CRA II / Senior CRA Job at iconplc (Sydney or Newcastle)

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

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 Clinical Research Associate II - FSP

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

Turkey

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
Monitoring Experience: Minimum 5 years relevant experience in clinical research site monitoring (preferably 3 years in Oncology)
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Global clinical trial experience
Must be fluent in English and in the native language(s) of the country they will work in
Significant travel (60-80%) within area is required. May require some international travel and some weekend travel
Valid driver’s license and passport required
Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
Demonstrated knowledge of global and local regulatory requirements
Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)

Job Responsibility

Oversight of Monitoring Responsibilities and Study Conduct
Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and client standards to achieve project goals, timelines and quality
Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
During study conduct, serve as the primary point of contact for assigned investigator sites. Work in partnership with and/or escalate to the SCP to ensure quality of site delivery
Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients
provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks
Attend investigator meeting when required (virtual or F2F). Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators. Partner with SCP and the study team to define and support recruitment initiatives at site level
Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities and ensure these are conducted accordance to the SMP, Standard Operating Procedures (SOPs) and commensurate with emerging issues and technologies
Monitor site level adverse events (AEs) and serious adverse events (SAEs) and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution

What we offer

Flexible work arrangements
Career growth and development
Supportive and inclusive environment
Diverse therapeutic areas and project exposure
Advanced Technology

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

New

Senior Clinical Research Associate

Senior CRA - (Bangalore - Office‑Based, Phase IV / PMS / RWE Studies). ICON plc ...

Location

India , Bangalore

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

5+ years of experience in clinical research
2–3 years of CRA/monitoring experience, preferably involving Phase II–IV studies
Prior experience in PMS, RWE, or post‑marketing studies is essential
Strong administrative and documentation skills
Experience working with CROs, external vendors, and cross‑functional medical teams
Excellent communication, coordination, and stakeholder‑management skills
Ability to independently handle multiple studies simultaneously

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

Senior Clinical Research Associate

Clinical Research Associate ( CRAII or Senior CRA) - Remote - Romania. ICON plc ...

Location

Romania , Bucharest

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Bachelor’s Degree (or equivalent)
Minimum 3.5 years of independent on-site monitoring experience/experience as a field CRA
Ability to travel with overnight stays
Experience conducting all types of MVs such as: Site Selection, Initiation, Routine Monitoring and Close Out Visits both remotely and on-site
A demonstrated working knowledge of ICH/GCP Guidelines
Excellent record-keeping skills and attention to detail
Fluent in English and Romanian, both written and oral
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

Monitor multiple Phase I, II, III & IV clinical trial sites, across different therapeutic areas
Assist other team members with co-monitoring activities both remote and on-site
Utilize customer service mindset with sites focusing on delivering value, building loyalty and trust
Act as the main sponsor representative, providing key project updates
Collaborate with the team, developing commitment to study timelines and objectives through regular visits with site staff in-person and remotely
Act as the first point of contact for study sites, escalating any concerns/issues to other departments
Oversee the sites' adherence to GCP/ICH practices, ensuring quality of study conduct

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

Fulltime

New

General Labourer

We are seeking an experienced General Labourer to join our team. This is a vital...

Location

Canada , Richmond Hill

Salary:

18.00 - 20.00 CAD / Hour

Randstad

Expiration Date

April 14, 2026

Requirements

Ability to work in a fast-paced environment
Able to lift up to 50lbs and physically stand and walk for long hours
Completion of high school or equivalent

Job Responsibility

Maintain a clean and organized work area to support a safe and efficient environment for the team
Perform regular inventory counts and replenish stock levels to ensure a steady workflow
Follow all established health and safety protocols, including the consistent use of required personal protective equipment
Complete general operational tasks as assigned to help the team meet daily production targets
Work with colleagues to identify and resolve any discrepancies in orders or stock levels
Lift and move products up to 50 lbs

What we offer

Weekly pay
Opportunity for Temp to Perm

Fulltime

CRA II / Senior CRA

iconplc

Location:
Australia , Sydney or Newcastle

Category:
IT - Administration

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
February 16, 2026

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