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Veeva Clinical Jobs (NOW HIRING)

ImmunityBio, Inc.

Veeva RIM Specialist

Summit, NJ · On-site

Position Summary The Veeva RIM Specialist will provide expertise and guidance in the management and ... Partner with regulatory affairs, IT, and clinical teams to translate business requirements into ...

NKW NantKwest Inc

Veeva RIM Specialist

Summit, NJ

Position Summary The Veeva RIM Specialist will provide expertise and guidance in the management and ... Partner with regulatory affairs, IT, and clinical teams to translate business requirements into ...

Deloitte

Life Science Veeva Manager

Dallas, TX

Leading workstreams for Veeva Vault-enabled transformation programs across regulatory, clinical, quality, or safety functions * Managing project plans, deliverables, risks, issues, and stakeholder ...

Deloitte

Life Science Veeva Manager

Los Angeles, CA · On-site

Leading workstreams for Veeva Vault-enabled transformation programs across regulatory, clinical, quality, or safety functions * Managing project plans, deliverables, risks, issues, and stakeholder ...

Deloitte

Life Science Veeva Manager

Minneapolis, MN

Leading workstreams for Veeva Vault-enabled transformation programs across regulatory, clinical, quality, or safety functions * Managing project plans, deliverables, risks, issues, and stakeholder ...

Deloitte

Life Science Veeva Manager

Costa Mesa, CA · On-site

Leading workstreams for Veeva Vault-enabled transformation programs across regulatory, clinical, quality, or safety functions * Managing project plans, deliverables, risks, issues, and stakeholder ...

Deloitte

Life Science Veeva Manager

Washington, DC

Leading workstreams for Veeva Vault-enabled transformation programs across regulatory, clinical, quality, or safety functions * Managing project plans, deliverables, risks, issues, and stakeholder ...

Deloitte

Life Science Veeva Manager

Philadelphia, PA · On-site

Leading workstreams for Veeva Vault-enabled transformation programs across regulatory, clinical, quality, or safety functions * Managing project plans, deliverables, risks, issues, and stakeholder ...

Deloitte

Life Science Veeva Manager

Pittsburgh, PA

Leading workstreams for Veeva Vault-enabled transformation programs across regulatory, clinical, quality, or safety functions * Managing project plans, deliverables, risks, issues, and stakeholder ...

Deloitte

Life Science Veeva Manager

New York, NY

Leading workstreams for Veeva Vault-enabled transformation programs across regulatory, clinical, quality, or safety functions * Managing project plans, deliverables, risks, issues, and stakeholder ...

Deloitte

Life Science Veeva Manager

Columbus, OH

Leading workstreams for Veeva Vault-enabled transformation programs across regulatory, clinical, quality, or safety functions * Managing project plans, deliverables, risks, issues, and stakeholder ...

Deloitte

Life Science Veeva Manager

San Jose, CA

Leading workstreams for Veeva Vault-enabled transformation programs across regulatory, clinical, quality, or safety functions * Managing project plans, deliverables, risks, issues, and stakeholder ...

Deloitte

Life Science Veeva Manager

Jersey City, NJ · On-site

Leading workstreams for Veeva Vault-enabled transformation programs across regulatory, clinical, quality, or safety functions * Managing project plans, deliverables, risks, issues, and stakeholder ...

Deloitte

Life Science Veeva Manager

San Francisco, CA · On-site

Leading workstreams for Veeva Vault-enabled transformation programs across regulatory, clinical, quality, or safety functions * Managing project plans, deliverables, risks, issues, and stakeholder ...

Deloitte

Life Science Veeva Manager

Cincinnati, OH

Leading workstreams for Veeva Vault-enabled transformation programs across regulatory, clinical, quality, or safety functions * Managing project plans, deliverables, risks, issues, and stakeholder ...

Deloitte

Life Science Veeva Manager

Morristown, NJ · On-site

Leading workstreams for Veeva Vault-enabled transformation programs across regulatory, clinical, quality, or safety functions * Managing project plans, deliverables, risks, issues, and stakeholder ...

Veeva Systems

Vault Platform Pre-Sales Solution Architect

$64.50 - $85/hr

... e.g., Clinical, Regulatory, Quality) and the use of technology within these processes. (While not mandatory, it's highly advantageous given Veeva's core market) • Working knowledge of GxP ...

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Showing results 1-20

All JobsVeeva Clinical Jobs

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.
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Veeva Clinical jobs near you
Infographic showing various Veeva Clinical job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.
Director, Clinical Data Management

Director, Clinical Data Management

Syndax Pharmaceuticals

New York, NY • On-site

$220K - $250K/yr

Full-time

Posted 27 days ago

Job description

Syndax Pharmaceuticals is looking for a Director, Clinical Data Management
At Syndax, we are determined to realize a future in which people with cancer live longer and better than ever before. Syndax Pharmaceuticals is a commercial stage biopharmaceutical company developing an innovative pipeline of cancer therapies.
The Role:
This position is a strategic leader responsible for overseeing the design, implementation, and oversight of clinical data systems and processes across multiple clinical development programs. This role directs a team in delivering high-quality clinical data in alignment with regulatory requirements, corporate goals, and operational efficiency. The Director contributes to the long-term success of the function through data-driven strategies, innovation in systems and processes, and strong cross-functional partnerships. May also be responsible for projects that have been contracted with a service provider, as well as internal projects.
Key Responsibilities:
  • Collaborate with senior leadership to define and implement functional and organizational strategy aligned with corporate objectives; participate in long-term planning and policy development.
  • Development and execution of data quality strategies, risk-based data review plans, and cross-study harmonization.
  • Direct the design, testing, validation, and maintenance of clinical databases and electronic data capture (EDC) systems.
  • Ensure consistent application of CDM standards, tools (e.g., CDISC, Medidata Rave), and procedures.
  • Oversee issue resolution and data integrity across outsourced vendors and internal teams.
  • Provide proactive input into clinical protocol design to ensure data collection strategies align with scientific and regulatory requirements.
  • Review and contribute to clinical protocols and statistical analysis plans to ensure alignment with data collection objectives; cross-project consistency and standardization of case report forms.
  • Partner with internal stakeholders to align timelines and data delivery requirements.
  • Participate in cross-functional study teams; influence protocol design, study setup, and data strategy from study start to submission.
  • Actively support submission readiness, including data integration and final deliverables for regulatory filings.
  • Participate in protocol development, clinical study reports (CSR), and submission activities.
  • Manage relationships with CROs and third-party vendors, ensuring alignment with contractual deliverables and performance expectations.
  • Establish standards and oversight processes for EDC setup, CRF development, data validation, discrepancy management, and database lock.
  • Drive consistency and scalability through implementation of standards (e.g., CDISC/CDASH/SDTM) and SOPs.
  • Development and improvement of clinical data management processes and tools.
  • Lead and mentor Clinical Data Managers; provide coaching and foster a high-performing and collaborative environment.
  • Participates in the evaluation of organizational needs, defining resource strategies, and managing departmental budgets and headcount planning.

Desired Experience/Education and Personal Attributes:
  • Bachelor's degree in related scientific discipline; advanced degree preferred.
  • 12+ years of progressive experience in clinical data management with leadership responsibility at a sponsor organization.
  • Expert knowledge of clinical data management.
  • Deep expertise of industry standards including CDISC/CDASH, SDTM, ICH-GCP, 21 CFR Part 11, and regulatory submission requirements.
  • Proven success leading large-scale global studies, vendor oversight and working in both in-house and outsourced models.
  • Expertise knowledge and hands on experience with EDC systems (e.g., Medidata Rave, Veeva), clinical systems integration, and risk-based monitoring frameworks required.
  • Exceptional leadership, analytical, and communication skills with the ability to influence senior stakeholders and executives.

Location: Syndax's corporate office is in New York, NY.
Syndax offers a total compensation and rewards package that is among the most competitive in the industry. Base pay is just one element of our package and is determined within a range based on several factors including market data, experience, qualifications, demonstrated skills, relevant education or training, travel requirements and internal equity. Our overall package also includes an equity offering, annual target bonuses, and an outstanding benefits program. The anticipated annualized salary range for this role is: $220,000 - 250,000.
About Syndax:
Syndax Pharmaceuticals is a commercial-stage biopharmaceutical company advancing innovative cancer therapies. Highlights of the Company's pipeline include a menin inhibitor for R/R acute leukemia and a monoclonal antibody that blocks the CSF-1 receptor for chronic graft-versus-host disease. Fueled by our commitment to reimagining cancer care, Syndax is working to unlock the full potential of its pipeline and is conducting several clinical trials across the continuum of treatment. For more information, please visit www.syndax.com/ or follow the Company on X and LinkedIn.
Syndax Pharmaceuticals is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.
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