IQVIA · 3 days ago
Clinical Trial Learning and Development Analyst
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. The Clinical Trial Learning and Development Analyst will provide support for study-specific training planning, ensuring compliance with SOPs and GCP while developing effective training materials and collaborating with study teams.
AnalyticsHealth CareLife Science
Responsibilities
Services rendered will adhere to applicable Johnson & Johnson SOPs, WIs, policies, codes of Good Clinical Practice (GCP), local regulatory requirements, etc
Develop and document the study-specific training plan for assigned studies
Conduct and/or supports needs assessments to determine the full scope of study level training needs while considering potential challenge areas to focus on based on available data and in-depth discussions with the Global Study Team
Support end-to-end development of study specific training strategy from concept to the design, development, and maintenance of effective training materials in accordance with Standard Operating Procedures and Good Clinical Practice while also considering adult learning principles
Manages content of training repository with appropriate mechanisms in place to support version control and compliance
Manage project timelines between Study Teams and/or Vendors
May develop training modules using approved authoring tools (e.g., SCORM, MP4, etc.)
Contribute to lessons learned and overall continuous improvement
Collaborate with subject matter experts to facilitate the creation of training materials
Supports oversight of operations process, tools and reporting and ensures necessary training/ support established
Proactively identify issues to study team contacts and collaboratively develop solutions
Responsible for championing the study-specific training process across the organization
Contributes to onboarding new CTL&D colleagues, including mentoring others on study-specific training process and requirements
May contribute as a representative of functional area in process initiatives, as required
Complies with relevant training requirements
Qualification
Required
Bachelor's degree required
2+ years of clinical trial operation experience
Strong working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures
Strong IT skills in appropriate software and company systems
Willingness to travel with occasional overnight stay
Proficient in speaking and writing in English
Preferred
Degree in a health or science related field preferred
Experience within developing study specific training plans highly preferred
Benefits
Incentive plans
Bonuses
Health and welfare and/or other benefits
Company
IQVIA
IQVIA provides analytics, compliance, and management solutions to the life sciences industry.
H1B Sponsorship
IQVIA has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (167)
2024 (294)
2023 (261)
2022 (229)
2021 (208)
2020 (180)
Funding
Current Stage
Public CompanyTotal Funding
$3.5B2025-06-02Post Ipo Debt· $2B
2023-11-14Post Ipo Debt· $500M
2023-05-18Post Ipo Debt· $1B
Leadership Team
Recent News
Sabin Vaccine Institute
2025-12-04
Company data provided by crunchbase