Revathi Sriram Email & Phone Number
Who is Revathi Sriram? Overview
A concise factual answer block for searchers comparing this professional profile.
Revathi Sriram is listed as Clinical Research Associate III | Clinical Data Analyst | Data Analyst | Clinical Trails | Clinical Trail Management Systems | Clinical Data Management | Clinical Data Analysis at Advarra, a with 302 employees, based in Tirupati Urban, Andhra Pradesh, India. AeroLeads shows a matched LinkedIn profile for Revathi Sriram.
Revathi Sriram previously worked as Research Associate III at Advarra and Research Associate III at Advarra. Revathi Sriram holds Bachelor Of Pharmacy - Bpharm, Pharmacy, First Class With Distinction from Sri Padmavathi School Of Pharmacy, Tirupathi.
Email format at Advarra
This section adds company-level context without repeating Revathi Sriram's masked contact details.
Review company-level records connected to Revathi Sriram before choosing the right outreach path.
About Revathi Sriram
Healthcare Professional with a Bachelor's degree in Pharmacy, and Google Data Analytics Professional Certificate with an overall experience of 3 years in clinical research domain involving clinical trail protocol interpretation, study schedule set up, clinical trail study budget (grants) analysis, US Medicare coverage analysis during the study start up phase in clinical trail management system (CTMS) - Oncore.My expertise includes handling clinical trail management system (CTMS) - Oncore, Advarra EDC software, clinical data management (CDM), Clinical Trail Study Budget (Grants) Analysis, US Medicare Coverage Analysis, Protocol Design, Good clinical Practice, ICH guidelines. Dealt with study start up phases of various clinical trails with wide range of therapeutic indications including both oncology and non oncology. Expertise in clinical data curation and data review from Pub med, Medicare, clinicaltrails.gov, other clinical trail registries etc., Highly motivated, committed and disciplined team player with a flexible approach to work and take initiative whenever possible. Good interpersonal skills and learning attitude to adapt to changing work environment.
Revathi Sriram's current company
Company context helps verify the profile and gives searchers a useful next step.
Revathi Sriram work experience
A career timeline built from the work history available for this profile.
Research Associate Iii
* Responsible for performing Medicare coverage analysis for clinical trails (oncology, non-oncology and device studies) utilizing clinical study protocols, sponsor budgets, clinical trail agreements (CTA) along with data curated and reviewed from NCCN Guidelines, PubMed, Medicare.gov, clinical trail registries and other registries etc., * Responsible for creating calendars/ study visits for clinical studies utilizing clinical study protocols.* Responsible for setting up of study… Show more * Responsible for performing Medicare coverage analysis for clinical trails (oncology, non-oncology and device studies) utilizing clinical study protocols, sponsor budgets, clinical trail agreements (CTA) along with data curated and reviewed from NCCN Guidelines, PubMed, Medicare.gov, clinical trail registries and other registries etc., * Responsible for creating calendars/ study visits for clinical studies utilizing clinical study protocols.* Responsible for setting up of study budgets/ grants for clinical trails utilizing clinical study protocols, sponsor budgets and clinical trail agreements (CTA).* Expertise in theoretical knowledge of multiple clinical Indications - oncology, cardiology, neurology, nephrology, metabolic and neuro-degenerative disorders etc.,* Responsible for designing and developing case report forms (crf's) for clinical trial study protocols * Collaborated with clinical study sites and sponsors to troubleshoot and provide solutions to study-related issues * Collaborated with clinical sites using clinical trial management system (CTMS) and electronic data capture (EDC) software to utilize related functionalities in the design and development of calendars, budgets, and case report forms during study start up phase.* Mentored team members to deliver successful studies. Show less
Research Associate Ii
* Responsible for performing Medicare coverage analysis for clinical trails (oncology, non-oncology and device studies) utilizing clinical study protocols, sponsor budgets, clinical trail agreements (CTA) along with data curated and reviewed from NCCN Guidelines, PubMed, Medicare.gov, clinical trail registries and other registries etc., * Responsible for creating calendars/ study visits for clinical studies utilizing clinical study protocols.* Responsible for setting up of study… Show more * Responsible for performing Medicare coverage analysis for clinical trails (oncology, non-oncology and device studies) utilizing clinical study protocols, sponsor budgets, clinical trail agreements (CTA) along with data curated and reviewed from NCCN Guidelines, PubMed, Medicare.gov, clinical trail registries and other registries etc., * Responsible for creating calendars/ study visits for clinical studies utilizing clinical study protocols.* Responsible for setting up of study budgets/ grants for clinical trails utilizing clinical study protocols, sponsor budgets and clinical trail agreements (CTA).* Expertise in theoretical knowledge of multiple clinical Indications - oncology, cardiology, neurology, nephrology, metabolic and neuro-degenerative disorders etc.,* Responsible for designing and developing case report forms (crf's) for clinical trial study protocols * Collaborated with clinical study sites and sponsors to troubleshoot and provide solutions to study-related issues * Collaborated with clinical sites using clinical trial management system (CTMS) and electronic data capture (EDC) software to utilize related functionalities in the design and development of calendars, budgets, and case report forms during study start up phase.* Mentored team members to deliver successful studies. Show less
Research Associate I
* Responsible for performing Medicare coverage analysis for clinical trails (oncology, non-oncology and device studies) utilizing clinical study protocols, sponsor budgets, clinical trail agreements (CTA) along with data curated and reviewed from NCCN Guidelines, PubMed, Medicare.gov, clinical trail registries and other registries etc., * Responsible for creating calendars/ study visits for clinical studies utilizing clinical study protocols.* Responsible for setting up of study… Show more * Responsible for performing Medicare coverage analysis for clinical trails (oncology, non-oncology and device studies) utilizing clinical study protocols, sponsor budgets, clinical trail agreements (CTA) along with data curated and reviewed from NCCN Guidelines, PubMed, Medicare.gov, clinical trail registries and other registries etc., * Responsible for creating calendars/ study visits for clinical studies utilizing clinical study protocols.* Responsible for setting up of study budgets/ grants for clinical trails utilizing clinical study protocols, sponsor budgets and clinical trail agreements (CTA).* Expertise in theoretical knowledge of multiple clinical Indications - oncology, cardiology, neurology, nephrology, metabolic and neuro-degenerative disorders etc.,* Responsible for designing and developing case report forms (crf's) for clinical trial study protocols * Collaborated with clinical study sites and sponsors to troubleshoot and provide solutions to study-related issues * Collaborated with clinical sites using clinical trial management system (CTMS) and electronic data capture (EDC) software to utilize related functionalities in the design and development of calendars, budgets, and case report forms during study start up phase Show less
Research Associate Intern
* Responsible for creating calendars/ study visits for clinical studies utilizing clinical study protocols.* Responsible for setting up of study budgets/ grants for clinical trails utilizing clinical study protocols, sponsor budgets and clinical trail agreements (CTA).* Expertise in theoretical knowledge of multiple clinical Indications - oncology, cardiology, neurology, nephrology, metabolic and neuro-degenerative disorders etc.,* Responsible for designing and developing case… Show more * Responsible for creating calendars/ study visits for clinical studies utilizing clinical study protocols.* Responsible for setting up of study budgets/ grants for clinical trails utilizing clinical study protocols, sponsor budgets and clinical trail agreements (CTA).* Expertise in theoretical knowledge of multiple clinical Indications - oncology, cardiology, neurology, nephrology, metabolic and neuro-degenerative disorders etc.,* Responsible for designing and developing case report forms (crf's) for clinical trial study protocols * Collaborated with clinical study sites and sponsors to troubleshoot and provide solutions to study-related issues * Collaborated with clinical sites using clinical trial management system (CTMS) and electronic data capture (EDC) software to utilize related functionalities in the design and development of calendars, budgets, and case report forms during study start up phase. Show less
Colleagues at Advarra
Other employees you can reach at advarra.com. View company contacts for 302 employees →
Shari Somerstein
Colleague at AdvarraFort Lauderdale, Florida, United States
View →
AH
Annie Hoang
Colleague at AdvarraStevensville, Maryland, United States
View →
ST
Sruthy T S
Colleague at AdvarraMalappuram, Kerala, India
View →
AC
Alyssa Carter
Colleague at AdvarraHuntsville-Decatur-Albertville Area, United States
View →
MM
Maria Mccormack
Colleague at AdvarraIreland
View →
MW
Mark Wolski
Colleague at AdvarraGlendale, Arizona, United States
View →
TP
Thao P Sweeny
Colleague at AdvarraChula Vista, California, United States
View →
JW
John Weisenreider
Colleague at AdvarraWinnabow, North Carolina, United States
View →
DS
Dr. Sandeep K G
Colleague at AdvarraChennai, Tamil Nadu, India
View →
RI
Ramakant Irrangi
Colleague at AdvarraBangalore Urban, Karnataka, India
View →
Revathi Sriram education
-
Sri Padmavathi School Of Pharmacy, Tirupathi
Frequently asked questions about Revathi Sriram
Quick answers generated from the profile data available on this page.
What company does Revathi Sriram work for?
Revathi Sriram works for Advarra.
What is Revathi Sriram's role at Advarra?
Revathi Sriram is listed as Clinical Research Associate III | Clinical Data Analyst | Data Analyst | Clinical Trails | Clinical Trail Management Systems | Clinical Data Management | Clinical Data Analysis at Advarra.
Where is Revathi Sriram based?
Revathi Sriram is based in Tirupati Urban, Andhra Pradesh, India while working with Advarra.
What companies has Revathi Sriram worked for?
Revathi Sriram has worked for Advarra.
Who are Revathi Sriram's colleagues at Advarra?
Revathi Sriram's colleagues at Advarra include Shari Somerstein, Annie Hoang, Sruthy T S, Alyssa Carter, and Maria Mccormack.
How can I contact Revathi Sriram?
You can use AeroLeads to view verified contact signals for Revathi Sriram at Advarra, including work email, phone, and LinkedIn data when available.
What schools did Revathi Sriram attend?
Revathi Sriram holds Bachelor Of Pharmacy - Bpharm, Pharmacy, First Class With Distinction from Sri Padmavathi School Of Pharmacy, Tirupathi.
Search by job title, company, industry, location, and seniority. Export verified B2B contact data when you need it.
Start free trialCheck these profiles if this is not the Revathi Sriram you were looking for.
View similar profiles