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Full Time Regulatory Information Management Jobs

The University of Miami

Regulatory Analyst 1

Miami, FL · On-site +1

The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time ... Completion of the new protocol submission packet with the information provided by PRMC as well as ...

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How much do full time regulatory information management jobs pay per year?

As of Aug 9, 2026, the average yearly pay for full time regulatory information management in the United States is $110,733.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,500.00 and $136,500.00 per year, depending on experience, location, and employer.

What are some common challenges faced in a full time regulatory information management role, and how can they be effectively addressed?

Professionals in Regulatory Information Management often encounter challenges such as staying up-to-date with evolving global regulations, managing large volumes of complex data, and ensuring data consistency across multiple regulatory submissions. These can be effectively addressed by using robust regulatory information management systems, collaborating closely with cross-functional teams (such as regulatory affairs, IT, and quality assurance), and participating in ongoing training to remain current on industry standards. Proactive communication and a structured approach to documentation are also key to success in this role.

What is the difference between Full Time Regulatory Information Management vs Regulatory Affairs Specialist?

AspectFull Time Regulatory Information ManagementRegulatory Affairs Specialist
CredentialsTypically requires a degree in life sciences or related field, with certifications in regulatory affairs often preferredRequires a degree in life sciences, with certifications like RAC or RAPS often preferred
Work EnvironmentFocuses on managing regulatory data, documentation, and compliance systems within pharmaceutical or biotech companiesInvolves preparing and submitting regulatory documents, liaising with authorities, and ensuring product compliance
Industry UsageCommonly used in pharmaceutical, biotech, and medical device industries for data management rolesUsed across similar industries for roles involving regulatory submissions and compliance

Full Time Regulatory Information Management primarily handles the organization and maintenance of regulatory data and documentation, ensuring compliance through data systems. In contrast, Regulatory Affairs Specialists focus on preparing submissions and liaising with regulatory agencies. Both roles are essential in the regulatory process but differ in scope and daily responsibilities.

What are the key skills and qualifications needed to thrive as a full time regulatory information management professional, and why are they important?

To thrive as a Full Time Regulatory Information Management professional, you need expertise in regulatory affairs, data management, and a strong understanding of industry regulations, often supported by a degree in life sciences or a related field. Familiarity with regulatory information management systems (RIMS), electronic document management systems (EDMS), and relevant certifications such as RAC (Regulatory Affairs Certification) are typically required. Excellent organizational skills, attention to detail, and effective communication enable professionals to manage complex data and collaborate with cross-functional teams. These skills are crucial to ensure regulatory compliance, streamline submissions, and support the organization’s ability to bring products to market efficiently.

What is regulatory information management?

Regulatory Information Management (RIM) is the process of collecting, organizing, and managing regulatory data and documents required for compliance with government regulations in industries such as pharmaceuticals, biotechnology, and medical devices. Professionals in RIM ensure that product information, submissions, and approvals are accurately tracked and updated to meet global regulatory requirements. This role involves working with regulatory submissions, supporting audits, and maintaining data integrity across various systems. A full-time RIM professional plays a key role in helping organizations streamline compliance processes and reduce the risk of regulatory penalties.
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What are the most commonly searched types of Regulatory Information Management jobs? The most popular types of Regulatory Information Management jobs are:
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Full Time Regulatory Information Management jobs near you
Infographic showing various Full Time Regulatory Information Management job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $110,733 per year, or $53.2 per hour.

Senior Consultant- Clinical & Regulatory Information Management

NNIT

Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 28 days ago

Job description

Senior Consultant- Clinical & Regulatory Information Management
US
Apply now
Details
Type of contract:Full Time
Location(s): US
Language(s):English
Mobility:n/a
Application Deadline:
NNIT is seeking a highly motivated Clinical / Regulatory Information Management (RIM) Subject Matter Expert (SME) to support and expand our growing Veeva Technology Practice. This role will serve as a cross-functional business and technology resource, supporting multiple client delivery of PODs across Veeva RIM and adjacent Clinical and Regulatory initiatives.
The ideal candidate combines a strong understanding of Life Sciences business processes with hands-on experience in Veeva Vault applications, requirements gathering, process optimization, and implementation readiness activities. This individual will help bridge the gap between business stakeholders and technical delivery teams while supporting both implementation and Managed Services engagements.
Duties and Responsibilities:
Serve as a functional SME for Veeva Vault RIM and related Clinical/Regulatory business processes.
Lead or support business process discovery, current-state/future-state assessments, and gap analysis workshops.
Gather, analyze, and document business, functional, and technical requirements.
Develop process maps, workflow designs, user stories, and business rules to support Veeva implementations.
Partner with Veeva delivery teams, client stakeholders, and NNIT technical consultants to accelerate project readiness.
Support Phase 0 assessments and implementation planning activities, including governance, data readiness, and operating model design.
Assist with data migration readiness, role and permission matrix development, and validation planning.
Contribute to User Acceptance Testing (UAT), requirements traceability, and solution verification activities.
Support hypercare and Managed Services engagements by providing functional expertise, issue analysis, and continuous improvement recommendations.
Help develop reusable accelerators, templates, playbooks, and best practices that can be leveraged across multiple client engagements.
Strategic Value:
This role is foundational to NNIT's strategy of providing end-to-end support across the Veeva lifecycle:
Strategy → Phase 0 Readiness → Implementation → Hypercare → Managed Services → Continuous Improvement.
The successful candidate will play a key role in helping clients align business processes with Veeva best practices while enabling faster implementations, sustainable operations, and long-term customer success.
Role Within the NNIT Operating Model:
This position is designed as a flexible, cross-functional SME resource that can:
Support multiple implementation POD's simultaneously
Lead Phase 0 business and process readiness activities
Partner with Veeva and client delivery teams to accelerate implementations.
Transition into post-go-live Managed Services support and optimization activities.
Help build repeatable frameworks and scalable service offerings across the NNIT Quality & Regulatory Technology Practice.
Qualifications and Education Requirements:
5+ years of experience in Life Sciences consulting, Regulatory Affairs, Clinical Operations, or Veeva implementation projects.
Experience supporting Veeva Vault RIM, eTMF, QMS, or related Vault applications.
Familiarity with GxP environments and Computer Software Assurance (CSA) or CSV methodologies.
Experience working within global delivery models and cross-functional project teams.
Prior consulting or Managed Services experience is highly desirable.
Preferred Skills:
Strong understanding of Clinical Development and/or Regulatory Affairs processes within the Life Sciences industry.
Experience with Veeva Vault RIM (Registrations, Submissions, Submissions Archive, or Publishing) preferred.
Experience working with Veeva Vault platform implementations or support engagements.
Ability to facilitate workshops and communicate effectively with business and technical stakeholders.
Experience documenting business requirements, process flows, user stories, and functional specifications.
Familiarity with data migration, validation, UAT, and change management activities.
Understanding of regulatory submissions, product registrations, document management, or end-to-end regulatory operations.
Strong analytical, communication, and organizational skills with a consultative mindset.
Benefits:NNIT Offers a comprehensive benefits package including:
Competitive Salary
Medical, Dental, Vision Insurance
401K
Paid Holidays
Annual Paid Time Off
Salary:
Dependent upon Experience
Additional Notes:
You will be part of a dedicated, international, and professional team in NNIT's research and development department working closely with the Associate Vice President of the department. As a member of our team, you can count on challenges and development in an attractive and professional setting.
Candidates must be legally authorized to work in the U.S. without requiring current or future visa sponsorship.
About NNIT
NNIT is a public listed company who specializes in IT solutions to life sciences internationally, and to the public and enterprise sectors in Denmark. We focus on high complexity industries and thrive in environments where regulatory demands and complexity are high. We advise on and build sustainable digital solutions that work for the patients, citizens, employees, end users or customers. NNIT consists of group company NNIT A/S and subsidiaries SCALES, Excellis Health Solutions and SL Controls. Together, these companies employ more than 1,800 people in Europe, Asia, and USA.
We celebrate diversity and are committed to creating an inclusive environment for all employees. All candidates are encouraged to apply for the given job regardless of their gender, age, religious beliefs, sexual orientation, national and social origin, political opinion, disability, race, skin colour, and ethnic origin.
In the interest of fostering a fair and unbiased recruitment process, we kindly request candidates to refrain from including their pictures in their applications.
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