RTSM Biostatistician @ Veeva Systems

INACTIVE

Full-Time

RTSM Biostatistician

Posted on 3/23/2023

Veeva Systems

5,001-10,000 employees

Cloud computing services for pharmaceutical companies.

Junior

Dorchester, Boston, MA, USA

Requirements

Masters or Ph.D. in a statistical discipline (or equivalent experience)
1+ year experience within or consulting for pharmaceutical companies and/or CROs
Direct experience preparing and delivering randomization lists in the clinical space
Deep understanding of complex statistical methods that apply to clinical trials

Responsibilities

Consult with sponsors and CROs on randomization and trial supply needs
Provide biostatistical expertise to project management and validation teams throughout study design, testing, and execution
Manage the generation of randomization lists and associated specifications per study design and as required
Collaborate with product and strategy teams to identify innovative RTSM solutions and services related to biostatistical services

Desired Qualifications

Experience leading a Validation team in RTSM

Veeva [NYSE: VEEV] is the leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, our customers range from the world’s largest pharmaceutical companies to emerging biotechs. Veeva’s software helps our customers bring medicines and therapies to patients faster.

We are the first public company to become a Public Benefit Corporation. As a PBC, we are committed to making the industries we serve more productive, and we are committed to creating high-quality employment opportunities.

Veeva is a Work Anywhere company which means that you can choose to work in the environment that works best for you - on any given day. Whether you choose to work remotely from home or work in an office - it’s up to you.

The Role

Veeva Systems, a leader in cloud-based solutions for the global life sciences industry, is looking for a Biostatistician to join our RTSM (Randomization and Trial Supply Management) team. The Biostatistician will work with our sponsor and CRO customers to provide expertise and consultation on randomization best practices and create randomization lists. This is a full-time, exempt position. Work days and hours are generally Monday through Friday, 9:00 AM to 5:00 PM; however, hours depend on customer needs and deliverables.

What You’ll Do

Consult with sponsors and CROs on randomization and trial supply needs
Provide biostatistical expertise to project management and validation teams throughout study design, testing, and execution
Manage the generation of randomization lists and associated specifications per study design and as required
Collaborate with product and strategy teams to identify innovative RTSM solutions and services related to biostatistical services

Requirements

Masters or Ph.D. in a statistical discipline (or equivalent experience)
1+ year experience within or consulting for pharmaceutical companies and/or CROs
Direct experience preparing and delivering randomization lists in the clinical space
Deep understanding of complex statistical methods that apply to clinical trials

Nice to Have

Experience leading a Validation team in RTSM

#LI-RemoteUS

#BI-Remote

Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.

Veeva is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances. If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at [email protected]. Position may not be eligible for remote work in Colorado.

Veeva Systems

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Veep's mission is to help R&D, quality, and regulatory teams eliminate inefficiencies and bring high-quality, safe, sustainable products to market without compromising quality. The company builds cloud-based tools for pharmaceutical research.

Company Stage

IPO

Total Funding

$224M

Headquarters

Pleasanton, California

Founded

2007

Growth & Insights

Headcount

6 month growth

↑ 4%

1 year growth

↑ 22%

2 year growth

↑ 39%

Benefits

Parental leave

PTO

Free food

Health, dental, & vision insurance

Gym membership reimbursement

INACTIVE