CRA II Job at iconplc

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

Clinical Research Associate II / Senior CRA

We are currently seeking a Senior Clinical Research Associate (CRA) to join our ...

Location

Germany , Mannheim

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
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

Clinical Research Associate II / Senior CRA

We are currently seeking a Senior Clinical Research Associate (CRA) to join our ...

Location

Germany , Mannheim

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
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

Parttime

Clinical Research Associate II / Senior CRA

CRA II/Senior CRA Home based Germany. ICON plc is a world-leading healthcare int...

Location

Germany , Mannheim

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
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

Clinical Research Associate II

Clinical Research Associate II - France - Remote. ICON plc is a world-leading he...

Location

France , Paris

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Minimum 24 months' experience as a CRA within the pharmaceutical industry or a CRO
Excellent organization skills
Ability to work well in a dynamic environment and able to prioritize and respond to changing needs of the business
Strong IT skills
Strong communication with the ability to multitask and work effectively under pressure
Fluency in French and professional proficiency in English

Job Responsibility

Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out
Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan
Developing effective relationships with investigator site staff to ensure that key clinical metrics are met
Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues
Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines

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

Payroll specialist - hr analyst ii

We are seeking a highly analytical and detail-oriented HR Analyst II to join our...

Location

Canada , Toronto

Salary:

27.62 CAD / Hour

Randstad

Expiration Date

May 18, 2026

Requirements

Expat Experience: Minimum of 3 years of experience managing expatriate or shadow payrolls
Regulatory Knowledge: Strong working knowledge of Canadian Federal/Provincial and U.S. regulatory requirements (CRA, Revenue Québec, and IRS)
System Proficiency: Working knowledge of Workday (specifically reporting and year-end processes)
Technical Skills: Advanced Excel skills for report reconciliation and data analysis
Analytical Ability: Strong analytical skills with a focus on report reconciliation principles and high attention to detail
Overall Experience: 3-4 years of relevant experience in a large corporate environment

Job Responsibility

Tax Compliance & Year-End Processing
Government Filings: Balance all year-end tax slips and complete federal and provincial government filings accurately and on time
Audit Support: Participate in internal and external payroll audits, providing necessary documentation and reconciliations
Data Integrity: Run and action PIER/Variance reports to correct data errors and validate the accuracy of annual reports from the CRA and Revenu Québec
Manual Adjustments: Prepare manual and amended tax slips and support payroll accounting to ensure year-end data is recorded accurately
Expatriate & Executive Payroll
Global Mobility: Manage daily administrative functions for expatriate shadow payrolls and support globally mobile employees
Executive Support: Provide customized payroll and year-end tax slip support for the CEO and Senior Executive Team
Board of Directors: Manage the end-to-end payroll process for the Board of Directors, including processing quarterly Director Fees
System & Process Management

What we offer

High-Profile Exposure: Gain experience supporting C-suite executives and the Board of Directors
Specialized Expertise: Deepen your knowledge of complex cross-border tax and global mobility payroll
Collaborative Environment: Work within a tight-knit team of 6 professionals with a culture of excellence
Career Growth: Potential for contract extension or permanent conversion based on performance and business needs
Professional Training: Benefit from a structured 2-week training period to ensure your success in the role

Fulltime

CRA II

iconplc

Location:
United States

Category:
IT - Administration

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
April 22, 2026

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Job Posted:April 22, 2026

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