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Veeva Clinical Jobs (NOW HIRING)

Lead Applications Engineer - Veeva

Concord, NC · On-site

$95K - $125K/yr

Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the ... Veeva platform architecture, configuration, and integration (required). * Software development ...

Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the ... Veeva platform architecture, configuration, and integration (required). * Software development ...

Lead Applications Engineer - Veeva

Concord, NC · On-site

$95K - $125K/yr

Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the ... Veeva platform architecture, configuration, and integration (required). * Software development ...

As a full-stack engineer, you will work with the latest technologies to contribute to the success of Veeva's clinical data platform designed for the life sciences industry and clinical trials.

They are seeking a Senior Director of Strategy to drive the adoption and growth of their Clinical Trial Management System (CTMS) within the Veeva Clinical Operations suite, focusing on market ...

Advanced knowledge of Veeva Clinical or other Clinical Trial Management Systems (CTMS) * Strong understanding of regulatory requirements and compliance in the pharmaceutical industry * Proven track ...

Advanced knowledge of Veeva Clinical or other Clinical Trial Management Systems (CTMS) * Strong understanding of regulatory requirements and compliance in the pharmaceutical industry * Proven track ...

Advanced knowledge of Veeva Clinical or other Clinical Trial Management Systems (CTMS) * Strong understanding of regulatory requirements and compliance in the pharmaceutical industry * Proven track ...

Director, Veeva Clinical CTMS Lead

Groton, CT · On-site

$79K - $108K/yr

Advanced knowledge of Veeva Clinical or other Clinical Trial Management Systems (CTMS) * Strong understanding of regulatory requirements and compliance in the pharmaceutical industry * Proven track ...

Advanced knowledge of Veeva Clinical or other Clinical Trial Management Systems (CTMS) * Strong understanding of regulatory requirements and compliance in the pharmaceutical industry * Proven track ...

Advanced knowledge of Veeva Clinical or other Clinical Trial Management Systems (CTMS) * Strong understanding of regulatory requirements and compliance in the pharmaceutical industry * Proven track ...

Advanced knowledge of Veeva Clinical or other Clinical Trial Management Systems (CTMS) * Strong understanding of regulatory requirements and compliance in the pharmaceutical industry * Proven track ...

Seeking a Veeva Vault Clinical Consultant to support system configuration and user training in clinical trial processes. Requirement/Must Have: * Hands-on experience with specific Veeva Vault modules ...

Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Description Seasoned, talented, highly experienced. Specialized in Veeva Contract Management, Event Management, and ...

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Showing results 1-20

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 June 2026, with employment types broken down into 13% Locum Tenens, 73% As Needed, 7% Temporary, and 7% Nights. Highlights an 74% Physical, 7% Hybrid, and 19% Remote job distribution.
Lead Applications Engineer - Veeva

Lead Applications Engineer - Veeva

McKesson

Concord, NC • On-site

$95K - $125K/yr

Full-time

Posted 23 days ago


McKesson rating

7.8

Company rating: 7.8 out of 10

Based on 202 frontline employees who took The Breakroom Quiz

41st of 71 rated pharmaceutical


Job description

It's More Than a Career, It's a Mission.


Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day.

Our Mission


People who live with cancer - those who work to prevent it, fight it, and survive it - are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world.

The Lead ApplicationsEngineer serves as the technical authority and solution architect for complex systems and application ecosystems. This role leads the design, integration, validation, and optimization of scalable, compliant solutions that transform manual processes into automated systems, ensuring alignment with technical, regulatory, schedule, and budgetary requirements. The Lead ApplicationsEngineer provides technical leadership across cross-functional teams, mentors engineers, and drives innovation through AI-enabled capabilities.

Key Responsibilities:

System Design & Integration:

  • Lead the deployment of enterprise and clinical engineering solutions that convert manual business processes into automated, validated systems.

  • Architect, integrate, and validate complex application ecosystems, with primary accountability for Veeva Clinical Operations and related Veeva platforms.

  • Ensure system designs meet performance, reliability, scalability, security, and regulatory requirements (e.g., GxP, Part 11).

  • Translate product and business requirements into cohesive end-to-end system solutions across multiple platforms.

  • Establish and enforce engineering standards, design patterns, and integration approaches.

  • Partner with support teams to improve reliability, monitoring, and operational maturity.

Technical Leadership:

  • Serve as the technical lead for cross-functional delivery teams, providing architectural direction and technical decision-making.

  • Mentor and develop junior and senior engineers, promoting engineering excellence, best practices, and continuous improvement.

Analysis & Problem Solving:

  • Perform functional, timeline, and trade-off analyses to evaluate solution options and recommend optimal approaches.

  • Independently resolve highly complex technical issues requiring advanced judgment, creativity, and systems thinking.

  • Balance cost, risk, supportability, and compliance in all technical decisions.

Program Management:

  • Partner with Project and Program Managers to oversee the full solution lifecycle from requirements through implementation and post-go-live support.

  • Coordinate internal and external technical resources, including vendors and platform partners.

Innovation & Development:

  • Leverage Artificial Intelligence (AI) to enhance system capabilities, automate processes, and improve decision-making.

  • Contribute to the development of innovative architectural patterns integrating AI into clinical and enterprise systems.

  • Continuously identify opportunities to apply emerging technologies to improve efficiency, scalability, and data quality.

Required Qualifications:

  • Bachelor's or Master's degree in Systems Engineering, Electrical Engineering, Computer Science, or a related field.

  • Proven experience (10+ years) in systems engineering, with a track record of leading complex projects.

  • Extensive knowledge of advanced engineering principles, theories, and concepts.

  • Strong analytical and problem-solving skills with the ability to address complex challenges.

  • Excellent leadership and communication skills, with experience mentoring and guiding teams.

  • Proficiency in system design tools and methodologies.

Skills Required:

  • Advanced application and systems engineering principles.

  • Clinical research systems and regulated environments.

  • Veeva platform architecture, configuration, and integration (required).

  • Software development lifecycle (SDLC), validation, and compliance standards.

  • Proficiency with Veeva Systems, particularly Veeva Clinical Operations (required) and Veeva Vault modules for document and regulatory management.

  • Experience with clinical system interoperability and data exchange.

  • Cloud platform experience (AWS, Azure, or GCP).

  • Agile and DevOps delivery methodologies.

  • Ability to manage multiple initiatives in a fast-paced environment.

  • Strong collaboration skills within cross-functional technical teams.

  • Solution and system architecture design.

  • Complex system integration and troubleshooting.

  • Technical leadership and mentoring.

  • Stakeholder communication and influence.

  • AI-enabled solution design and automation.

About Sarah Cannon Research Institute


Sarah Cannon Research Institute (SCRI) is one of the world's leading oncology research organizations conducting community-based clinical trials. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country. It has conducted more than 850 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA in the past decade. SCRI's research network brings together more than 1,300 physicians who are enrolling patients into clinical trials at more than 200 locations in 20+ states across the U.S. Please click here to learn more about our research offerings.
We care about the well-being of the patients and communities we serve, and that starts with caring for our people. That's why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being. Our Total Rewards offerings serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves. For more information regarding benefits through our parent company, McKesson, please click here.
As part of Total Rewards, we are proud to offer a competitive compensation package. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered.

McKesson has become aware of online recruiting-related scams in which individuals who are not affiliated with or authorized by McKesson are using McKesson's (or affiliated entities, like CoverMyMeds or RxCrossroads) name in fraudulent emails, job postings or social media messages. In light of these scams, please bear the following in mind:
McKesson Talent Advisors will never solicit money or credit card information in connection with a McKesson job application.


McKesson Talent Advisors do not communicate with candidates via online chatrooms or using email accounts such as Gmail or Hotmail. Note that McKesson does rely on a virtual assistant (Gia) for certain recruiting-related communications with candidates.

McKesson job postings are posted on our career site: careers.mckesson.com.

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.


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