Life Science Jobs at Velocity Clinical Research | Apply Now
Looking to build a long-term Clinical Research Career in a regulated, patient-focused environment? Velocity Clinical Research is hiring a Regulatory Specialist I, offering a strong entry point into high-impact Life Science Jobs. This opportunity under Velocity Careers is ideal for candidates who want hands-on exposure to IRB submissions, regulatory compliance, and clinical trial operations at an integrated research site organization.
- Job Title: Regulatory Specialist I
- Employment Type: Regular, Full-Time
- Job ID: 2026-3303
About the Company
Velocity Clinical Research is an owned and integrated research site organization committed to excellence in patient care and high-quality clinical data generation. The organization supports innovative medical treatments by conducting efficient, compliant, and patient-centric clinical trials. Velocity emphasizes employee growth, performance-based rewards, and long-term career development. With a strong compliance culture and integrated operations, Velocity provides an ideal environment to grow a sustainable Clinical Research Career.
Key Responsibilities
- Prepare study-specific regulatory documents for IRB review
- Support initial IRB and sponsor submissions for study start-up
- Submit amendments, continuing reviews, deviations, and adverse event reports
- Maintain regulatory binders ensuring audit readiness
- Support SAE and AE submissions to IRBs in a timely manner
- Assist with monitoring visits, sponsor audits, and regulatory inspections
- Track training documentation and delegation of authority logs
- Support close-out submissions and archival of trial documentation
- Ensure compliance with ICH, GCP, and FDA regulations
Required Qualifications
- Bachelor’s degree with 1 year of relevant experience in the life science industry OR
- Associate’s degree with 2 years of relevant experience in the life science industry OR
- High School Graduate and/or technical degree with a minimum of 3 years relevant experience in the life science industry
Required Skills
- Knowledge of medical terminology and regulatory documentation
- Understanding of ICH, GCP, and FDA regulatory requirements
- Strong written, verbal, and organizational skills
- Proficiency in Microsoft Office and office systems
- Ability to multitask and work independently
- Detail-oriented with strong professionalism
- Effective interpersonal and team collaboration skills
This role offers a solid foundation for professionals seeking structured Life Science Jobs in site-based clinical research. With direct involvement in regulatory compliance and study start-up activities, this opportunity under Velocity Careers is well-suited for candidates serious about building a stable and rewarding Clinical Research Career.
