Student Veterans of America Jobs

Welcome to SVA’s jobs portal, your one-stop shop for finding the most up to date source of employment opportunities. We have partnered with the National Labor Exchange to provide you this information. You may be looking for part-time employment to supplement your income while you are in school. You might be looking for an internship to add experience to your resume. And you may be completing your training ready to start a new career. This site has all of those types of jobs.

Here are a few things you should know:
  • This site is mobile friendly. You do not need a log-in or password to access information.
  • Jobs on this site are original and unduplicated and come from three sources: the Federal government, state workforce agency job banks, and corporate career websites. All jobs are vetted to ensure there are no scams, training schemes, or phishing.
  • The site is refreshed daily to remove out-of-date content.
  • The newest jobs are listed first, so use the search features to match your interests. You can look for jobs in a specific geographical location, by title or keyword, or you can use the military crosswalk. You may want to do something different from your military career, but you undoubtedly have skills from that occupation that match to a civilian job.

Job Information

IQVIA Associate Manager, Clinical Trials Regulatory Management (m/w/d) - Home-based, Europe in Livingston, United Kingdom

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects.

RESPONSIBILITIES

  • Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex

  • Ability to administratively and technically/scientifically review core scientific documentation and feedback gap analysis to customers.

  • Prepares and maintains core clinical trial submission dossiers in accordance with applicable regulatory requirements.

  • Ability to write scientific documents e.g. Investigational Medicinal Product Dossier, clinical trial justifications with minimum support of senior staff

  • May strategically plan and perform European centralized submissions and facilitate global submissions

  • May provide support on regulatory business development opportunities and complete Data Informed Protocol Assessments (DIPAs)

  • Understands the Scope of Work, deliverables and budget for any given project and ensure timelines are met.

  • Ensures accurate completion, maintenance and adherence to internal systems, databases, tracking tools and project plans in line with agreed SOPs (customer and/or IQVIA).

  • Deliver regulatory training/presentations as required.

  • May perform additional tasks as deemed appropriate by Line Manager

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

  • Good understanding of the regulations, directives and guidance supporting clinical Research and Development

  • Demonstrates comprehensive regulatory/technical expertise

  • Good negotiating skills and the ability to identify and resolve issues, using flexible adaptable approach

  • Strong ownership and oversight skills

  • Demonstrated skills in chairing small meetings

  • Ability to work on several projects, retaining quality and timelines and can prioritize workload with minimal supervision

  • Ability to establish and maintain effective working relationships with co-workers, managers and clients

  • Strong software and computer skills, including MS Office applications

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

  • Degree in life science-related discipline or professional equivalent plus at least 5 years relevant experience* or high school diploma plus at least 9+ years’ experience* (*or combination of education, training and experience)

PHYSICAL REQUIREMENTS

  • Extensive use of telephone and face-to-face communication requiring accurate perception of speech

  • Extensive use of keyboard requiring repetitive motion of fingers

  • Regular sitting for extended periods of time

  • Travel might be required

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.

To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.

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