You will get IRT RTSM - UAT Consulting Services
Project details
I am an Independent Clinical Monitor – HCP with a Pharma background and an MBA graduate, certified in Six Sigma, a Project Management Professional, ERP, and a self-starter (can work both collaboratively and independently)
Being a Healthcare expert with over 12 years of experience in pharmaceuticals /clinical research / CRO / monitoring clinical trials, mostly Oncology and Medical Device studies, seeks to use science background and record-breaking promotion strategies to build pharmaceuticals brand, awareness, and revenue.
I come with a handful of experience on RTSM, ICH-GCP, HIPAA, Quality Guidelines, SAP, CTMS Developing, CTMS, IRT/IWRS, EDC /EMR tools, Clinical Trial-Monitoring activities, Central Designing, Safety databases and monitoring, Clinical / MedDRA coding, Clinical Labelling, Pharmacovigilance and patient narrative, Patient Recruitment, Project Management, Project Planning, Project Coordination, Randomization, Enterprise Resource Planning, Site Management, SOP and Protocol review,
Being a Healthcare expert with over 12 years of experience in pharmaceuticals /clinical research / CRO / monitoring clinical trials, mostly Oncology and Medical Device studies, seeks to use science background and record-breaking promotion strategies to build pharmaceuticals brand, awareness, and revenue.
I come with a handful of experience on RTSM, ICH-GCP, HIPAA, Quality Guidelines, SAP, CTMS Developing, CTMS, IRT/IWRS, EDC /EMR tools, Clinical Trial-Monitoring activities, Central Designing, Safety databases and monitoring, Clinical / MedDRA coding, Clinical Labelling, Pharmacovigilance and patient narrative, Patient Recruitment, Project Management, Project Planning, Project Coordination, Randomization, Enterprise Resource Planning, Site Management, SOP and Protocol review,
Purpose
BusinessIndustry
Medical & PharmaceuticalLanguage
EnglishWhat's included
| Service Tiers |
Starter
$250
|
Standard
$500
|
Advanced
$1,000
|
|---|---|---|---|
| Delivery Time | 4 days | 5 days | 7 days |
Number of Revisions | 1 | 1 | 2 |
Number of Hours of Work | 32 | 40 | 60 |
Basic Photo Editing | - | - | - |
Organize & Classify/Tag Files | - | - | - |
Formatting & Clean Up | - | - | - |
Project Management Support | - | - | - |
Travel Planning | - | - | - |
Optional add-ons
You can add these on the next page.
Fast Delivery
+$300 - $1,500
30 reviews
(27)
(0)
(2)
(0)
(1)
This project doesn't have any reviews.
FG
Federico G.
Jul 16, 2025
Clinical trials data staffing and cost estimation
Malik is a great freelancer that helped us a lot with the clinical trial analysis for the investor
RS
Ram S.
May 22, 2023
Preparation of Informed Consent
The word done was full of mistakes, errors and typos.
MC
Merlynn C.
Oct 2, 2022
Looking for Clinical Project Manager
AS
Anushna S.
May 16, 2022
Clinical monitoring expert required to design overview of CRO requirements
Mallikarjun was very professional and always available during the project. His experience and skills are valuable and I would work with mallikarjun again in the future if the opportunity arises.
SV
Shweta V.
Dec 20, 2021
Clinical Trial Project - EDC developer
Its really good to work with him again and looking forward for more projects and work to be done with him.
About Mallikarjun
Clinical Research Prof/MBA - IRT(EDC/RTSM)-UAT Expert
Hyderabad, India - 12:14 am local time
Hope you are doing good.
I am Clinical Monitor – HCP (Registered Pharmacist) - with Pharma background and an MBA graduate, certified - Six Sigma, Project Management Professional, ERP and a self-starter (can work both collaboratively and independently).
Being a Healthcare expert with over 9.8 years of experience in pharmaceuticals /clinical research / CRO / monitoring clinical trials majorly Oncology studies,
I come with a handful experience on ICH-GCP, HIPAA, Quality Guidelines, SAP, CTMS Developing, EDC /EM(H)R / ePRO tools, Clinical Trial-Monitoring activities, Central Designing, Safety databases, Clinical / MedDRA coding , Pharmacovigilance and Patient narrative, Patient Recruitment, Project Management, Project Planning, Project Coordination, Randomization, Enterprise Resource Planning , Site Management, SOP and Protocol review. Have experience in Clinical Trial Management, eCRF designing, Live Study Programming abilities, Study Design, Six Sigma, eClinical Works, Citrix, Acumen, Medent, Pharmacovigilance, Adverse Event Reporting, Case Processing, Post Market Surveillance, Clinical Research, Medical Imaging, Supply Chain Management, Clinical Data Management, Stakeholders Management, and Pharmaceutical Marketing Management.
Steps for completing your project
After purchasing the project, send requirements so Mallikarjun can start the project.
Delivery time starts when Mallikarjun receives requirements from you.
Mallikarjun works on your project following the steps below.
Revisions may occur after the delivery date.
UAT Professional