You will get Clinical Trial Support for Oncology and Pharma Studies
Project details
I am a PharmD and MSc in Cancer & Clinical Oncology graduate with hands-on experience in clinical research, oncology-focused studies, and scientific medical writing. I specialize in supporting pharmaceutical companies, CROs, and research teams with high-quality clinical trial documentation, protocol review, literature reviews, regulatory writing, and evidence synthesis.
With practical exposure to ICH-GCP–compliant research environments and cross-functional collaboration with clinicians, data managers, and investigators, I ensure that every deliverable is accurate, compliant, and aligned with global clinical standards.
My work focuses on transforming complex clinical and scientific data into clear, structured, and publication-ready documentation that supports efficient decision-making and research progression.
I am committed to delivering precision, reliability, and clarity across all stages of clinical development, helping clients save time, reduce workload, and maintain the highest quality standards in their research outputs.
With practical exposure to ICH-GCP–compliant research environments and cross-functional collaboration with clinicians, data managers, and investigators, I ensure that every deliverable is accurate, compliant, and aligned with global clinical standards.
My work focuses on transforming complex clinical and scientific data into clear, structured, and publication-ready documentation that supports efficient decision-making and research progression.
I am committed to delivering precision, reliability, and clarity across all stages of clinical development, helping clients save time, reduce workload, and maintain the highest quality standards in their research outputs.
Target Country
Worldwide, United States, United KingdomWhat's included
| Service Tiers |
Starter
$30
|
Standard
$45
|
Advanced
$79
|
|---|---|---|---|
| Delivery Time | 3 days | 2 days | 2 days |
Number of Projects | 2 | ||
General Project Consulting | |||
Define Project Goals | |||
Define Deliverables & KPIs | - | ||
Establish Schedule & Milestones | |||
Risk Management | - | ||
Resource Management | - | ||
Budget Management | - | - | |
Project Reports | - | ||
Project Diagrams Provided | - | - |
Optional add-ons
You can add these on the next page.
Fast Delivery
+$15 - $25
Additional Project
(+ 5 Days)
+$25
Define Deliverables & KPIs
+$30
Risk Management
+$28
Resource Management
+$50
Budget Management
+$50
Project Reports Provided
+$50
Project Diagrams Provided
+$100About Meghana
Virtual Assistance | Pharmacology, Clinical Trial, Medicine
London, United Kingdom - 3:49 am local time
Clinically trained Pharm.D + MSc in Cancer & Clinical Oncology (Distinction) with strong expertise in clinical research, oncology, hematology, and medical writing.
I provide clinical trial operations support, oncology trial consulting, protocol review, literature reviews, regulatory documentation, and trial feasibility assessments. Experienced in working within ICH-GCP–compliant environments and cross-functional research teams across academia and industry (pharma+ Medical device).
Skilled in translating complex clinical and scientific data into clear, compliant, and evidence-based documentation to support medical affairs, R&D, and clinical development.
📍 Based in London, UK | Open to remote collaboration
💼 Services from £25/hour
Steps for completing your project
After purchasing the project, send requirements so Meghana can start the project.
Delivery time starts when Meghana receives requirements from you.
Meghana works on your project following the steps below.
Revisions may occur after the delivery date.
Client purchases the project and sends requirements.