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Sub Investigator | Clinical Trials & Patient Safety | Velocity Clinical Research

Velocity Clinical Research
Velocity Clinical Research
5+ years
Not Disclosed
10 March 26, 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

Sub Investigator | Clinical Trials & Patient Safety | Velocity Clinical Research

Company: Velocity Clinical Research
Job ID: 2026-3392
Job Type: Full-Time (Permanent)
Work Mode: On-site
Experience: 5+ Years
Location: Not explicitly specified (Clinical Research Site-Based Role)


Job Overview

Velocity Clinical Research is hiring a Sub Investigator to play a critical role in clinical trial execution, patient safety, and data integrity. This position supports Principal Investigators (PIs) and clinical teams in ensuring that studies are conducted in compliance with ICH-GCP, regulatory requirements, and protocol guidelines.

As a Sub Investigator, you will lead study activities, oversee patient care within trials, and ensure accurate clinical data collection, making this role central to the success of clinical research and drug development.


Key Responsibilities

Clinical Trial Execution & Oversight

  • Conduct and manage clinical trials in accordance with ICH-GCP, protocols, and SOPs

  • Lead study teams and ensure smooth execution of clinical research activities

  • Oversee study start-up, subject recruitment, conduct, and close-out

Patient Safety & Clinical Care

  • Ensure safety and well-being of all study participants

  • Evaluate subjects for trial eligibility (pre-screening and screening)

  • Perform clinical procedures such as drug administration, ECG, phlebotomy, lab processing

Data Management & Documentation

  • Ensure accurate and timely clinical data entry into EDC systems

  • Maintain Good Documentation Practices (GDP)

  • Resolve queries and ensure audit-ready documentation

Regulatory & Compliance

  • Prepare and submit documents to IRBs and sponsors

  • Ensure compliance with ICH-GCP, HIPAA, and regulatory standards

  • Manage protocol deviations, amendments, and reporting

Pharmacovigilance & Safety Reporting

  • Monitor and report Adverse Events (AE), Serious Adverse Events (SAE)

  • Ensure proper escalation and reporting as per protocol

Team Leadership & Training

  • Mentor and train clinical research staff and coordinators

  • Develop training strategies and quality control plans

  • Ensure staff delegation and training documentation

Project & Stakeholder Management

  • Coordinate with sponsors, CROs, vendors, and internal teams

  • Apply project management strategies to improve study quality and timelines

  • Develop recruitment strategies and operational plans


Required Skills & Qualifications

Educational Qualification

  • Licensed MD / DO / NP / PA (Mandatory)

Experience

  • Minimum 5+ years in clinical research / clinical trial management

Technical Skills

  • Strong knowledge of ICH-GCP, clinical trial protocols, and regulatory requirements

  • Experience with clinical trial operations, EDC systems, and regulatory submissions

  • Understanding of pharmacovigilance and safety reporting (AE/SAE)

  • Familiarity with HIPAA compliance and patient data protection

Core Competencies

  • Strong leadership and team management skills

  • Excellent communication and stakeholder coordination

  • High attention to detail and compliance-driven mindset

  • Ability to manage multiple trials and priorities

  • Strong problem-solving and decision-making ability


Perks & Benefits

  • Comprehensive medical, dental, and vision insurance

  • Paid time off and company holidays

  • 401(k) retirement plan with company match

  • Annual performance-based incentive program

  • Career growth opportunities in clinical research and drug development

  • Work in a patient-centric, high-impact clinical environment


Compensation

  • Salary Range: Not disclosed (competitive based on experience and clinical research standards)


About the Company

Velocity Clinical Research is a leading integrated clinical research site organization focused on high-quality data generation, patient care, and efficient clinical trial execution. The company partners with sponsors and CROs to accelerate drug development and bring innovative treatments to patients globally.


Why This Role is High-Impact

This role is ideal for professionals aiming to grow in:

  • Clinical Research & Trial Leadership

  • Patient Safety & Clinical Care in Trials

  • Pharmacovigilance & Drug Safety

  • Regulatory Affairs & Compliance

  • Drug Development Lifecycle


Application Process

Apply via the official Velocity Clinical Research careers portal.


Call to Action

If you want to be at the core of clinical trials—ensuring patient safety while advancing new treatments—this is your opportunity.

Step into a role where medicine meets research, and patient care drives innovation.
Apply now and become a key player in clinical development. 🚀