Senior CRA Job at iconplc (Indianapolis)

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

New

Senior CRA - Ph 1/2

A clinical-stage biotechnology organization is seeking an experienced Senior CRA...

Location

United States

Salary:

75.00 - 90.00 USD / Hour

Solomon Page

Expiration Date

Until further notice

Requirements

Bachelor’s degree in life sciences or related discipline
4+ years of In House CRA experience within a sponsor or biotech environment
Experience supporting global clinical trials
Phase I/II trial experience required
Demonstrated experience in site oversight and vendor management
Experience contributing to clinical study management activities

Job Responsibility

Support the Global Clinical Study Lead/Senior Clinical Trial Manager in the operational management of Phase I/II trials from study start-up through close
Provide oversight of CRO monitoring activities, ensuring quality and adherence to protocol and GCP
Act as a key point of escalation for site-related operational issues
Contribute to protocol development, study design discussions, and operational feasibility
Manage operational aspects of investigative site relationships and study execution
Oversee external vendors (IRT, eCOA, cardiac safety, patient reimbursement, etc.) and support vendor performance management
Participate in vendor selection activities, including RFP review and bid defenses
Support development and maintenance of study timelines, operational plans, and budgets
Contribute to development of key study documents and site-facing materials
Support CRF design, UAT, edit check review, and data quality oversight

What we offer

medical
dental
401(k)
direct deposit
commuter benefits

New

Senior CRA - Ph 2/3

A growing biotechnology organization is seeking an experienced Senior CRA to sup...

Location

United States

Salary:

75.00 - 90.00 USD / Hour

Solomon Page

Expiration Date

Until further notice

Requirements

Bachelor’s degree in life sciences or related discipline
4+ years of in-house CRA experience within a sponsor or biotech environment
Experience supporting global clinical trials
Phase II/III trial experience required
Demonstrated experience in site oversight and vendor management
Experience contributing to clinical study management activities

Job Responsibility

Support the Global Clinical Study Lead / Senior Clinical Trial Manager in the operational management of Phase II/III trials from study start-up through closeout
Provide oversight of CRO monitoring activities, ensuring quality, protocol compliance, and GCP adherence
Act as a key point of escalation for site-related operational issues
Contribute to protocol development, study design discussions, and operational feasibility
Manage operational aspects of investigative site relationships and study execution
Oversee external vendors (IRT, eCOA, cardiac safety, patient reimbursement, etc.) and support vendor performance management
Participate in vendor selection activities, including RFP review and bid defenses
Support development and maintenance of study timelines, operational plans, and budgets
Contribute to the development of key study documents and site-facing materials
Support CRF design, UAT, edit check review, and data quality oversight

What we offer

medical
dental
401(k)
direct deposit
commuter benefits

New

Senior CRA

Sr CRA - West coast oncology; ICON plc is a world-leading healthcare intelligenc...

Location

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

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
Experience monitoring oncology studies 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

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

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

Senior CRA

iconplc

Location:
United States , Indianapolis ▼
Chicago

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
March 19, 2026

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