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Veeva Vault Edc Jobs (NOW HIRING)

Ardelyx

Clinical Trial Manager

Newark, CA · On-site +1

$136K - $160K/yr

Experience with clinical trial systems and tools including EDC, IRT and Veeva Vault platforms,) * Ability to travel occasionally to clinical sites, investigator meetings, and professional conferences ...

Ardelyx

Clinical Trial Manager

Newark, CA · On-site +1

$136K - $160K/yr

Experience with clinical trial systems and tools including EDC, IRT and Veeva Vault platforms,) * Ability to travel occasionally to clinical sites, investigator meetings, and professional conferences ...

Ardelyx

Clinical Trial Manager

Newark, CA · On-site

$136K - $160K/yr

Experience with clinical trial systems and tools including EDC, IRT and Veeva Vault platforms,) * Ability to travel occasionally to clinical sites, investigator meetings, and professional conferences ...

Ardelyx

Clinical Trial Manager

Waltham, MA · On-site +1

$136K - $160K/yr

Experience with clinical trial systems and tools including EDC, IRT and Veeva Vault platforms,) * Ability to travel occasionally to clinical sites, investigator meetings, and professional conferences ...

Ardelyx

Clinical Trial Manager

Waltham, MA · On-site +1

$136K - $160K/yr

Experience with clinical trial systems and tools including EDC, IRT and Veeva Vault platforms,) * Ability to travel occasionally to clinical sites, investigator meetings, and professional conferences ...

Ardelyx

Clinical Trial Manager

Newark, CA · On-site +1

Experience with clinical trial systems and tools including EDC, IRT and Veeva Vault platforms,) * Ability to travel occasionally to clinical sites, investigator meetings, and professional conferences ...

Ardelyx

Clinical Trial Manager

Waltham, MA · On-site +1

Experience with clinical trial systems and tools including EDC, IRT and Veeva Vault platforms,) * Ability to travel occasionally to clinical sites, investigator meetings, and professional conferences ...

Ardelyx

Clinical Trial Manager

Newark, CA · On-site +1

$136K - $160K/yr

Experience with clinical trial systems and tools including EDC, IRT and Veeva Vault platforms,) * Ability to travel occasionally to clinical sites, investigator meetings, and professional conferences ...

Ardelyx

Clinical Trial Manager

Waltham, MA · On-site +1

$136K - $160K/yr

Experience with clinical trial systems and tools including EDC, IRT and Veeva Vault platforms,) * Ability to travel occasionally to clinical sites, investigator meetings, and professional conferences ...

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Veeva Vault Edc information

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How much do veeva vault edc jobs pay per hour?

As of Jun 18, 2026, the average hourly pay for veeva vault edc in the United States is $16.77, according to ZipRecruiter salary data. Most workers in this role earn between $15.38 and $17.79 per hour, depending on experience, location, and employer.

What are some common challenges faced by professionals working with Veeva Vault EDC, and how can they be addressed?

Professionals working with Veeva Vault EDC often encounter challenges such as adapting to frequent software updates, ensuring data integrity across multiple studies, and coordinating with cross-functional teams like data management and clinical operations. Staying current with Veeva's platform enhancements and participating in ongoing training can help address these challenges. Additionally, effective communication with stakeholders and adopting best practices for data entry and validation are key to maintaining data quality and smooth study execution.

What are the key skills and qualifications needed to thrive as a Veeva Vault EDC Specialist, and why are they important?

To thrive as a Veeva Vault EDC Specialist, you generally need a strong background in clinical data management, understanding of electronic data capture (EDC) processes, and a relevant degree in life sciences or information technology. Proficiency with Veeva Vault EDC software, knowledge of GxP compliance, and certifications such as Veeva Vault Administrator or Clinical Data Management are typically required. Excellent problem-solving, communication, and attention to detail are crucial soft skills for collaborating with cross-functional teams and ensuring data quality. These skills are vital for maintaining regulatory compliance, ensuring accurate data collection, and supporting efficient clinical trial operations.

What is Veeva Vault EDC?

Veeva Vault EDC is a cloud-based electronic data capture (EDC) system used primarily in clinical trials to collect, manage, and store clinical data. It streamlines data entry and monitoring, offering tools for data validation, query management, and real-time reporting. The platform is designed to improve data quality, reduce study timelines, and ensure regulatory compliance. Veeva Vault EDC is widely used by pharmaceutical companies, contract research organizations, and other life sciences organizations to facilitate efficient and secure clinical research.
Infographic showing various Veeva Vault Edc job openings in the United States as of June 2026, with employment types broken down into 83% Full Time, and 17% Contract. Highlights an 74% Physical, 7% Hybrid, and 19% Remote job distribution, with an average salary of $34,883 per year, or $16.8 per hour.
Clinical Trial Manager

Clinical Trial Manager

Ardelyx

Newark, CA • On-site, Remote

$136K - $160K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 23 days ago

Job description

Ardelyx is a commercial-stage biopharmaceutical company focused on redefining treatment approaches for patients with significant unmet medical needs. By combining scientific innovation with a collaborative, purpose-driven culture, we strive to create meaningful impact for patients.
Team Ardelyx is united by a shared mission and guided by our core values: Passionate, Fearless, Dedicated, and Inclusive.
We foster an inclusive environment where employees are respected, supported, and empowered to make an impact - both within our company and in the lives of patients we serve.

Position Summary (Hybrid Location):

The Clinical Trial Manager (CTM) is responsible for the end-to-end operational oversight of clinical trials, from study planning through close-out and reporting. This role ensures trials are executed ethically, on time, within budget, and in full compliance with applicable regulatory requirements and Good Clinical Practice (GCP), while maintaining the highest standards of patient safety and data integrity.
Responsibilities:
  • Provide operational leadership for one or more clinical studies or programs, overseeing execution from initial study synopsis through final deliverables, including study start-up, enrollment, conduct, database lock, statistical outputs (TLFs), and Clinical Study Report (CSR)
  • Lead study start-up activities in collaboration with CROs and investigational sites, including oversight of clinical document development and site activation activities
  • Manage day-to-day study execution, ensuring adherence to timelines, milestones, budgets and quality standards
  • Contribute to and review study plans, timelines, and operational deliverables; proactively identify risks and implement mitigation strategies to ensure successful study outcomes
  • Prepare, review and/approve study-related documents including but not limited toInformed Consent Forms, CRFs, Monitoring Plans, Laboratory Manuals, Patient Diaries, Clinical Site Procedures Manual and CRF Completion Guidelines)
  • Implement risk management and mitigation strategies, prioritizing tasks and issues to ensure successful program/study objectives
  • Participate in and support user acceptance testing (UAT) for clinical systems, (e.g., EDC IRT), including contribution to system requirements and validation activities
  • Oversee vendor performance and relationships including CROs, central laboratories, and contribute to or lead the systems set-up/management, EDC/IRT, and specialty services (ePRO, ECG, imaging etc.)
  • Ensure compliance with GCP, applicable regulations, SOPs, and study-specific procedures throughout the trial lifecycle
  • Track, analyze and communicate study progress, risks and key metrics to the Study Lead and senior management, including development and maintenance dashboards and trackers
  • Represent Clinical Operations professionally, fostering productive relationships with investigators, CRO partners, vendors and internal cross functional teams
Qualifications:
  • Bachelor's degree in Life Sciences, Nursing, or a related field with 5+ years of experience in clinical trial management or related clinical research roles; equivalent experience may be considered
  • Master's degree and clinical research certification (e.g., CCRA, CCRP) strongly preferred
  • Demonstrated knowledge of current clinical trial processes, GCP, ICH guidelines and regulatory requirements
  • Strong project management skills, including managing of timelines, budgets, and cross-functional resources
  • Excellent written and verbal communication with the ability to lead cross-functional teams and external partners.
  • Proven problem-solving skills and tools, and ability to manage complex operational issues in a fast paced environment
  • Experience with clinical trial systems and tools including EDC, IRT and Veeva Vault platforms,)
  • Ability to travel occasionally to clinical sites, investigator meetings, and professional conferences as required
  • Remote work considered; preference for candidates able to attend the office weekly (Newark or Waltham)
The anticipated annualized base pay range for this full-time position is $136,000-$160,000. Ardelyx utilizes industry data to ensure that our compensation is competitive and aligned with our industry peers. Actual base pay will be determined based on a variety of factors, including years of relevant experience, training, qualifications, and internal equity. The compensation package may also include an annual bonus target and equity awards, subject to eligibility and other requirements.
Ardelyx also offers a robust benefits package to employees, including a 401(k) plan with generous employer match, 12 weeks of paid parental leave, up to 12 weeks of living organ and bone marrow leave, equity incentive plans, health plans (medical, prescription drug, dental, and vision),life insurance and disability, flexible time off, annual Winter Holiday shut down, and at least 11 paid holidays.
Ardelyx is an equal opportunity employer.
Employment Type: Full-Time

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