CrawlJobs Logo

Global Clinical Trial Associate

iconplc.com Logo

iconplc

Location Icon

Location:
China , Shanghai

Category Icon
Category:
IT - Administration

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

Not provided
Save Job
Save Icon
Apply Position

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. We are currently seeking a Clinical Associate to join our diverse and dynamic team. As a Clinical Associate at ICON, you will play a pivotal role in supporting the design, implementation, and management of clinical trials, contributing to the advancement of innovative treatments and therapies.

Job Responsibility:

  • Assist in the planning, execution, and monitoring of clinical trials, ensuring adherence to protocol requirements, regulatory guidelines, and industry standards
  • Coordinate study activities including site initiation, patient recruitment, data collection, and monitoring visits to ensure timely and accurate data collection and documentation
  • Collaborate with cross-functional teams including Clinical Operations, Data Management, and Biometrics to support the successful execution of clinical trials
  • Maintain comprehensive study documentation and records, ensuring compliance with applicable regulations and standard operating procedures
  • Support study close-out activities including data cleaning, analysis, and preparation of clinical study reports

Requirements:

  • Bachelor's or advanced degree in Life Sciences, Health Sciences, or a related field
  • Previous experience in clinical research or healthcare, preferably within the pharmaceutical, biotechnology, or CRO industry
  • Strong organizational and time management skills, with the ability to prioritize tasks and manage competing priorities effectively
  • Excellent attention to detail and problem-solving abilities, with a commitment to ensuring data accuracy, integrity, and compliance
  • Effective communication and interpersonal skills, with the ability to collaborate cross-functionally and build strong relationships with study teams and clinical sites
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

Additional Information:

Job Posted:
January 26, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Icon
iconplc - All Job Offers
Job Link Share:
Copy Link Icon
Facebook Icon Twitter Icon LinkedIn Icon

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Global Clinical Trial Associate

Associate Vice President, Clinical Data Management

The Associate Vice President, Clinical Data Management is a member of the Global...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s or master’s degree with 25+ years of data management experience
  • 10 to 15 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources
  • Experience within clinical data management, regulatory compliance, and strategic leadership within a pharmaceutical, biotech, or CRO environment
  • Expertise in GCP, ICH, FDA, EMA regulations, data governance, and clinical trial data standards (CDISC, SDTM)
  • Experience within cross-functional collaborations, leadership, and strategic planning skills, ensuring operational excellence and compliance while driving innovation in data management to support Amgen’s global clinical development efforts
  • Expertise in AI/ML-driven data management solutions, automation, and advanced analytics
  • Understanding of clinical data standards (CDISC, SDTM, ADaM)
  • Experience leading regulatory submissions, including NDA/BLA/MAA filings and advisory committee interactions
  • Proven ability to drive organizational change, optimize processes, and implement lean principles in clinical data management
  • Cross-functional collaboration experience with clinical operations, regulatory affairs, biostatistics, and R&D teams
Job Responsibility
Job Responsibility
  • Develop and drive the global data management strategy in alignment with clinical development objectives and corporate goals
  • Provide strategic and operational leadership to the Clinical Data Management (CDM) function across all clinical programs and phases
  • Lead innovation initiatives, including the implementation of development integration programs and the adoption of cutting-edge technologies to enhance data workflows
  • Represent Clinical Data Management in executive leadership discussions, regulatory interactions, and industry forums
  • Establish and enforce robust clinical data governance models, policies, and risk mitigation strategies to ensure quality and compliance
  • Make final decisions regarding standard operating procedures (SOPs), CDM best practices, and process optimization
  • Engage key stakeholders and ensure timely resolution on critical data integrity and regulatory compliance issues
  • Serve as the primary CDM representative during regulatory inspections and audits, with responsibility for final decisions on findings, responses, and corrective actions
  • Influence cross-functional clinical development, operational, and regulatory strategies through data-driven insights and analytics
  • Partner closely with Clinical Program Operations, Regulatory, Biostatistics, and R&D to ensure seamless integration and alignment of clinical data
Read More
Arrow Right

Senior Associate Data Management

The Senior Associate, Data Management, will help drive key business operation in...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Familiarity with Global Clinical Trial Applications, Marketing Authorizations, Regulations, and Regulatory Guidance
  • In depth understanding of the Veeva Vault system
  • Good written and verbal communication skills
  • Detail oriented
  • Independent time management and prioritization skills
  • Work efficiently with little support and minimal to no supervision
  • Ability to work well with others in demanding situations with a positive attitude demonstrating tact, diplomacy, and respect
  • Critical thinking skills
  • Appropriate software skills as required
  • Strong analytical and problem solving, communication and presentation skills
Job Responsibility
Job Responsibility
  • Responsible for maintaining data within the Regulatory Information Management (RIM) system
  • Create and archive clinical trial, marketing application submissions and health Authority correspondence within Amgen’s RIM system
  • Serve as a Data Management SME within cross-functional collaborative initiatives
  • Deliver the implementation of new processes within Veeva Vault, XeVMPD, IDMP and other key regulatory initiatives, ensuring alignment with global regulatory standards and business objectives
  • Provide support on creating, running and analysing reports for data streamline projects
  • Develop and deliver training materials and presentations to a global audience
  • Manage the protocol Amendment New Investigator (PANI) submission updates
  • Manage 1572 forms for FDA submission
  • Provide support within the global data management team on US Certificate of Pharmaceutical Product (CPP) and EU Certificate of Medicinal Product (CMP) during additional workload periods
  • Adhere to Amgen processes, policies, guidelines, SOPs and training documentations
What we offer
What we offer
  • Competitive and comprehensive Total Rewards Plans aligned with local industry standards
Read More
Arrow Right

Clinical Trial Manager

Clinical Trial Manager - Early Oncology
Location
Location
United States , CARY, BLUE BELL, BASKING RIDGE, NJ, CHICAGO, IL
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BA/BS degree with at least 3 years clinical trial experience or advanced degree (MS/PhD/PharmD) with at least 2 years clinical trial experience
  • Must have strong knowledge of ICH/GCP guidelines and regulatory requirements
  • Must have knowledge of protocol and clinical drug development processes, clinical trial design, trial planning and management, and monitoring
  • Requires project management skills and trial leadership ability
  • Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer ability
  • Fluent in English
  • Experience in Phase I oncology
  • Global experience with primary focus on independent vendor set up and management, oncology cohort management and experience in supporting dose escalation safety meetings.
Job Responsibility
Job Responsibility
  • Manage the day-to-day operations of assigned trials and responsibilities to ensure completion per established project team goals and objectives in compliance with applicable GCP/ICH guidelines and other regulatory requirements
  • Leads or supports cross-functional trial teams, including vendors
  • Ensures accurate and up-to-date trial information within relevant tracking systems and provide regular updates of trial progression to Clinical Operations Lead, Clinical Trial Lead, and other defined stakeholders
  • Proactively identify and resolve issues that arise during trial conduct
  • manage escalation of trial-related issues
  • Participate in or lead the development of core trial documents, trial plans and system set-up
  • participate in preparation and ensure operational excellence of protocol and implementation of appropriate systems, standards, and processes to ensure quality across investigative sites, vendors, and data
  • Participate in or lead preparation of vendor requirements and project scope and selection of trial vendors
  • effectively manage interactions and escalations with vendor trial team
  • Participate in or lead feasibility assessment and selection of countries and sites for trial conduct
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

Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects
  • At least 4 years of statistical programming experience in a clinical development environment
  • Familiarity with drug development life cycle
  • Excellent skills with the manipulation, analysis and reporting of complex clinical trial data
  • Ability to effectively perform complex statistical programming and related tasks
  • Ability to provide quality output and deliverables in adherence with challenging timelines
  • Ability to work effectively on multiple tasks or projects across therapeutic areas
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
  • Working knowledge of latest CDISC SDTM standards
  • Familiar with CDISC ADaM and Define standards with strong ability to implement the standards
Job Responsibility
Job Responsibility
  • Perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions
  • Analysis and reporting of clinical trial data using SAS and/or R
  • Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
  • Creation and validation of complex tables, listings, and figures, both safety and efficacy
  • Prepare statistical programming specifications
  • Prepare statistical programming related documents for regulatory submissions
  • Maintain tracking and validation documentation
  • Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
  • Interact and collaborate with study team members from other functions globally
  • Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP
What we offer
What we offer
  • Vast opportunities to learn and move up and across our global organization
  • Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
  • Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
Read More
Arrow Right

Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects
  • At least 4 years of statistical programming experience in a clinical development environment
  • Familiarity with drug development life cycle
  • Excellent skills with the manipulation, analysis and reporting of complex clinical trial data
  • Ability to effectively perform complex statistical programming and related tasks
  • Ability to provide quality output and deliverables in adherence with challenging timelines
  • Ability to work effectively on multiple tasks or projects across therapeutic areas
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
  • Working knowledge of latest CDISC SDTM standards
  • Familiar with CDISC ADaM and Define standards with strong ability to implement the standards
Job Responsibility
Job Responsibility
  • Perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions
  • Analysis and reporting of clinical trial data using SAS and/or R
  • Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
  • Creation and validation of complex tables, listings, and figures, both safety and efficacy
  • Prepare statistical programming specifications
  • Prepare statistical programming related documents for regulatory submissions
  • Maintain tracking and validation documentation
  • Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
  • Interact and collaborate with study team members from other functions globally
  • Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP
What we offer
What we offer
  • Vast opportunities to learn and move up and across our global organization
  • Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
  • Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
Read More
Arrow Right

Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects
  • At least 4 years of statistical programming experience in a clinical development environment
  • Familiarity with drug development life cycle
  • Excellent skills with the manipulation, analysis and reporting of complex clinical trial data
  • Ability to effectively perform complex statistical programming and related tasks
  • Ability to provide quality output and deliverables in adherence with challenging timelines
  • Ability to work effectively on multiple tasks or projects across therapeutic areas
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
  • Working knowledge of latest CDISC SDTM standards
  • Familiar with CDISC ADaM and Define standards with strong ability to implement the standards
Job Responsibility
Job Responsibility
  • Perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions
  • Analysis and reporting of clinical trial data using SAS and/or R
  • Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
  • Creation and validation of complex tables, listings, and figures, both safety and efficacy
  • Prepare statistical programming specifications
  • Prepare statistical programming related documents for regulatory submissions
  • Maintain tracking and validation documentation
  • Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
  • Interact and collaborate with study team members from other functions globally
  • Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP
What we offer
What we offer
  • Vast opportunities to learn and move up and across our global organization
  • Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
  • Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
  • Fulltime
Read More
Arrow Right

Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects
  • At least 4 years of statistical programming experience in a clinical development environment
  • Familiarity with drug development life cycle
  • Excellent skills with the manipulation, analysis and reporting of complex clinical trial data
  • Ability to effectively perform complex statistical programming and related tasks
  • Ability to provide quality output and deliverables in adherence with challenging timelines
  • Ability to work effectively on multiple tasks or projects across therapeutic areas
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
  • Working knowledge of latest CDISC SDTM standards
  • Familiar with CDISC ADaM and Define standards with strong ability to implement the standards
Job Responsibility
Job Responsibility
  • Perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions
  • Analysis and reporting of clinical trial data using SAS and/or R
  • Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
  • Creation and validation of complex tables, listings, and figures, both safety and efficacy
  • Prepare statistical programming specifications
  • Prepare statistical programming related documents for regulatory submissions
  • Maintain tracking and validation documentation
  • Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
  • Interact and collaborate with study team members from other functions globally
  • Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP
What we offer
What we offer
  • Vast opportunities to learn and move up and across our global organization
  • Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
  • Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
Read More
Arrow Right

Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects
  • At least 4 years of statistical programming experience in a clinical development environment
  • Familiarity with drug development life cycle
  • Excellent skills with the manipulation, analysis and reporting of complex clinical trial data
  • Ability to effectively perform complex statistical programming and related tasks
  • Ability to provide quality output and deliverables in adherence with challenging timelines
  • Ability to work effectively on multiple tasks or projects across therapeutic areas
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
  • Working knowledge of latest CDISC SDTM standards
  • Familiar with CDISC ADaM and Define standards with strong ability to implement the standards
Job Responsibility
Job Responsibility
  • Perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions
  • Analysis and reporting of clinical trial data using SAS and/or R
  • Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
  • Creation and validation of complex tables, listings, and figures, both safety and efficacy
  • Prepare statistical programming specifications
  • Prepare statistical programming related documents for regulatory submissions
  • Maintain tracking and validation documentation
  • Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
  • Interact and collaborate with study team members from other functions globally
  • Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP
What we offer
What we offer
  • Vast opportunities to learn and move up and across our global organization
  • Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
  • Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
Read More
Arrow Right
Jobs by Category
Art and Entertainment Jobs Banking Jobs Call Center Jobs Construction Jobs Consulting Jobs Customer Service Jobs Education Jobs Energy Jobs Finance Jobs Gastronomy Jobs Health and Beauty Jobs Hospitality and Tourism Jobs Human Resources Jobs Insurance Jobs IT - Administration Jobs IT - Software Development Jobs Legal Jobs Logistics Jobs Manufacturing Jobs Marketing, Digital Marketing, SEO, SEM Jobs Media Jobs Nursing Jobs Office Administration Jobs Pharmacy Jobs Physical Work Jobs Public Relations Jobs Public Sector Jobs Purchasing Jobs Quality Control Jobs Real Estate Jobs Research and Development Jobs Sales Jobs
Job Positions Jobs by Country
United States Jobs United Kingdom Jobs India Jobs Canada Jobs Australia Jobs Germany Jobs Ireland Jobs Poland Jobs
Company
Blog About Us Contact
Follow Us
Facebook
X (Twitter)
LinkedIn
Instagram
CrawlJobs Group
ITFlashcards AllDevBlogs
© 2026 CrawlJobs Ltd. All Rights Reserved
Terms & Conditions Privacy Policy