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Specialist Ii, Regulatory

Velocity Clinical Research
Velocity Clinical Research
2-6 years
Not Disclosed
10 March 19, 2026
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Specialist II, Regulatory

Company: Velocity Clinical Research
Location: On-site
Job Type: Full-Time
Experience: 2–6 Years (depending on qualification)
Qualification: Bachelor’s / Associate Degree / Equivalent Experience


Job Overview

This role focuses on regulatory document preparation, submission, and maintenance for clinical research studies. You will ensure compliance with IRB, FDA, and ICH-GCP requirements while supporting study start-up, execution, and close-out activities.


Key Responsibilities

Regulatory Submissions & Documentation

  • Prepare and submit study protocols, ICFs, HIPAA forms, and IRB documents

  • Handle amendments, continuing reviews, adverse event reports, and deviations

  • Ensure timely submissions to avoid delays in study start-up

Compliance & Regulatory Management

  • Maintain regulatory binders (paper/electronic) for audit readiness

  • Ensure compliance with ICH-GCP and FDA guidelines

  • Stay updated with regulatory changes and implement accordingly

Study Support & Coordination

  • Support study start-up and regulatory readiness activities

  • Assist in financial disclosure documentation

  • Coordinate with sponsors, IRBs, and internal teams

Training & Team Support

  • Track staff training records and expiration timelines

  • Assist new hires with documentation and compliance training

  • Support delegation of authority logs and staff documentation

Audit & Inspection Readiness

  • Prepare for monitoring visits, sponsor audits, and regulatory inspections

  • Conduct quality checks of regulatory files

  • Coordinate audit meetings and documentation review

Study Close-Out

  • Prepare and submit close-out documents to IRB and sponsors

  • Ensure proper archiving of regulatory files


Required Skills

Knowledge of ICH-GCP and FDA regulations

Regulatory documentation and submission experience

Attention to detail and organizational skills

Communication and coordination abilities

Ability to multitask in a fast-paced environment


Preferred Skills

Clinical research certification (CCRP or equivalent)

Experience mentoring or leading junior staff

Strong problem-solving and leadership skills