Senior Business Consultant - Life Sciences R&D

Veeva Systems Inc.Massachusetts - Boston

Hybrid Full-time

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Experience Level

Senior

Qualifications

To excel in this role, candidates should possess a strong background in life sciences, regulatory affairs, or a related field. Proven experience in managing consulting projects and engaging with senior stakeholders is crucial. The ability to analyze complex problems, craft actionable solutions, and maintain effective communication with various stakeholders will be essential for success.

About the job

At Veeva, our core values are paramount: Do the Right Thing, Customer Success, Employee Success, and Speed. We are more than just a public company; in 2021, we made history by becoming a public benefit corporation (PBC), committed to balancing the interests of our customers, employees, society, and investors.

Embracing flexibility, we are a Work Anywhere company, allowing you to choose where you thrive best, whether that be at home or in the office.

Join us in transforming the life sciences industry and making a meaningful impact on our customers, employees, and communities.

The Role

We are on the lookout for exceptional talent to join the Veeva Business Consulting group focused on R&D, a strategic priority for us. We partner with senior stakeholders from 85% of the top 20 pharmaceutical companies to define and unlock the strategic value of Regulatory Affairs, Clinical Strategy & Operations, as well as Quality and Safety (e.g., Pharmacovigilance).

In your role as a Senior Consultant, you will lead complex consulting projects tailored for Veeva's clients in the R&D sector. This includes managing teams and overseeing all aspects of project delivery. You will tackle intriguing challenges, develop innovative solutions, and foster strong relationships with stakeholders to deliver tangible value, remaining at the cutting edge of digital transformation and R&D innovation.

About Veeva Systems Inc.

Veeva Systems Inc. is at the forefront of cloud technology for the life sciences industry, enabling companies to streamline processes and enhance patient outcomes. With a commitment to social responsibility and innovation, Veeva continues to lead the way in transforming how the industry operates.

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Nov 14, 2022

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Senior Business Consultant - Life Sciences R&D

Veeva Systems Inc.

Full-time|Hybrid|Massachusetts - Boston

Veeva Systems Inc. is a purpose-driven leader in the industry cloud space, dedicated to accelerating the delivery of therapies to patients within the life sciences sector. As one of the fastest-growing SaaS companies ever, we achieved over $2 billion in revenue in our last fiscal year and are poised for continued growth.At Veeva, our core values are paramount: Do the Right Thing, Customer Success, Employee Success, and Speed. We are more than just a public company; in 2021, we made history by becoming a public benefit corporation (PBC), committed to balancing the interests of our customers, employees, society, and investors.Embracing flexibility, we are a Work Anywhere company, allowing you to choose where you thrive best, whether that be at home or in the office.Join us in transforming the life sciences industry and making a meaningful impact on our customers, employees, and communities.The RoleWe are on the lookout for exceptional talent to join the Veeva Business Consulting group focused on R&D, a strategic priority for us. We partner with senior stakeholders from 85% of the top 20 pharmaceutical companies to define and unlock the strategic value of Regulatory Affairs, Clinical Strategy & Operations, as well as Quality and Safety (e.g., Pharmacovigilance).In your role as a Senior Consultant, you will lead complex consulting projects tailored for Veeva's clients in the R&D sector. This includes managing teams and overseeing all aspects of project delivery. You will tackle intriguing challenges, develop innovative solutions, and foster strong relationships with stakeholders to deliver tangible value, remaining at the cutting edge of digital transformation and R&D innovation.

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Business Consultant - Life Sciences Research & Development

Veeva Systems Inc.

Full-time|Hybrid|Massachusetts - Boston

Veeva Systems is a purpose-driven organization and a leader in the industry cloud sector, dedicated to accelerating the delivery of therapies to patients in the life sciences sector. As one of the fastest-growing SaaS companies in history, we achieved over $2 billion in revenue in our last fiscal year, with significant growth opportunities on the horizon.Central to Veeva's mission are our core values: Doing the Right Thing, Ensuring Customer Success, Fostering Employee Success, and Promoting Speed. We are not just another public company; we made history in 2021 by becoming a public benefit corporation (PBC), which legally obliges us to balance the interests of our customers, employees, society, and investors.As a Work Anywhere company, we offer the flexibility to work from home or in the office, empowering you to thrive in your optimal work environment.Join us in transforming the life sciences industry, as we remain committed to making a positive impact on our customers, employees, and the communities we serve.Role OverviewWe are on the lookout for exceptional talent to join our Business Consulting group within R&D, a vital focus area for Veeva. We collaborate with senior customer stakeholders, recognized as the partner of choice for 85% of the top 20 pharmaceutical companies, to define and capture the strategic value of Regulatory Affairs, Clinical Strategy & Operations, as well as Quality and Safety (e.g., Pharmacovigilance). As a Consultant, you will oversee consulting project workstreams for Veeva's R&D customers, orchestrating planning, organization, and tracking of all delivery aspects. You will engage in problem analysis, develop insightful solutions, and cultivate strong relationships with customer stakeholders through various channels (in-person meetings, workshops, email, etc.) to deliver measurable and sustainable value, at the forefront of digital and R&D innovation.

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Mar 21, 2023

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Full-time|On-site|Boston, Massachusetts, United States

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Feb 27, 2026

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Apr 3, 2026

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Director of Clinical Operations

Avalyn Pharma

Full-time|$215K/yr - $230K/yr|Remote|Boston, MA

Company Overview Avalyn Pharma is innovating the landscape of pulmonary fibrosis treatment through a groundbreaking pipeline of inhaled formulations. These approved medications are expertly designed to minimize systemic exposure and deliver targeted therapy directly to the affected areas. Pulmonary fibrosis, characterized by lung tissue scarring, diminishes lung function and quality of life, contributing to increased mortality rates. Conventional therapeutic options may slow disease progression but often come with significant toxicities that limit their application. Avalyn’s inhaled approach directly addresses the underlying causes of pulmonary fibrosis, aiming to enhance patient outcomes with reduced systemic side effects. Currently, Avalyn’s AP01, an optimized inhaled formulation of pirfenidone, is under investigation in the MIST Phase 2b study for progressive pulmonary fibrosis (PPF). This formulation has demonstrated clinical proof-of-concept with better efficacy and safety profiles compared to existing treatments, having been evaluated in over 150 patients with various forms of pulmonary fibrosis. Furthermore, Avalyn has completed two Phase 1 studies for AP02, an inhaled formulation of nintedanib for idiopathic pulmonary fibrosis (IPF), with plans for a Phase 2 clinical trial in the works. For more details, please visit avalynpharma.com and follow us on LinkedIn.

Apr 3, 2026

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Associate Business Consultant - Life Sciences Commercial

Veeva Systems Inc.

Full-time|On-site|Massachusetts - Boston

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Oct 12, 2021

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Regional Clinical Trial Manager - East Coast, US

Prilenia

Full-time|On-site|Boston, MA

About PrileniaPrilenia is an innovative biopharmaceutical company dedicated to delivering groundbreaking therapies for individuals impacted by severe neurodegenerative diseases. Our global team is passionate and committed to advancing medical science, particularly through our development of pridopidine, an oral investigational neuroprotective treatment targeting ALS and Huntington’s disease (HD). Collaborating with Ferrer, we are poised to initiate critical late-stage trials that may lead to global approval for ALS and HD by the first half of 2026. Role OverviewWe are on the lookout for a motivated Regional Clinical Trial Manager to join our expanding team. This pivotal role involves overseeing and managing the operational activities of global pivotal trials in neurodegeneration. The successful candidate will possess extensive clinical research experience, particularly in clinical project management, and will have a proven track record of successfully managing global pivotal clinical trials for biotech sponsors. Experience with rare diseases, particularly ALS or HD, is highly desirable. This position requires a self-starter who can work independently across multiple projects while effectively collaborating within a matrix global team environment. The Regional Clinical Trial Manager will report directly to the SVP, Head of Clinical Operations.

Mar 12, 2026

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Full-time|Remote|Boston, Massachusetts

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Jan 15, 2025

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Corporate Counsel - Commercial

Axon Enterprise, Inc.

Full-time|$112.5K/yr - $180K/yr|On-site|Boston, Massachusetts, United States

Axon’s legal team works to support the company’s mission to protect life by building devices and cloud solutions for safety and justice. Collaboration shapes daily work, with team members sharing ideas, listening to different perspectives, and connecting with customers and communities. Role overview The Corporate Counsel - Commercial joins Axon’s contracts and corporate group, focusing on global sales operations. This attorney works closely with teams across Sales, Supply Chain, Software and Hardware Engineering, Product, and IT. The position centers on negotiating complex agreements and improving processes that help Axon scale quickly. Location Boston, MA Scottsdale, AZ Atlanta, GA Reporting This position reports to the Vice President, Corporate, Commercial & Privacy Legal.

Apr 24, 2026

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