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Protocol Process Deviation Reporting

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MV

Meera Vyas@meeravyas

Pharmacovigilance Specialist Clinical Research Coordinator Pharmacovigilance Clinical Research

Clinical Research and Pharmacovigilance professional dedicated to patient safety.

Experience

TB

Tapas Kumar Bishoyi@tapaskumarbishoyi

Quality Systems Director GMP Quality GMP Compliance Quality Systems

Senior GMP compliance and quality systems leader building audit-ready, data-integrity-first operations in regulated API pharma.

RM

Ranjith Munukuntla@ranjithmunukuntla

1800k-2450k USD

Quality Assurance Specialist Quality Assurance GxP

MS

Makayla Smart@makaylasmart

Quality Assurance Quality Assurance Auditing GMP Documentation Deviation Management

I’m a Senior Quality Assurance professional driving GMP deviations to actionable CAPAs, continuous improvement, and audit-ready compliance.

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PE

Pamela Egan@pamelaegan

Quality Assurance Manager Regulatory Affairs Specialist Compliance Regulatory Strategy

Experienced Quality Assurance professional with extensive regulatory expertise.

Experience

AR

Albert Roberson@albertroberson

Process Engineer Quality And Safety Systems Manager Supplier Quality Audits Mock Audits

I am a GMP-trained process engineer with 8+ years in API manufacturing and quality systems.

Experience

RP

Rishitha P@rishithap

Clinical Research Coordinator Health Information Analyst Phase I Phase II

Clinical Research Coordinator with 5+ years managing Phase I–IV trials, ensuring GCP compliance, safety, and high-quality data.

AR

Aisha Robinson@aisharobinson

Compliance Manager Quality Assurance Specialist GMP CGMP Requirements

Quality and operations specialist delivering compliant GMP readiness through training consistently.

Experience

MS

Melissa Schulz@melissaschulz

Quality Assurance & Compliance Quality Assurance Management SOP Lifecycle Management

Quality & compliance operations leader improving regulated reliability and audit readiness.

Experience

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BA

Bukola Amos@bukolaamos

Clinical Research Associate Clinical Operations Clinical Monitoring Site Oversight

Senior Clinical Research Associate with 9+ years managing global oncology and complex-indication trials.

Experience

SN

Swarali Nikam@swaralinikam

Clinical Quality Assurance GxP Auditing Quality Management Systems SOP Development

Clinical Quality Assurance leader with 13+ years in GxP audits, QMS, and inspection readiness.

Experience

MO

Michelle Orlere@michelleorlere

Clinical Research Associate II In House CRA Remote Veeva Vault ETMF

Clinical Research Associate with 8+ years leading risk-based monitoring and audit-ready eTMF oversight across global Phase I–III trials.

FN

Farha naaz@farhanaaz1

Healthcare Documentation Reviewer Clinical Data Management Clinical Trial Coordination Patient Recruitment

Clinical Research Coordinator with 3+ years managing Phase III trials, ensuring ICH-GCP compliance, data integrity, and audit-ready sites.

AS

Apar Sharma@aparsharma

Computer System Validation (CSV)Validation Specialist Sciex Analyst IQ Tests

Computer System Validation specialist focused on GAMP 5, 21 CFR Part 11, and ALCOA+ data integrity.

Experience

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US

Urvi Sadariya@urvisadariya

Medical Writer Drug Safety Management Remote Pharmacovigilance

Detail-oriented pharmacovigilance professional skilled in case processing, medical writing, and regulatory-compliant drug safety operations.

Experience

AC

Alexandria Childs@alexandriachilds

Quality Management Specialist Quality Assurance Batch Record Review CAPA

Quality-focused microbiology scientist skilled in GMP documentation and inspection readiness.

HA

Henry Arevalo@henryarevalo

Quality Assurance Manager Production Control Supervisor Quality Assurance Validation

Senior Quality Assurance professional with expertise in pharmaceutical validation.

Experience

DV

Daniel VH@danielvh

Quality Assurance Specialist Quality Auditor Quality Assurance Quality Management Systems

Quality assurance specialist driving compliance, audits, and continuous improvement.

KJ

Kashish Jain@kashishjain1

Regulatory Affairs Specialist Regulatory Affairs Associate Regulatory Strategy Regulatory Submissions

Detail-oriented quality professional with experience in QA/QC, documentation, audits, and compliance. Remote-ready and highly organized.

BY

Brian Yun@brianyun

Clinical Operations Manager Quality Systems Clinical Operations Quality Systems

I lead clinical operations and quality systems, driving regulatory compliance and LIS strategy for multi-site throughput.