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Veeva Vault Manager Jobs in Delaware (NOW HIRING)

CEDENT

Study Start-Up Manager

Wilmington, DE · On-site

Summary We are looking for a Study Start-Up Manager with extensive experience to lead clinical ... At least 1 year of hands-on experience with Veeva Vault. * Strong background in informed consent ...

Prophecy Technologies

R&D CSV Engineer

Wilmington, DE · On-site

Manage deviations and Corrective and Preventive Actions (CAPA), ensuring full compliance with ... High-level understanding of Veeva Vault suites. * Proficiency in risk-based testing aligned to CSA ...

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Veeva Vault Manager information

What is the difference between Veeva Vault Manager vs Veeva Vault Administrator?

AspectVeeva Vault ManagerVeeva Vault Administrator
Primary RoleOversees Vault implementation, configuration, and overall managementPerforms day-to-day Vault maintenance, user management, and support
Required SkillsTechnical knowledge of Vault, project management, and system configurationUser support, troubleshooting, and basic Vault configuration
Work EnvironmentTypically in a project or technical team setting within life sciences companiesSupport teams or IT departments managing Vault systems

Veeva Vault Managers focus on strategic management and configuration of Vault systems, while Vault Administrators handle daily operations and user support. Both roles are essential in life sciences companies using Veeva Vault, but the Manager role involves more technical and project oversight responsibilities.

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What cities in Delaware are hiring for Veeva Vault Manager jobs?

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Study Start-Up Manager

CEDENT

Wilmington, DE • On-site

Full-time

Re-posted 26 days ago

Job description

Summary

We are looking for a Study Start-Up Manager with extensive experience to lead clinical study start-up activities. This role requires a strong background in regulatory processes, site management, and expertise in ensuring compliance with local and international guidelines, particularly ICH-GCP.
 

Key Responsibilities
  • Lead and manage start-up activities for clinical studies, ensuring compliance with local and international guidelines (ICH-GCP).
  • Prepare, review, and track site regulatory documentation throughout the study start-up phase.
  • Collaborate with Clinical Research Associates (CRAs) and the local study team to meet start-up milestones.
  • Participate in Local Study Team meetings and report on site performance metrics.
  • Ensure the timely submission of documents to regulatory authorities and maintain the trial master file (eTMF).

Qualifications
  • Minimum 3 years of experience in Clinical Study Start-Up (full-time).
  • At least 1 year of hands-on experience with Veeva Vault.
  • Strong background in informed consent review and negotiation.
  • Bachelor’s degree (higher degree preferred) with knowledge of clinical trial processes (Phases II-IV) and ICH-GCP.
  • Excellent communication, organizational, and project management skills.
  • Strong problem-solving and negotiation abilities.
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About Cedent

Sourced by ZipRecruiter

CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008

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