Clinical Compliance Operations Specialist
- Employment
- Full-time
- Company size
- Enterprise
Open to IE only. Set where you work from to check your eligibility.
No BS summary
GxP compliance operations specialist for clinical/GCP support in a SaaS life‑sciences company. Remote in Ireland (Dublin) — will work with global cross‑functional teams, author GxP documents, review deliverables and conduct supplier assessments. Must be able to support GCP, HIPAA and CSV regulated domains.
Core skills
Required skills
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead.
At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors.
As a Work Anywhere company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment.
Join us in transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities.
The Role As a Clinical Compliance Operations Specialist, you will facilitate and manage GCP project implementation audits ensuring internal adherence to Veeva processes. The Clinical Compliance Operations Specialist will ensure quality processes are defined, followed, and maintained across multiple product and service lines and regulated domains (e.g., GCP, HIPAA, CSV). This role will work closely with cross-functional global teams to provide GCP support for Veeva products in varying Services areas by promoting GCP compliance, authoring GxP documents and records, reviewing project implementation deliverables, incident management review, and performing occasional supplier assessments.
What you'll do
- Facilitate and manage GCP project implementation audits ensuring internal adherence to Veeva processes.
- Ensure quality processes are defined, followed, and maintained across multiple product and service lines and regulated domains (e.g., GCP, HIPAA, CSV).
- Provide GCP support for Veeva products in varying Services areas by promoting GCP compliance.
- Author GxP documents and records.
- Review project implementation deliverables.
- Incident management review.
- Perform occasional supplier assessments.
- Work closely with cross-functional global teams.
What they require
- Experience supporting GCP, HIPAA, CSV and other regulated domains.
- Ability to author GxP documents and records.
- Experience conducting audits, reviewing deliverables and incident management.
- Experience performing supplier assessments.
- Ability to work with cross-functional global teams.
Benefits
- Work Anywhere (flexibility to work from home or in the office)
- Global company with offices in more than 15 countries
- Equal opportunity employer and disability accommodation (contact talent_accommodations@veeva.com)
Veeva Systems is building the industry cloud for Life Sciences to help companies work in a more efficient and connected way. Veeva Business Consulting focuses on making the life sciences industry more efficient and effective through software, data, and consulting working together.
What people say about this company
3.5/ 5
- Employees appreciate the company's focus on the life sciences industry and its mission.
- Many reviews mention a collaborative and supportive work culture.
- Some employees report issues with management and communication.