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Weekend Clinical Trial Transparency Jobs in Georgia

LivaNova

Statistical Programmer II

Atlanta, GA

$90K - $100K/yr

Relevant experience in clinical trial programming, clinical data analysis, statistical programming ... Pay Transparency * A reasonable estimate of the annual base salary for this position is $90,000 ...

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Weekend Clinical Trial Transparency information

What is a weekend clinical trial transparency role?

A Weekend Clinical Trial Transparency role involves ensuring that clinical trial data and results are accurately and ethically disclosed to the public, often by managing documentation, reporting, and compliance with regulatory requirements over the weekend. Professionals in this role work to maintain transparency in clinical research by preparing trial summaries, updating clinical trial registries, and responding to disclosure queries. This helps uphold ethical standards, increases public trust, and supports regulatory compliance. Weekend positions are often needed to provide continuous support, address urgent requests, and meet tight submission deadlines.

What are the key skills and qualifications needed to thrive as a weekend clinical trial transparency specialist?

To excel as a Weekend Clinical Trial Transparency Specialist, you need a solid understanding of clinical research protocols, regulatory requirements, and strong attention to detail, often supported by a background in life sciences or related fields. Familiarity with clinical trial registries (such as ClinicalTrials.gov), data management systems, and relevant compliance frameworks is essential. Strong organizational skills, effective written communication, and the ability to work independently are standout soft skills in this role. These competencies ensure accurate, timely, and compliant disclosure of clinical trial information, which is critical for regulatory adherence and public trust.

How does working in a weekend clinical trial transparency role differ from weekday positions, and what should applicants expect regarding work-life balance?

Weekend Clinical Trial Transparency roles often require ensuring that clinical trial data is accurately disclosed and compliant with regulatory standards during non-standard business hours. Applicants can expect to work independently or with a small weekend team, communicating remotely with weekday staff as needed. While weekend shifts can offer flexibility and potentially less overlap with meetings, the role may involve resolving urgent disclosure issues or assisting with last-minute updates to trial registries. Maintaining clear documentation and proactive communication with the broader team are key for success and continuity across shifts.

What are the most commonly searched types of Clinical Trial Transparency jobs in Georgia?

The most popular types of Clinical Trial Transparency jobs in Georgia are:

What are popular job titles related to Weekend Clinical Trial Transparency jobs in Georgia?

For Weekend Clinical Trial Transparency jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Weekend Clinical Trial Transparency jobs in Georgia look for?

The top searched job categories for Weekend Clinical Trial Transparency jobs in Georgia are:

What cities in Georgia are hiring for Weekend Clinical Trial Transparency jobs?

Cities in Georgia with the most Weekend Clinical Trial Transparency job openings:

Weekend Clinical Trial Transparency jobs near you

Clinical Trial Material Manager (2nd Shift)

IQVIA

Marietta, GA

$77K - $161K/yr

Full-time

Medical, Life

Re-posted 21 days ago

Key responsibilities

  • Lead, coach, and develop a team of direct reports in a dynamic production environment

  • Manage daily and long-range production schedules to meet customer demand and service-level production targets

  • Coordinate daily with Project Management, Warehouse, Logistics, Quality, and IT to resolve production issues and prevent delays

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 226 rated it services

Job description

We are seeking Clinical Trial Material Manager (2nd Shift) to join IQVIA Laboratories at Marietta, GA.
We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.
Job Summary:
The Clinical Trial Material Manager leads daily second-shift (2:00 PM to 11:00 PM) manufacturing operations in a regulated, high-volume production environment. This role ensures on-time delivery, quality compliance, staff performance, and continuous improvement while partnering across Project Services, Warehouse, Logistics, Quality, and IT.
What You'll Be Doing:
  • Lead, coach, and develop a team of direct reports in a dynamic production environment
  • Manage daily and long-range production schedules to meet customer demand and service-level production targets
  • Prioritize urgent, same-day, and future-dated work orders to ensure on-time delivery
  • Coordinate daily with Project Management, Warehouse, Logistics, Quality, and IT to resolve production issues and prevent delays
  • Utilize LIMS to support production files, platform reports, production metrics, dashboards, and compliance reporting
  • Perform root cause investigations for quality incidents, customer complaints, operations incidents, and in-process deviations
  • Lead and support Lean, Six Sigma, and process improvement initiatives to optimize production flow and reduce bottlenecks
What We Are Looking For:
  • Bachelor's degree, 10 years of experience in lieu of degree
  • Minimum 5 years of people management experience, managing 20 employees in a manufacturing environment
  • Minimum 5 years of experience managing manual assembly or production lines
  • Minimum 2 years of experience leading process improvement projects
  • Working knowledge of Microsoft Excel, Outlook, and PowerPoint
  • Working knowledge of ICH, GMP, and OSHA regulations
  • Six Sigma Yellow or Green Belt experience required; certification preferred
  • Other equivalent combination of education, training, and experience may be accepted in lieu of degree
The Knowledge, Skills and Abilities Needed for This Role:
  • Strong leadership, coaching, and staff development skills in a high-volume production environment
  • Ability to prioritize urgent and business-critical work while maintaining quality and compliance expectations
  • Effective cross-functional communication skills with the ability to escalate risks, constraints, and operational performance updates
  • Strong problem-solving skills with the ability to conduct investigations and drive root cause analysis
  • Ability to support overtime, weekends, and holidays based on critical business needs and accelerated trial timelines
What We Offer You:
We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.
To learn more about our benefits, visit https://jobs.iqvia.com/benefits.
If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!

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 athttps://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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $77,700.00 - $161,800.00. 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.

What IQVIA employees say

Pay

Benefits

Hours and flexibility

Workplace

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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