Mrs. Preeti Sirohi

Email : Preetidahiya006@gmail.com

Contact: +61-450668868

Visa status: Full time working visa, Class UF(Subclass 309) partner provisional (Australia)

Address: 3/64 Pine street, Reservoir VIC (Melbourne)-3073

Experienced ICH-GCP certified, hand on Oracle clinical ,worked in Hospitals as Clinical research coordinator over 2 years of experience, looking for new opportunities within Clinical Research , currently working as volunteer with Sunshine school with specially able children.

1. Organization : CRC at JSS Medical (Former Max Neeman International)

Duration : Mar 2015 - Jul 2016

Role : Clinical Research Coordinator

Project Undertaken: Phase IV studies, Gastroenterologist-Peptic Ulcer, Oncology, neurology and Observational studies.

Key Role and Responsibilities :

Under gone study specific trainings, provide ICH-GCP training to the investigators

Worked with Oracle clinical ,e-CRF entry ,IVRS system

Get Study related documents Signed from all the Investigators

Screen Subjects with inclusion/exclusion criteria and register to site (maintain confidentiality)

EC submissions and attending EC meetings

Make subjects understand the protocol, CRF with layman language

Schedule patient visits, track on lab sample collection, write source notes including subject data, IP accountability, register IVRS, update CRFs and documents signed by PI

Maintains study files in accordance with sponsor requirements, maintain IP storage temperature, funding to subjects, resolve various queries of subjects over phone and time to time follow up.

Description:

2. Organization: Apollo Hospitals Educational and Research Foundation (AHERF)

Duration: Aug 2013 - Sept 2014.

Role: Trainee Clinical Research Coordinator

Key Role and Responsibilities :

All work done under the guidance of site CRC as a co-worker which includes:

Helping study subjects to fill new versions of ICF.

Resolving patient queries over phone and make them to understand study protocol in layman language.

Maintain IP storage temperature as per protocol.

Schedule patient visits and take track on patient lab samples in site central Lab.

Attend monitoring visits and helping in resolving queries including proper filing and arranging as per proposed index.

keep a track on Patient visits.

Course , Institute (University or Board) Duration

Advanced Certificate course in clinical research (Apollo Hospital) Delhi Sept. 2013-Mar 2014

M.Sc Bioinformatics (MDU INDIA) 2012-2013

Bachelor of education (MDU Rohtak) 2009-2010

Diploma in bioinformatics (Zamia Hamdard University, New Delhi) 2008-2009

BSc. Life science (MDU Rohtak) 2005-2008

Passed year 12 (CBSE) 2004-2005

Passed year 10 (HBSE) 2002-2003

Academics :

Projects:

1. Course : ACCR clinical research course Apollo Hospital New Delhi

Project : Conducted corporate survey "To Derive The Most Efficient Software Used In Clinical Data Management".

(Project report submitted for partial fulfillment of requirement for the award of ACCR at Apollo Hospitals, New Delhi).

2. Degree : Masters in Bioinformatics

Duration : 2012- 2013

Thesis Project: study target site of drug interaction factor IX blood coagulation using YASARA software (6 Months).

3. Prepared protocol for " Superiority Assessment of Fenoterol over Salbutamol."

4. Review of literature and data extraction.

5. Prepared CRF for " Protocol title: A randomized, double blind, parallel phase III superiority study to prove superiority of Drug F over Drug S in patients with mild chronic bronchial asthma (age group 23-75 yrs)."

“Sensitization workshop on research methods” held at “National Institute of Epidemiology’’ Chennai.

“Workshop on GCP ”as part of Clinical Research Course.

Handled Phase IV Gastroenterologist-Peptic Ulcer survey as TL alone.

Knowledge of CDM software: OpenClinica, Argus, oracle clinical.

Knowledge of PV software: ARISg.

Training on ICF, CRF, SOP, PSURs, DSURs.

Computer Skill :- MS-Office, Mail Outlook.

Softwares & Tools used :- SMART , MSA, YASARA Mustang (Homology modeling), phylogenetic analysis, EXPASY.

Basic Knowledge of other aspects of Clinical research as ICH/GCP guidelines and historical background.

Workshops Attended:

Core Competencies:

Awards and Accomplishments:

"Max Neeman Star Award "July 2014,Issuer: Chief Operating Officer Max Neman International (JSS medical research).

"Life Achievement Award" 2015.

GCP certified by Medanta Institute of Education and Research.

Participated in 26 Jan 2004 Independence day PARADE (Ministry of Defense) in Class XI.

Participated in co-curricular activities and competitions in youth fest 2011-2013.

Clinical Trial Operation

Clinical Data Management

Regulatory/Ethics Committee

Pharmacovigilance

BA/BE Studies.

Area of Interest: