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Veeva Clinical Jobs in Minnesota (NOW HIRING)

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?

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 popular job titles related to Veeva Clinical jobs in Minnesota?

For Veeva Clinical jobs in Minnesota, the most frequently searched job titles are:

What cities in Minnesota are hiring for Veeva Clinical jobs?

Cities in Minnesota with the most Veeva Clinical job openings:

Senior Consultant - MedTech QMS Complaints

Veeva Systems, Inc.

Minneapolis, MN • On-site

$80 - $200/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 days ago


Veeva Systems rating

7.6

Company rating: 7.6 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

154th of 244 rated software companies


Job description

The Role

Veeva is looking for an experienced consultant to lead MedTech Complaints implementations at Veeva’s MedTech customers globally. This role will guide the transformation of our customers’ Complaints Management processes and technology. The MedTech Complaints consultant will work closely with Professional Services teams to ensure delivery success across QMS implementations.

What You'll Do
  • Review and analyze existing Customer business process and identify key process steps, gaps, and requirements that would impact implementation approach
  • Lead QMS Complaints implementation workstreams at our customers for Veeva’s MedTech Quality Management solutions
  • Function as a Primary customer liaison managing communication between implementation teams, customer stakeholders, and 3rd parties
  • Analyze customer requirements and new product features to develop customer adoption and enhancement roadmaps
  • Guide customers in adopting Vault and industry best practices as part of post-implementation programs focused on the holistic success and continuous improvement of the customer
Requirements
  • 8+ years of experience in GMP Systems ownership or Software Consulting
  • 5+ years of experience in Complaints Management for Medical Device
  • Strong understanding of FDA, EU MDR/IVDR requirements and Reporting
  • Understanding of relationship between Complaint Handling, CAPA, Nonconformance and Risk Management processes
  • Knowledge of ISO 13485 and 14971, FDA21CFR Part 803, 820, 822, 806, EU GMP Annex 11
  • Proven track record leading implementation and/or IT operations as a consultant, business analyst, or IT lead and/or business sponsor
  • Proven ability to work both independently and in teams in a dynamic, fast-moving environment
  • Good understanding of SaaS and GxP principles
  • Ability to quickly understand business requirements and design creative solutions
  • Excellent verbal and written communication skills
  • Experience in the Life Sciences Quality, Manufacturing, or Healthcare spaces
  • Experience with Data or Content Management applications
Nice to Have
  • Veeva Vault implementation experience
  • Management Consulting
  • Change Management experienceField Action and Product Return experience
  • Clinical Medical Device, Biologics, and SaMD experience
Perks & Benefits
  • Medical, dental, vision, and basic life insurance
  • Flexible PTO and company paid holidays
  • Retirement programs
  • 1% charitable giving program
Compensation
  • Base pay: $80,000 - $200,000
  • The salary range listed here has been provided to comply with local regulations and represents a potential base salary range for this role. Please note that actual salaries may vary within the range above or below, depending on experience and location. We look at compensation for each individual and base our offer on your unique qualifications, experience, and expected contributions. This position may also be eligible for other types of compensation in addition to base salary, such as variable bonus and/or stock bonus.
Equal Opportunity Employer

Veeva is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances. If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at talent_accommodations@veeva.com.

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