**Job Summary:** CTL&T Analyst provides support to CTL&T for study-specific training planning within various therapeutic area(s). Service/deliverables include support to deliver on study-specific training related processes, including, but not limited to development/ documentation of the study-specific training plan for each protocol assigned. Further, services may include project related work, as assigned by CTL&T Leads and/or Leadership, and will ensure quality and that work is compliant with company Standard Operating Procedures (SOPs). Partners with CTL&T colleagues, Learning Systems Solutions (LSS) organization, and designated study team trial leaders to ensure training plan is documented and implemented in appropriate systems with supporting documentation. **Deliverables:** + Services rendered will adhere to applicable Johnson & Johnson SOPs, WIs, policies, codes of Good Clinical Practice (GCP), local regulatory requirements, etc. + Complies with relevant training requirements. + 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&T colleagues, including mentoring others on study-specific training process and requirements. + May contribute as a representative of functional area in process initiatives, as required. **Education and Experience Requirements:** + Bachelor’s degree required + Degree in a health or science related field preferred + 2+ years of clinical trial operation experience. + Experience within developing study specific training plans highly preferred. + 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. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role, when annualized, is $68,400.00 - $171,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled