QC Coordinator or QA/QC Lead, leading multidiscipline QC inspector teams for inspection and testing activities on major oil and gas projects, including offshore process platforms, jackets, subsea pipelines, and all phases of manufacturing, fabrication, construction, and offshore installation

Job Responsibility

Report quality status daily to the Senior Quality Engineer
Supervise and coordinate all activities related to the Quality Management System during construction and installation phases
Ensure all works by contractors, subcontractors, vendors, manufacturers, service providers, and third-party inspectors comply with project specifications, corporate standards, international codes, and QA/QC requirements
Review technical and quality documents, ITPs, and QA/QC procedures in the document management system
Ensure approved QA/QC documents are implemented at worksite level, including quality plans, control procedures, ITPs, and inspection checklists
Lead and coordinate QC inspectors’ activities at fabrication sites, construction sites, and offshore installations
review inspection reports
Monitor contractor/vendor implementation of approved quality requirements and address deficiencies
Act as focal point for resolving shop/site-related quality control issues in consultation with senior quality management
Control and follow up on technical deviations, material substitutions, and changes to inspection/test requirements

Senior CRA

iconplc

Location:
United States , PORTLAND, BLUE BELL, LOS ANGELES, CA, SEATTLE, WA, SAN FRANCISCO, CA

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
March 12, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Senior CRA

Senior CRA CRA II

CRA II / Senior CRA

Senior Clinical Research Associate

Senior CRA - Ophthalmology - West Coast

Vp, cuso compliance risk assessment officer

Storage EU CRA Program Manager

Senior Clinical Research Associate

Qa/qc Coordinator

Senior CRA

iconplc

Location:United States , PORTLAND, BLUE BELL, LOS ANGELES, CA, SEATTLE, WA, SAN FRANCISCO, CA

Category:Research and Development

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:March 12, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Senior CRA

Senior CRA CRA II

CRA II / Senior CRA

Senior Clinical Research Associate

Senior CRA - Ophthalmology - West Coast

Vp, cuso compliance risk assessment officer

Storage EU CRA Program Manager

Senior Clinical Research Associate

Qa/qc Coordinator

Location:
United States , PORTLAND, BLUE BELL, LOS ANGELES, CA, SEATTLE, WA, SAN FRANCISCO, CA

Category:
Research and Development

Contract Type:
Not provided

Job Posted:
March 12, 2026