CrawlJobs Logo
iconplc Logo iconplc · Research and Development

Senior Clinical Research Associate

Belgium, Mechelen · Job Posted January 16, 2026
Apply Position
Job Link Share

Job Description

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. For our client in the Antwerp region, we are looking for a Senior Clinical Research Associate (CRA) (Senior Site Manager) to join our ICON team! You will be working for one of the most attractive employers in Belgium, creating a real impact on the health of patients worldwide. The Senior Site Manager operates independently with minimal supervision and may support process improvement, training, and mentoring of other Site Managers.

Requirements

  • Serve as the primary local company contact for assigned trial sites
  • Participate in site feasibility, qualification visits, and investigator meetings
  • may support preparation and presentations
  • Independently manage all site activities across start-up, initiation, monitoring (including remote), maintenance, and close-out in compliance with SOPs and policies
  • Implement risk-based monitoring and ensure timely resolution of site issues
  • Ensure site staff training is completed and documented
  • support rapid site activation in collaboration with the study team
  • Support site recruitment strategies and contingency planning
  • Oversee site supplies, including clinical and non-clinical materials, drug accountability, storage, returns, and destruction
  • Ensure timely, accurate data entry, query resolution, and data integrity
  • Ensure timely reporting and documentation of AEs, SAEs, and PQCs
  • Maintain complete, accurate trial documentation and systems records
  • prepare monitoring reports and follow-up letters
  • Collaborate with the LTM and central team to communicate site progress, risks, and issues
  • Support QA audits, CAPA development, and inspection readiness
  • Prepare and conduct site close-out visits
  • ensure archiving and retention requirements are met
  • Track site-level costs and ensure payments, where applicable
  • Build and maintain strong relationships with investigators, site staff, and internal stakeholders
  • Act as a protocol and site management subject matter expert
  • comply with training requirements
  • May support HA and IEC/IRB submissions as needed
  • Coach and mentor junior Site Managers when required.

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.
iconplc - All Job Offers

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Suggested Tags: Frontend Developer Secretary Talent Manager Salesforce Administrator Data Analyst
Similar Jobs for

Senior Clinical Research Associate

8 matching positions

Senior Clinical Research Associate

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
Israel
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Extensive experience in site management, with knowledge of clinical trial methodology and terminology
  • Experience in oncology trials, at least 5 years
  • Minimum 5 years’ experience in independent supervision of all types of visits
  • Effective time management, organizational and interpersonal skills and problem-solving skills, with the ability to multi-task and priorities
  • Good understanding and working knowledge of clinical research, clinical trial phases, current GCP/ICH and country clinical research legislation and guidelines
Job Responsibility
Job Responsibility
  • You will be dedicated to a single client
  • You will be responsible for all site management and supervisory activities in the assigned oncology studies
  • You will work with industry leaders and subject matter experts
  • You will have the opportunity to mentor junior CRAs
  • You will work with world-class technology
  • You will have great opportunities to travel, work from home, meet new people and play a key role in the drug development process
What we offer
What we offer
  • Premium salary
  • Attractive benefits
  • Car or company car
  • Medical care plan: Health, Dental & Vision
  • Life Assurance
  • Excellent work environment
  • Culture of teamwork and collaboration
  • People who motivate and face challenges together
  • Innovative technology
  • Excellent training
Read More
Arrow Right
New

Senior Clinical Research Associate

Location
Location
Canada , Montreal, Ontario, Toronto
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • 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
  • Willingness to travel as required (approximately 60%)
  • Bilingual in French and English
Job Responsibility
Job Responsibility
  • Lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement
  • 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
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
Read More
Arrow Right
New

Senior Clinical Research Associate

We are currently seeking a Sr Clinical Research Associate to join our diverse an...
Location
Location
United States , Multiple US locations
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in a scientific or healthcare-related field
  • Minimum of 5 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
  • Experience in ophthalmology or gene therapy studies
  • 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
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
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
Read More
Arrow Right

Senior Clinical Research Associate

Senior CRA-Oncology-Home Based-South Korea-ICON Strategic Solutions. ICON plc is...
Location
Location
South Korea , Seoul
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • 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
  • Willingness to travel as required (approximately 60%)
Job Responsibility
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
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
Read More
Arrow Right

Senior Clinical Research Associate

ICON plc is a world-leading healthcare intelligence and clinical research organi...
Location
Location
France , Paris
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • 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
  • Willingness to travel as required (approximately 60%)
Job Responsibility
Job Responsibility
  • Lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement
  • 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
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
Read More
Arrow Right

Senior Clinical Research Associate

Senior Clinical Research Associate - Cardio (Smart Pulse A-fib) - All Regions. I...
Location
Location
United States , Kansas City; Chicago; Los Angeles; Pennsylvania; Georgia; Texas
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 3 years of monitoring experience required
  • A bachelor's degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science
  • In-depth knowledge of FDA regulations and ICH/GCP guidelines
  • Strong problem-solving skills to mitigate risks and identify issues at sites and implement effective solutions promptly
  • Strong interpersonal skills to establish and maintain effective working relationships with site personnel, investigators, and internal teams
  • Exceptional verbal and written communication skills, with the ability to convey complex information clearly and concisely
  • Ability to tailor communication style to the needs and preferences of different stakeholders, fostering a collaborative environment
  • Ability to work independently and manage multiple priorities in a dynamic environment
  • A well-executed plan for communication with the study teams and sites
  • Well-versed in clinical trial management
Job Responsibility
Job Responsibility
  • support 1 study in the cardiovascular/electrophysiology medical device space
What we offer
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
Read More
Arrow Right

Senior Clinical Research Associate

Senior Clinical Research Associate - Neurovascular - Midwest/Central ICON plc i...
Location
Location
United States , TEXAS, MISSOURI, BLUE BELL, WISCONSIN, CHICAGO
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • A bachelor's degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science
  • 3 years of monitoring required (medical device, pharma, CRO industry)
  • The ideal candidate will have medical device monitoring experience- however, pharma monitoring experience will be considered
  • Neuro or Neurovascular monitoring experience a plus
  • Located in Central/Midwest region (willing to travel to west coast and east coast as needed)
  • In-depth knowledge of FDA regulations and ICH/GCP guidelines
  • Strong problem-solving skills to mitigate risks and identify issues at sites and implement effective solutions promptly
  • Strong interpersonal skills to establish and maintain effective working relationships with site personnel, investigators, and internal teams
  • Exceptional verbal and written communication skills, with the ability to convey complex information clearly and concisely
  • Ability to tailor communication style to the needs and preferences of different stakeholders, fostering a collaborative environment
Job Responsibility
Job Responsibility
  • independently monitors trials either onsite or remotely, ensuring compliance with protocols, ICH-GCP guidelines, ICON and/or customer SOPs, and applicable regulatory requirements
  • supports complex studies, contributes to operational excellence, and serves as a mentor to junior staff, while maintaining site readiness for audits and inspections
What we offer
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
Read More
Arrow Right

Senior Clinical Research Associate

We are currently seeking a Senior Clinical Research Associate (CRA) to join our ...
Location
Location
South Korea , Seoul
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
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
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
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
Read More
Arrow Right