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Veeva Clinical Jobs in Oak Ridge, NJ (NOW HIRING)

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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 the key skills and qualifications needed to thrive as a Veeva Clinical specialist?

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.

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 cities near Oak Ridge, NJ are hiring for Veeva Clinical jobs?

Cities near Oak Ridge, NJ with the most Veeva Clinical job openings:

Veeva Clinical jobs near you
Infographic showing various Veeva Clinical job openings in Oak Ridge, NJ as of June 2026, with employment types broken down into 4% As Needed, 69% Full Time, 20% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.

Analytical Science Manager

System One

Parsippany, NJ • On-site

$100K - $135K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 13 days ago

Job description

Job Title: Analytical Science Manager Location: Parsippany, NJ Type: Direct Hire - Full time permanent Compensation: $100,000.00 - $135,000.00 Work Model: Hybrid – 2 days onsite, 3 days work from home Responsibilities

  • Lead analytical method transfers and validation activities for drug substance and drug products.
  • Author and review GMP documents such as SOPs, protocols, summary reports, and QMS records.
  • Partner with Quality Assurance, Regulatory Affairs, and external test sites to support technology transfers, and analytical method validations.
  • Support technical investigations for out-of-specification (OOS) results and collaborate with QA to implement corrective actions.
  • Serve as department Quality liaison and utilize Veeva eQMS to manage documents, deviations, change controls and quality events.
Requirements
  • In-depth knowledge of analytical instrumentation (HPLC, GC, LC-MS), and physical characterization techniques (XRPD, DSC).
  • Strong troubleshooting capabilities to resolve complex analytical failures and instrument issues.
  • Thorough understanding of global regulatory mandates, including ICH guidelines, cGMP regulations, and industry best practices.
  • Strong collaboration and communication skills across cross-functional and global teams.
  • Good organizational and multi-tasking skills to successfully manage completing projects.
  • Masters in Chemistry, Pharmaceutical Sciences, or related field with 5-10 years of pharmaceutical industry experience.
  • Strong expertise in analytical method validation, and global method transfers.
  • Excellent technical writing skills and ability to author regulatory documentation as required.
  • Hands-on experience with Veeva eQMS is highly preferred

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. #M- #LI- #LI-ES1 Ref: #568-Clinical

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About System One

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System One helps employers get work done more efficiently and economically without compromising quality. Over our 35+ year history, we've helped connect thousands of talented people with innovative companies. The excitement of a perfect fit motivates us every single day.

Industry

Business consulting services and recruiting and staffing services

Company size

5,001 - 10,000 Employees

Headquarters location

Pittsburgh, PA, US

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