CrawlJobs Logo
iconplc Logo iconplc · IT - Administration

Sr CRA

Canada, Montreal · Job Posted May 29, 2026
Apply Position
Job Link Share

Job Description

As a CRA at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programs. This is a sponsor dedicated program focused on monitoring Oncology studies in Montreal.

Job Responsibility

  • Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
  • Running sponsor generated queries efficiently and taking responsibility for study cost efficiency
  • you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required
  • Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff
  • Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements

Requirements

  • University degree in medicine, science, or equivalent
  • Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
  • Excellent written and verbal communication in English
  • Experience monitoring Oncology studies
  • Good social skills enabling you to deal with queries in a timely manner
  • Willingness to travel as required (approximately 60%)

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

Sr CRA

8 matching positions

Senior Clinical Research Associate - FSP

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
South Korea
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology)
  • Fluent in English and in the native language(s) of the country they will work in
  • Extensive knowledge of clinical trial methodologies, ICH/GCP and local country regulations
  • Global clinical trial experience
  • Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent
  • Demonstrated knowledge of clinical research and development processes
  • Demonstrated knowledge of global and local regulatory requirements
  • Demonstrated understanding of key operational elements of clinical research
  • Demonstrated knowledge in disease and technical areas pertaining to clinical studies
  • Demonstrated ability to support sponsor regulatory interactions/inspections
Job Responsibility
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
  • Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock
  • Serve as the primary point of contact for assigned investigator sites
  • Interface with the study team as needed
  • Partner with SCP to perform investigator site development, coaching and training of site personnel
  • Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities
  • Monitor site level adverse events (AEs) and serious adverse events (SAEs)
  • Submit all required reports, documentation, updates and tracking within required timeframes
  • Identify and resolve investigator site issues within required timeframes
What we offer
What we offer
  • Patient-focused culture
  • Supportive and inclusive environment
  • Career growth and development
  • Flexible work arrangements
  • Diverse therapeutic areas and project exposure
  • Advanced Technology
  • Fulltime
Read More
Arrow Right

Senior Clinical Research Associate

Senior Clinical Research Associate - Oncology - East Coast. ICON plc is a world-...
Location
Location
United States , Atlanta; Texas; Maryland; Missouri; Tennessee; North Carolina; Illinois; Ohio; Florida; Philadelphia, PA
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • An undergraduate degree or it’s equivalent in clinical, science, or health related field from an accredited institution
  • a licensed health care professional (i.e. registered nurse) or equivalent work experience required
  • 5+ years clinical monitoring experience required (Sr CRA)
  • Knowledge of ICH and local regulatory authority regulations regarding drug
  • Read, write and speak fluent English
  • Oncology monitoring experience required
  • Experience doing feasibility/site selection/site start up required
  • To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status
Job Responsibility
Job Responsibility
  • Implements and monitors clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and Internation Conference on Harmonization (ICH) Good Clinical Practice (GCP) guidelines
  • Assesses the qualification of potential investigative sites, initiates clinical trials at investigative sites, instructs site personnel on the proper conduct of clinical trials, and closes clinical trials at investigative sites
  • Responsible for site startup activities for assigned sites, including but not limited to regulatory documents collection, informed consent review, IRB/IEC submission support, and budgets and contracts negotiations
  • Reviews and verifies accuracy of clinical trial data collected, either onsite or remotely
  • Provides regular site status information to team members, trial management, and updates trial management tools
  • Completes monitoring activity documents as required by sponsor's SOPs
  • Works closely with other clinical team members to facilitate timely resolution of trial and/or clinical issues
  • Escalates site and trial related issues per Sponsor's SOPs until identified issues are resolved or closed
  • Performs essential document site file reconciliation
  • Performs source document verification and query resolution
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 II - FSP

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
Turkey
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
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
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
What we offer
  • Flexible work arrangements
  • Career growth and development
  • Supportive and inclusive environment
  • Diverse therapeutic areas and project exposure
  • Advanced Technology
Read More
Arrow Right

Qa/qc Coordinator

Airswift is seeking for a QA/QC Coordinator to work in Qatar with a major Oil & ...
Location
Location
Qatar , Doha
Salary
Salary:
Not provided
airswift.com Logo
Airswift Sweden
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BSc, degree, or higher educational qualification in Mechanical or Metallurgical Engineering from recognized Engineering faculty
  • A valid CSWIP 3.2.1 or AWS Sr. welding Inspection Certificate (SCWI) and at least five - year post-certification experiences
  • B Gas Grade 2, or NACE level II Coating inspector qualified is preferable
  • NDT level II in RT, UT, PT & MT/ NDT qualifications against ASNT or ISO requirements
  • Certified QMS Lead Auditor in accordance with ISO 9001:2015 and having at least five - experience in auditing
  • A good knowledge of international codes/standards EN, ISO, API, ASME and ASTM
  • Good leadership skills and good communication skills
  • Ability to work on projects in a complex and multicultural environment
  • Be skilled in using computer programs, MS Office, database management, spreadsheets, and e-mail communications
  • A minimum of fifteen (15) years experiences as QA/QC coordinator / QA/QC Lead, leading QC multidiscipline inspectors’ team, for inspection & testing activities for a major oil and gas projects/ offshore process platforms / jackets/subsea pipeline, including all phases of manufacturing, fabrication, construction, and offshore installation / laying
Job Responsibility
Job Responsibility
  • To lead and coordinate all project quality assurance and quality control activities, ensuring that fabrication, construction, and offshore installation works are executed in full compliance with project specifications, international standards, and approved QA/QC procedures
  • The role acts as the focal point for quality management, supervising inspection teams, monitoring contractor performance, resolving quality issues, and maintaining the integrity of materials, welding, coating, and installation processes across all project phases
  • Fulltime
Read More
Arrow Right
New

Account Executive

At Currys we’re united by one passion: to help everyone enjoy amazing technology...
Location
Location
United Kingdom , West Thurrock
Salary
Salary:
13.86 GBP / Hour
currys.ie Logo
Currys
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Experience working with customers either in a retail or B2B environment (or both!)
  • The drive to achieve targets and exceed customer expectations
  • An eagerness to learn about the latest technology
  • To be confident working in a team.
Job Responsibility
Job Responsibility
  • Making every customer interaction memorable
  • Asking the right questions to match business customers with products
  • Building and maintaining a network of local business owners
  • Growing new business relationships and developing accounts
  • Contributing towards the overall sales performance of the store
  • Being aware of local competitor activities and suggesting ways to stay ahead.
What we offer
What we offer
  • 30 days of annual leave (including bank holiday entitlement)
  • Competitive pension scheme
  • Monthly performance-related bonus
  • Product discounts on the latest tech
  • A range of wellbeing initiatives.
  • Parttime
Read More
Arrow Right
New

Mobile Associate, Store-In-Store - Retail Sales

As a Mobile Associate – Store-in-Store (SiS), you’ll be the face of T-Mobile ins...
Location
Location
United States , Las Vegas
Salary
Salary:
19.50 USD / Hour
https://www.t-mobile.com Logo
T-Mobile
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • High School Diploma/GED (Required)
  • 6 Months Of Customer Service and/or Sales Experience, Retail Environment (Preferred)
  • Customer Satisfaction: Passionate Customer Advocate With The Desire To Be Yourself When Connecting And Having Fun With Our Customers. Effective At Balancing Customer Experience And Performance Goals (Required)
  • Team Building: Desire To Be A Part Of The Game-Changing T-Mobile Store Team. Willingness To Work Alongside Peers And Store Leaders, Learning And Sharing Best Practices, While Serving Customers And Providing Resolutions To Issues. (Required)
  • Retail Sales: Competitive Drive And Confidence To Succeed In A Fast-Paced Sales Environment. (Required)
  • At least 18 years of age
  • Legally authorized to work in the United States
Job Responsibility
Job Responsibility
  • Proactively engages with a broad range of customers in a highly-traffic retail environment. You will use digital tools, communicate effectively, educate customers, and showcase the value of T-Mobile's warehouse/club member benefits
  • Complete training on the T-Mobile store-in-store experience, new skills, products, and processes, and knowledge of systems and reference resources. You will continuously learn and improve your skills to provide the best possible experience for our customers! Will perform skills practicing, knowledge sharing, and store operations
  • At T-Mobile, we are passionate about providing excellent customer experiences, being friendly, and engaging with customers. We can connect on a personal level, match the pace of the customer, establish rapport, trust, and loyalty with every interaction. As a member of our team, you are committed to providing exceptional service, and to exceeding customer expectations. You will proactively attract potential customers to further drive sales activity in your location. You can follow up with customers, collect referrals, handle Be Back processes, and form relationships with new and existing customers.
What we offer
What we offer
  • medical insurance
  • dental insurance
  • vision insurance
  • flexible spending account
  • 401(k)
  • employee stock grants
  • employee stock purchase plan
  • paid time off
  • up to 12 paid holidays
  • paid parental and family leave
  • Parttime
Read More
Arrow Right
New

F&B Trainee - Renaissance Barcelona

Build upon your classroom studies through our Hotel Internship Program opportuni...
Location
Location
Spain , Barcelona
Salary
Salary:
Not provided
https://www.marriott.com Logo
Marriott Bonvoy
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • You must be a current college or university student.
  • Fulltime
Read More
Arrow Right
New

Field Sales Executive

As a Field Sales Executive, you will be the face of myPOS within Venice, working...
Location
Location
Italy , Ancona
Salary
Salary:
Not provided
mypos.com Logo
myPOS
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 2-5+ years of experience in B2B or field sales, with a successful track record
  • Confidence approaching new businesses and starting conversations with decision makers in person
  • A consultative mindset and genuine curiosity about understanding each client's needs before offering solutions
  • The ability to build trust quickly and create long-term relationships
  • The independence and organization to manage your own schedule, territory, and priorities effectively
  • A valid driver's license and willingness to travel regularly within your region
  • Fluency in Italian and English
Job Responsibility
Job Responsibility
  • Proactively identify and approach new business opportunities within the territory of Venice
  • Meet merchants face-to-face to understand their needs and present tailored myPOS solutions
  • Deliver clear, practical product demonstrations and guide clients through the benefits step by step
  • Manage the full sales cycle, from first contact to negotiation and closing
  • Build and maintain strong, long-term relationships with your clients to ensure satisfaction and growth
  • Plan your schedule and territory independently to prioritize high-potential opportunities
  • Represent myPOS professionally at local events, trade fairs, and within the wider business community
What we offer
What we offer
  • Excellent compensation package (base salary + uncapped commission)
  • 25 days annual paid leave
  • Health Insurance
  • Meal Vouchers
  • Travel cost reimbursement
  • Annual salary reviews, promotions and performance bonuses
  • myPOS Academy for upskilling and training
  • Unlimited access to courses on LinkedIn Learning
  • Annual individual training and development budget
  • Refer a friend bonus
  • Fulltime
Read More
Arrow Right