← Back to jobs
Full-time

Associate Consultant - Entry-Level Technology Consulting (Life Sciences)

$80K/yr – $80K/yr

New York, NYScience & PharmaceuticalPosted yesterday

You'll complete your application on the employer's website.

Role overview

Job description

Associate Consultant - Entry-Level Technology Consulting (Life Sciences) jobs in United States

Tags

< 25 applicants

Original Job Post

Veeva Systems

$80K/yr - $80K/yr

0–2 years exp

79

GOOD MATCH

Experience Level

Skill

50

Industry Exp.

69

Responsibilities

Work directly with customers to innovate with our technology and improve their business operations

Be hands-on and become the experts on Veeva’s technology – set up and tailor our software to solve our customers’ unique business challenges

Partner with project teams and customers through problem-solving, solution design, workshops, and project management

Benefits

After one year, if you perform well, you will receive a compensation increase and participate in our bonus program

Veeva is a Work Anywhere company. You can choose to work in an office or remotely from home on any given day of the week.

Associate Consultants must live within a maximum commuting distance of 45 minutes to 1 hour from Veeva’s Boston, New York City or Madison office and typically go to the office two to three days per week.

Glassdoor

3.5

Life sciences industry cloud software, AI, data, and consulting.

Pleasanton, California, USA

http://www.veeva.com

Public Company

Total Funding

$7M

Key Investors

Emergence Capital

2013-10-16

IPO

2008-06-05

Series Unknown· $4M

2007-02-06

Angel· $3M

Leadership Team

Peter Gassner

Founder and CEO

Jim Munz

Chief Technology Officer - Digital Trials

Recent News

The Motley Fool

Flying Cars, Smart Homes, and Cracks in the AI Boom

2026-10-25

PR Newswire UK

IQVIA Selects Veeva Clinical Operations Applications

Qualifications

Drive: Thrive in a challenging, intense environment that rewards initiative and rapid learning

Curiosity: Desire to be hands-on with software and master new technologies

Communication: Excellent verbal and written communication skills

Analytical Mindset: Strong critical thinking skills and proven track record of academic performance in any major

Integrity: Veeva is a Public Benefit Corporation (PBC) and a 'do the right thing' company and we expect that from all employees

Work Ethic: A commitment to excellence and passion for working hard to achieve results

Travel: Willingness to travel as needed (up to 20-30% of the time)

Experience: Recent university graduate (up to 2 years postgraduate experience maximum)

Work Authorization: Qualified candidates must be legally authorized to be employed in the United States. Veeva does not provide sponsorship for employment visa status (e.g., H-1B, OPT, or TN status) for this employment position

Experience: Recent university graduate (up to 2 years postgraduate experience maximum).

Required skills

Recent university graduate, Represents the skills you have, Work authorization in US, click on the tags

Interested in this role?

Apply directly on the employer's website — it only takes a few minutes.

Similar vacancies

Other roles in New York, NY or Science & Pharmaceutical

HealthcareFull-time
San FranciscoScience & PharmaceuticalsPosted 30+ Days Ago

You will work at the cutting edge of OpenAI's robotics hardware, partnering with hardware and software teams to develop, build, test, and iterate on robotic systems. Working closely with engineers, you will build prototypes, execute experiments, fabricate fixtures, troubleshoot hardware, and help drive rapid iteration…

HealthcareFull-time
USA - Torrance (205th Street)Science & PharmaceuticalPosted 25d ago

When you join us, you’ll be part of a global team harnessing the power of scientific testing and data-driven insights to build a healthier future. Clinical Research Coordinator Imagine your future with us At ALS, we encourage you to dream big.

HealthcareFull-time
BIDMC East CampusScience & PharmaceuticalPosted 26d ago

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Responsible for screening research subjects for participation in clinical research projects, enrolling research subjects onto these studies, monitoring protocol implementation, completing required forms and reporting results.