1

Veeva Clinical Jobs in Indiana (NOW HIRING)

Lead Internal Auditor, GLP/GCP

Indianapolis, IN

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... clinical research laboratory testing operations comply with global regulatory standards and ... Experience with compliance software such as Veeva or Trackwise. At Labcorp, you can expect the ...

Lead Internal Auditor, GLP/GCP

Indianapolis, IN · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... clinical research laboratory testing operations comply with global regulatory standards and ... Experience with compliance software such as Veeva or Trackwise. At Labcorp, you can expect the ...

About eGenesis eGenesis is a clinical-stage biotechnology company developing human-compatible ... Create and revise safety-related SOPs for integration into Qualio/Veeva (controlled document ...

Associate, Quality Operations

Indianapolis, IN · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... clinical trials Essential Familiarity of eQMS systems such as Veeva Desired Knowledge of cGxPs, clean room controls, aseptic processing, and EMA and ISO standards for cleanrooms Desired ON-THE-JOB ...

Showing results 21-39

Veeva Clinical information

What is a Veeva Clinical professional?

A Veeva Clinical professional is someone who specializes in using the Veeva Vault Clinical Suite, a cloud-based platform designed to manage clinical trial processes and data in the life sciences industry. Their responsibilities often include implementing, configuring, and supporting Veeva Vault Clinical applications such as eTMF, CTMS, and Study Startup. These professionals help organizations streamline clinical operations, ensure regulatory compliance, and improve collaboration across trial teams. Their expertise is highly valued by pharmaceutical, biotech, and contract research organizations.

What are the key skills and qualifications needed to thrive as a Veeva Clinical specialist?

To thrive as a Veeva Clinical Specialist, you need a solid understanding of clinical trial processes, data management, and life sciences regulations, often supported by a degree in life sciences or related fields. Familiarity with Veeva Vault Clinical Suite, electronic data capture (EDC) systems, and relevant certifications like Veeva Vault Administrator are highly valued. Strong analytical thinking, attention to detail, and effective communication are essential soft skills for collaborating with cross-functional teams and clients. These competencies ensure the optimization of clinical workflows, regulatory compliance, and successful implementation of Veeva solutions in clinical research environments.

What are some common challenges faced by professionals working in Veeva Clinical roles, and how can they be addressed?

Professionals in Veeva Clinical roles often encounter challenges such as adapting to frequent software updates, ensuring data integrity across multiple studies, and coordinating with cross-functional teams like clinical operations and IT. Staying current with new features and best practices is essential to maximize the platform's capabilities. Proactive communication and ongoing training can help address these challenges, as well as building strong relationships with stakeholders to streamline workflows and resolve issues efficiently.

What are popular job titles related to Veeva Clinical jobs in Indiana?

For Veeva Clinical jobs in Indiana, the most frequently searched job titles are:

Lead Internal Auditor, GLP/GCP

Labcorp

Indianapolis, IN

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 24 days ago


Labcorp rating

6.6

Company rating: 6.6 out of 10

Based on 1,145 frontline employees who took The Breakroom Quiz

97th of 120 rated laboratories


Job description


Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world's most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you'll have the opportunity to do meaningful work, grow your career and make a real impact on people's health around the world. Together, we're improving health and improving lives.


Labcorp is seeking a Lead Internal Auditor, GLP/GCP to join our team in Indianapolis, IN!

Work Schedule: Monday Through Friday 8-5 pm

Job Responsibilities:

The Lead Internal Auditor plays a pivotal role as part of our Quality Assurance team in ensuring that clinical research laboratory testing operations comply with global regulatory standards and industry-recognized best practices, including GCP/GLP, ISO 15189, ISO 13485 and CAP.

This position leads the internal audit program execution, drives process improvements, collaborates with management to implement audit strategies, mentors' junior auditors, and collaborates with cross-functional teams to uphold quality and regulatory integrity across clinical laboratory testing and operational environments. The ideal candidate will possess strong leadership skills, a keen eye for detail, and the ability to oversee complex audit functions in a fast-paced environment with minimal direction. This role requires initiative-taking, timely and responsive engagement with stakeholders, ensuring compliance with industry regulations and internal standards while continuously improving auditing processes.

Focus areas include:

  • Managing the Internal Audit Program

  • Preparedness and Oversight

  • Audit Hosting & Regulatory Support

  • Severity Finding and Audit Report Review with Management

  • Audit Program Monitoring

  • Internal Auditor Development

  • Quality Assurance (QA) Support

Minimum Qualifications:

  • Bachelor's degree in a Pharmacy, Chemistry or Biology.

  • 8 or more years of experience in GLP/GCP regulatory environment.

  • 4 or more years of experience in Laboratory or Quality with ISO 15189/ISO 13485 and CAP.

Preferred Qualifications:

  • Master's degree in science or management

  • 8 or more years of experience in regulatory environment with GCP/GLP, ISO 15189, ISO 13485, and CAP

  • 2 or more years of experience as a Lead Internal Auditor

  • ASQ Quality Auditor Certification

  • ASQ Quality Manager Certification

  • ASQ Quality Engineer Certification

Additional Job Standards:

  • Ability to demonstrate effective communication verbally and written with an emphasis on strategic communication with clients.

  • Excellent organizational and project management abilities.

  • Strong negotiation, influencing, and networking skills.

  • Demonstrative skills include risk management application experience including risk-based auditing methodologies.

  • Experience in training and developing internal auditors.

  • Experience with quality management system and regulatory compliance inspections

  • Experience leading process improvement initiatives.

  • Experience with compliance software such as Veeva or Trackwise.

At Labcorp, you can expect the following:

  • Innovative Environment: Join a leading healthcare organization committed to driving innovation through internal development to help improve health and improve lives.

  • Collaborative Culture: Work in a dynamic, inclusive environment that values diverse perspectives and fosters collaboration.

If you have a passion for compliance auditing and a drive for operational excellence, join our growing Quality team as a GLP/GCP Lead Internal Auditor and take your career to the next level at Labcorp. Imagine being involved in innovation and projects that change the course of our industry daily!

Benefits:Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan.For more detailed information, pleaseclick here.


Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.


We encourage all to apply

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit ouraccessibility siteor contact us atLabcorp Accessibility. Formore information about how we collect and store your personal data, please see ourPrivacy Statement.



What Labcorp employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom