You will get Statistical Data Analysis and Data cleaning with results
Top Rated
Top Rated
Project details
Client satisfaction is my ultimate goal and I strive to make you satisfied. I am flexible to all your requests. My Statistical Data Analysis and Data Cleaning Service stands out with my more than 8years experience proven by my publication indexed under SCOPUS and cited more than 100 times. I specialize in transforming raw, messy data into clear, actionable insights . I am accurate efficient using R, SPSS, NONMEM, etc
Whether you need help making sense of large datasets, building predictive models, or simply ensuring your data is clean and reliable, I am the right address
Whether you need help making sense of large datasets, building predictive models, or simply ensuring your data is clean and reliable, I am the right address
Data Tool
SPSSWhat's included
| Service Tiers |
Starter
$175
|
Standard
$300
|
Advanced
$500
|
|---|---|---|---|
| Delivery Time | 14 days | 20 days | 25 days |
Number of Revisions | 3 | 3 | 3 |
5 reviews
(5)
(0)
(0)
(0)
(0)
This project doesn't have any reviews.
ID
Irena D.
Oct 9, 2024
You will get Convert Masters/ PhD thesis/dissertation to publishable journal article
Very pleased, will work with her in the future.
Oh
Omar h.
Feb 22, 2024
Data analysis medical research , writing discussion, editing the whole paper
Thank you for your hard work and dedication on this project. Your ability to articulate complex ideas clearly and concisely is commendable.
Oh
Omar h.
Dec 30, 2023
intro and discussion edits
Excellent freelancer with a strong aptitude for academic writing and communication. Delivered high-quality work that was both clear and well-structured. Highly recommend for academic projects
Oh
Omar h.
Dec 23, 2023
Editing, writing, and until get published
DK
Diamantis K.
Dec 15, 2023
I need a writer to convert my thesis into a publishable paper
About Fatima Khalifa M. A.
Clinical Trials Specialist & Regulatory Submission
100%
Job Success
Istanbul, Turkey - 7:21 pm local time
My background focuses heavily on the new drug human trials framework, ensuring that complex clinical datasets, protocols, and study reports align seamlessly with FDA, EMA, and ICH-GCP expectations.
Core Areas of Regulatory & Operational Expertise:
= FDA & Global Regulatory Submission Readiness:
Comprehensive support in preparing, auditing, and reviewing critical regulatory documentation for Investigational New Drug (IND) applications and New Drug Application (NDA) packages. Expert in ensuring compliance across Common Technical Document (CTD/eCTD) modules, specifically Module 5 (Clinical Study Reports) and Module 2 (Clinical Summaries).
= Clinical Trial Data Governance:
Solid experience as a multi-site Clinical Research Associate (CRA), managing methodology compliance, auditing protocols across major health networks, and designing data pipelines that easily withstand stringent regulatory scrutiny.
= Pharmacometrics & Model-Informed Drug Development (MIDD), Model-Informed Precision Dosing (MIPD) Frameworks:
Highly proficient in translating complex datasets into predictive Model-Informed Drug Development (MIDD) and Model-Informed Precision Dosing (MIPD) workflows. Advanced expertise in population pharmacokinetic (PopPK) nonlinear mixed-effects modeling using NONMEM, PDx-Pop, and R data analytics
Why Premium Sponsors & CROs Hire Me:
= Award-Winning Clinical Track Record: Published author with 9 peer-reviewed articles in SCI-indexed journals and 2 book chapters. My clinical pharmacokinetic research has won 1st place honors at the American College of Clinical Pharmacy (ACCP) annual symposium and is actively cited within official international clinical guidelines (IDSA).
= Clinical Trials Alignment & Trilingual Communication: Operating as a Clinical Trials Specialist for overseas clinical studies, ensuring total familiarity with international operational speeds, timelines, and compliance standards. Trilingual proficiency in Arabic (native), English (C2), and Turkish (C1) allows me to coordinate seamlessly across multinational trial sites and global sponsor teams.
I treat regulatory compliance not just as an administrative task, but as a critical strategic milestone toward clinical success and market approval.
Let’s discuss how I can streamline your upcoming submission or audit your current trial data pipelines for maximum regulatory compliance. Click "Invite to Job" or "Message" to connect immediately.
My skills:
Regulatory Submissions
FDA Submissions
Regulatory Affairs
Clinical Trial Protocol
Clinical Research
GCP (Good Clinical Practice)
IND Applications
Pharmacokinetics
Pharmacodynamics
NONMEM
R
SPSS
STATA
Steps for completing your project
After purchasing the project, send requirements so Fatima Khalifa M. A. can start the project.
Delivery time starts when Fatima Khalifa M. A. receives requirements from you.
Fatima Khalifa M. A. works on your project following the steps below.
Revisions may occur after the delivery date.
Revise , clean the data, impute missing data if required, clean the data
Revise the data files, clean the data, impute missing data if required, clean the data
Determine statistical tests and graphics
Determine statistical tests and graphics are needed with the client and based on my suggestions per study objectives