www.phoenixclinicalresearch.com Phoenix Clinical Research Pvt Ltd Jaipur : Clinical Research Coordinator

[STSRekha]

Company Name : Phoenix Clinical Research Pvt Ltd
Company Location : Jaipur
Designation : Clinical Research Coordinator

Contact us :
Phoenix Clinical Research Pvt Ltd
B-105, Sethi Colony,
Agra Road
Jaipur-302004,
Rajasthan, India

About us :
Phoenix Clinical Research is an India based Contract Research Organization (CRO). We offer Clinical Trials Services in India to pharmaceutical, biotechnology, and medical device companies. We provide our clients with an offshore cost advantage combined with faster patient recruitment and quality data.
We offer all services from phase I through phase IV clinical trials and BA/BE studies.

Clinical Research Associates :
Qualification : MBBS, B.Pharma, M.Pharma, BDS

Clinical Research Coordinator :
Qualification : Science Graduates, MBBS, B.Pharma, M.Pharma, BDS

How to Apply :
Mail resumes to contact@phoenixclinicalresearch.com

Web : http://www.phoenixclinicalresearch.com

General Instructions :
1) This is a job in Phoenix Clinical Research Pvt Ltd at Jaipur for the post of Clinical Research Coordinator.
2) For more details refer to the company website.
3) You can send resume / CV to the company's email address.
4) Source of the information is the company website / internet on the date of publishing.

[Guest]

DEEPAK SANGWAN
E-mail : dpksangwan AT yahoo.co.in
dpksangwan AT gmail.com
SUMMARY
I am a Post Graduate in Biotechnology. My aim is to carve out a niche for myself marked by professional excellence while actively contributing to the development of the organization employing my skills.
PROFESSIONAL EXPERIENCE
SRL Religare Gurgaon, India 2008 Summer Intern
(Formally SRL Ranbaxy Ltd)
Did a project on LIPID ELECTROPHORESIS (using LIPOPRINT, SERUM PROTEIN ELECTROPHORESIS (using HYDRASYS) & ANALYTE STABILITY (using DADE DIMENSION RxL)
ALCHEM INTERNATIONAL LTD Faridabad, India 2009
Did a 3 month training in fermentation technology and Down Stream Processing (DSP)
Fortis Clinical Research Faridabad, India 2009
Worked as a on Job Trainee in the Quality Assurance unit of FCRL.
Fortis Clinical Research Faridabad, India 2009- Present
Currently working as a QC Executive in the Quality Control Department of FCRL.
Key Responsibilities :
1 Preparation of Protocol, Informed consent document, Case Record Forms and other related documents as per the applicable regulatory guidelines (USFDA, EMEA, ANVISA, DCGI).
2 Reviewing of TMF, Raw data, CRF’s and other trial related documents during the study and retrospectively.
3 Assisting in the preparation and review of Clinical Study Report as per the ICH E3/ANVISA guidelines.
4 QC check of case narratives of Adverse Events and Serious Adverse events.
5 Final diagnosis of Adverse Events in clinical study report as per the MedDRA.
6 Preparation of monitoring reports.
7 Assisting the team in the preparation of Standard Operating Procedures.
8 Providing training on various Standard Operating Procedure’s to the study personnel’s.
9 Assisting the team for the preparation of audits and inspections.
10 Managing and coordinating with team to maintain Sponsor timelines.
11 Review of eCTD before its submission to Sponsor.
OTHER HIGHLIGHTS
- Deep knowledge of monitoring procedures.
- Detailed knowledge of GCP and ICH guidelines including basic understanding of regulatory requirements.
- Basic knowledge of clinical trial process.
- Successfully assisted the team in the conduction of two FDA inspections.
- Enthusiastic, Eager and Work effectively independently or as a part of a team.
- Webinar attended on topics like :
- Coding as per MedDRA
- Clinical trial Chain Supply Management
EDUCATION
Advance PG Program in CLINICAL RESEARCH 2009
(Cliniminds, New Delhi)
AMITY University, MSc Biotechnology 2007-2009
INDRAPRASTHA ENGINEERING COLLEGE 2004-2007
CCS University
BSc. in Biotechnology
KENDRIYA VIDYALAYA No.3 2004
Class XII from CBSE Board
KENDRIYA VIDYALAYA No.3 2002
Class X from CBSE Board
STRENGTH
1 Team player and can work with same efficiency as a individual
2 Fast learner
3 Good at time management
4 Positive attitude
5 Keen observer
6 Ready and willing to accommodate frequent local, domestic or international business travel
COMPUTER PROFICENCY
1 Working knowledge of MS Word, Power Point, Excel and Internet.

[Guest]

Subject : Regarding Idustrial Project in Pharmacological field.

Respected Sir,

My self Atul kabra, I've done B.pharma from Pacific college of pharmacy,Udaipur & currently pursuing M.Pharma in Pharmacology from G.H.B. pharmacy college .
This is regarding project in your organisation, please allow me for Industrial Project.

All the details are available in my resume. please find the attachement.

CURRICULUM VITAE
ATUL KABRA
E-mail : atul.kbr AT gmail.com

Objective
To excel professionally, gaining hands on experience in a growth oriented organization where I can enhance my knowledge base.
Qualifications
- Academic Qualification
M.Pharma First semester (65%) & Second semester result is awaited.
First class (69.69%) B.pharma from Pacific college of pharmacy, Udaipur ((Rajasthan)
Passed Higher Secondary Certificate (H.S.C.) from Rajasthan Board with a First Class (60%) in the year 2005.
Passed Senior Secondary Certificate (S.S.C.) from Rajasthan Board Education (R.B.S.E.) with a First Class (62%) in the year 2003
Project Undertaken(B. PHARMA)
Project – Bioavailabilitiy & Bioequilence
Honors & Awards
School Awards
Poetry Competition award 1997
Gandhi Quiz award 2001
College Awards
Poster presentation award 2009
Essay competition award 2010
Achievement
GPAT qualify in 2010