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Veeva Clinical Jobs (NOW HIRING)

Leading workstreams for Veeva Vault-enabled transformation programs across regulatory, clinical, quality, or safety functions * Managing project plans, deliverables, risks, issues, and stakeholder ...

Life Science Veeva Manager

Cincinnati, OH · On-site

$60K - $66K/yr

Leading workstreams for Veeva Vault-enabled transformation programs across regulatory, clinical, quality, or safety functions * Managing project plans, deliverables, risks, issues, and stakeholder ...

Technical Product Manager - AI Solutions

$170K - $197K/yr

They are looking for an experienced technical product manager to design and deliver high-value AI Agent solutions for Veeva Development Cloud, focusing on improving the efficiency of clinical trials ...

Veeva Vault implementations of Veeva RIM, Clinical, Quality, and/or Safety * Digital transformations / innovations * Understanding of Veeva data models, data structures, standards, and governance ...

Collaborate with QA on central depot document management in Veeva. * Partner with Clinical on IRT selection, implementation, and UAT. * Manage cold-chain logistics for Clinically Labelled Drug ...

New

Senior Product Manager - Patient CRM

$129K - $170K/yr

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences ... Translate the complexities of patient journeys, including reimbursement, clinical trial support ...

Collaborate with QA on central depot document management in Veeva. * Partner with Clinical on IRT selection, implementation, and UAT. * Manage cold-chain logistics for Clinically Labelled Drug ...

... Veeva Vault. Key accountabilities include generating documents such as protocol, investigator ... The Director, Clinical Medical Writing will develop new SOPs and templates and contribute towards ...

Be Seen First

Utilize Veeva Vault for trial master file and document management * Ensure adherence to study ... Extensive experience as a Clinical Research Coordinator in outpatient or clinical trial settings

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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 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 the key skills and qualifications needed to thrive as a Veeva Clinical Specialist, and why are they important?

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.
More about Veeva Clinical jobs
What cities are hiring for Veeva Clinical jobs? Cities with the most Veeva Clinical job openings:
What states have the most Veeva Clinical jobs? States with the most job openings for Veeva Clinical jobs include:
Infographic showing various Veeva Clinical job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.
Life Science Veeva Manager

Life Science Veeva Manager

Deloitte

Nashville, TN

Other

Posted 5 days ago


Deloitte rating

8.1

Company rating: 8.1 out of 10

Based on 90 frontline employees who took The Breakroom Quiz

58th of 150 rated financial services


Job description

Passionate about helping Life Sciences organizations navigate strategic, operational, and regulatory priorities while driving meaningful transformation? If you're excited to work across multidisciplinary teams to deliver innovative, practical solutions that make a measurable impact, we encourage you to apply!

Work you'll do

As a Manager on the Life Sciences team, you will be responsible for:

  • Leading workstreams for Veeva Vault-enabled transformation programs across regulatory, clinical, quality, or safety functions
  • Managing project plans, deliverables, risks, issues, and stakeholder communications across client and Deloitte teams
  • Translating business requirements into process, data, and system design documentation to support solution delivery
  • Supporting client workshops, decision-making, and implementation activities related to regulatory operations and digital transformation
  • Coaching junior team members while contributing to quality delivery, issue resolution, and program execution

A successful candidate would possess these skills:

  • Ability to work independently and collaborate as part of a team
  • Effective written and verbal communication skills
  • Meticulous attention to detail and quality of work product
  • Ability to build and sustain professional relationships
  • Ability to lead projects or workstreams
  • Ability to manage and prioritize multiple tasks in a fast-paced and dynamic environment
  • Strong interpersonal skills and professional demeanor
  • Ability to meet deadlines
  • Ability to mentor and provide clear guidance to others

The team

Deloitte's Life Sciences practice advises pharmaceutical, biotechnology, and medical products organizations on complex regulatory, operational, and technology transformation initiatives. Our teams help clients design and implement Veeva Vault solutions across Regulatory Information Management (RIM), Clinical, Quality, and Safety, while improving regulatory processes, data structures, content management, and submission readiness. As part of this team, you would work in a consulting environment with cross-functional practitioners and client stakeholders to deliver large-scale transformation programs, guide strategic decisions, and help clients realize value from digital and AI-enabled regulatory capabilities.

Qualifications

Required:

  • Bachelor's degree
  • Experience leading or supporting Veeva Vault implementation, enhancement, or optimization projects
  • Experience serving Life Sciences clients in a consulting, regulatory, clinical, quality, or safety environment
  • Experience managing project workstreams, deliverables, risks, issues, and stakeholder communications
  • Experience gathering business requirements and translating them into process, data, or system design documentation
  • Ability to travel 50%, on average, based on the work you do and the clients and industries/sectors you serve.
  • Limited immigration sponsorship may be available.

Preferred:

  • Master's degree
  • Experience with Veeva Vault applications supporting Regulatory Information Management (RIM), Clinical, Quality, or Safety
  • Experience leading client workshops, transformation planning, or implementation activities
  • Experience with regulatory data, content, or submission processes
  • Experience supporting proposals, statements of work, or business development activities
  • Veeva Vault certification

The wage range for this role takes into account the wide range of factors that are considered in making compensation decisions including but not limited to skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Deloitte, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current range is $155,600-$306,800.

You may also be eligible to participate in a discretionary annual incentive program, subject to the rules governing the program, whereby an award, if any, depends on various factors, including, without limitation, individual and organizational performance. 


Qualifications:

Passionate about helping Life Sciences organizations navigate strategic, operational, and regulatory priorities while driving meaningful transformation? If you're excited to work across multidisciplinary teams to deliver innovative, practical solutions that make a measurable impact, we encourage you to apply!

Work you'll do

As a Manager on the Life Sciences team, you will be responsible for:

  • Leading workstreams for Veeva Vault-enabled transformation programs across regulatory, clinical, quality, or safety functions
  • Managing project plans, deliverables, risks, issues, and stakeholder communications across client and Deloitte teams
  • Translating business requirements into process, data, and system design documentation to support solution delivery
  • Supporting client workshops, decision-making, and implementation activities related to regulatory operations and digital transformation
  • Coaching junior team members while contributing to quality delivery, issue resolution, and program execution

A successful candidate would possess these skills:

  • Ability to work independently and collaborate as part of a team
  • Effective written and verbal communication skills
  • Meticulous attention to detail and quality of work product
  • Ability to build and sustain professional relationships
  • Ability to lead projects or workstreams
  • Ability to manage and prioritize multiple tasks in a fast-paced and dynamic environment
  • Strong interpersonal skills and professional demeanor
  • Ability to meet deadlines
  • Ability to mentor and provide clear guidance to others

The team

Deloitte's Life Sciences practice advises pharmaceutical, biotechnology, and medical products organizations on complex regulatory, operational, and technology transformation initiatives. Our teams help clients design and implement Veeva Vault solutions across Regulatory Information Management (RIM), Clinical, Quality, and Safety, while improving regulatory processes, data structures, content management, and submission readiness. As part of this team, you would work in a consulting environment with cross-functional practitioners and client stakeholders to deliver large-scale transformation programs, guide strategic decisions, and help clients realize value from digital and AI-enabled regulatory capabilities.

Qualifications

Required:

  • Bachelor's degree
  • Experience leading or supporting Veeva Vault implementation, enhancement, or optimization projects
  • Experience serving Life Sciences clients in a consulting, regulatory, clinical, quality, or safety environment
  • Experience managing project workstreams, deliverables, risks, issues, and stakeholder communications
  • Experience gathering business requirements and translating them into process, data, or system design documentation
  • Ability to travel 50%, on average, based on the work you do and the clients and industries/sectors you serve.
  • Limited immigration sponsorship may be available.

Preferred:

  • Master's degree
  • Experience with Veeva Vault applications supporting Regulatory Information Management (RIM), Clinical, Quality, or Safety
  • Experience leading client workshops, transformation planning, or implementation activities
  • Experience with regulatory data, content, or submission processes
  • Experience supporting proposals, statements of work, or business development activities
  • Veeva Vault certification

The wage range for this role takes into account the wide range of factors that are considered in making compensation decisions including but not limited to skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Deloitte, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current range is $155,600-$306,800.

You may also be eligible to participate in a discretionary annual incentive program, subject to the rules governing the program, whereby an award, if any, depends on various factors, including, without limitation, individual and organizational performance. 


Education:Bachelor's DegreeEmployment Type:

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