www.ayushsoftware.com Ayush Software Pvt Ltd Pune : Social Media Marketer

[muthukalee]

Social Media Marketer
We are looking for a person who has at-least one year experience in marketing a website through social media.

Experience: 1 year.

Education: Graduate from any stream

Job Location: Bhavdhan Office, Pune

Skills: A good knowledge on how social media networks works and how a website can be marketed through it.

To apply for any of the above jobs, send your resume to jobs@ayushsoftware.com. Please do mention the job position in your email for which you are making the application for.

About us :
Ayush Software is an Internet Web Solutions provider company based in the city of Pune, India. We are currently a small company but expanding vary fast.We mainly specialize into three fields, creating quality website content, SEO (search engine optimization) & SEM (search engine marketing), and website management.We have a team of highly skilled content writers, search engine optimizers, web designers, web developers and programmers. We are expanding exponentially.

Contact us :
Ayush Software Pvt. Ltd.
I-Space, Mumbai-Bangalore Highway,
Bhavdhan, Pune
Maharashtra, 411021, India
Phone Number(s) :
+91-20-42126000 (30 lines)
http://www.ayushsoftware.com

[Guest-IJT]

Name : Indira Nuthakki
Email : inuthakki AT gmail.com
Designation / Skillset : Medical Writer/Scientific Content Writer
Grow to an optimum level in the field of clinical research by efficiently making use of the knowledge that I have acquired through my Graduate and Post-graduate degrees in Chemistry and Pharmacology respectively. I have already gained experience working for 2 years as a Pharmacovigilance Associate and Medical Writer for Reliance Clinical Research Services for a period of 1 year followed by a period of 1.8 years at Tata Consultancy Services as a Process Executive in the Drug Safety Department for an ongoing clinical trial. I would further like to enhance my knowledge and establish myself in the field of Medical writing. I aim towards making medical writing simple and succinct through my words so that even a person from a non-scientific background can understand science without much struggle.

Resume :

OBJECTIVE :
Grow to an optimum level in the field of clinical research by efficiently making use of the knowledge that I have acquired through my Graduate and Post-graduate degrees in Chemistry and Pharmacology respectively. I have already gained experience working for 2 years as a Pharmacovigilance Associate and Medical Writer for Reliance Clinical Research Services for a period of 1 year followed by a period of 1.8 years at Tata Consultancy Services as a Process Executive in the Drug Safety Department for an ongoing clinical trial. I would further like to enhance my knowledge and establish myself in the field of Medical writing. I aim towards making medical writing simple and succinct through my words so that even a person from a non-scientific background can understand science without much struggle.
PERSONAL PROFILE :
Over the years I have acquired proficiency in drug action, drug metabolism, and all aspects of Pharmacology, Pharmacovigilance, Feasibility, Early Development; Study Details and Medical Writing. In addition to this, my Master’s project which involved testing the effect of a novel drug NED-14 that was known to inhibit calcium release from the Nicotinic Acid Adenine Dinucleotide Phosphate (NAADP) receptor in the development of a lysosomal storage disorder also introduced me to the underlying principles of Molecular Biology. Through the MSc course I was able to write scientific essays on a wide range of topics and have also given several oral and poster presentations. I returned to my home country to make best possible use of the knowledge that I had gained and joined the Medical Affairs Department at Reliance Clinical Research Services as a Trainee. Here I was privileged enough to learn all the medical aspects of clinical research. Initially I underwent intensive training in Pharmacovigilance (SAE Reporting) and within a span of 4 months I was promoted to the post of a Pharmacovigilance Associate; I was also involved in Feasibility studies. Additionally, I was also trained in all aspects of Bioequivalence and Bioavailability studies and have also written protocols for bioequivalence studies. Even though I was enlightened with a plethora of knowledge my experiences have made me realize that in this field there is still so much to discover and learn and that makes it all the more fascinating, armed with these experiences and my expertise I would like to establish myself in the field of Medical Writing.
EDUCATIONAL QUALIFICATIONS :
2006-2007 : MSc in Pharmacology, University of Oxford
- Experience in in vitro and organ bath pharmacology, Molecular pharmacology,
- Basic cell biology techniques (tissue culture) and in vivo whole system pharmacology.
2003-2006 : BSc in Chemistry (First Class), St. Xavier’s College, Mumbai University
Modules :
1) Physical Chemistry
2) Analytical Chemistry
3) Organic Chemistry
4) Inorganic Chemistry
5) Drugs
6) Dyes
2000-2002 : Higher Secondary School Certificate
- First Class with a distinction in Science
1999-2000 : National (India) Senior Secondary School Examinations, Gopi Birla Memorial High School
- First Class with distinction
___________________________________________________________________________
RESEARCH AND QUALIFICATIONS.
2007 : Scientific Writing Skills Workshop, (Department of Pharmacology, University of Oxford).
2007 : Investigating the role of NED-14: A potential NAADP receptor antagonist in inducing a lysosomal storage disorder phenotype (Department of Pharmacology, University of Oxford) Techniques learned: HPLC, TLC, Basic cell biology techniques, Toxicity (MTS) assays, DNA assays and Protein assays.
___________________________________________________________________________
EMPLOYMENT : RELIANCE CLINICAL RESEARCH SERVICES (30/06/2008-07/08/2009)
Role : Pharmacovigilance Associate/Medical Writer (Early and Advanced Development)
Conducted extensive feasibility surveys for the following indications :
- Osteoarthiritis
- Ulcerative Colitis
- Hyperlipidemia
- Cancer (Glioblastoma multiforme and Metastatic breast cancer)
- SAE reporting – Filling CIOMS and MedWatch forms
- Pharmacovigilance Associate for Corcept study conducted by Corcept Therapeutics, which investigated the role of mifepristone in reducing risperidone-induced weight gain. Responsible for :
- Maintaining the Adverse Event SAE tracker.
- Preparation of Project Safety File and Study Status report
Medical writing
- Wrote Investigator’s Brochure for DCGI submission
- Protocol for Bioequivalence studies for the following molecules :
- Lansoprazole
- Zidovudine
- Lamivudine
- Ropinirole
- Duloxetine
- Carbamazepine
- Fixed Dose Combination of Paracetamol+Diclofenac+Caffeine+Carisoprodol
- Carbamazepine multiple dose bioequivalence study
- Worked on an oncology Clinical Study Reports.
TATA CONSULTANCY SERVICES (17/08/2009-29/04/2011)
Role : Process Executive in the Drug Safety Division and currently working on the drug safety database and am also currently working on SAE reconciliation for several completed studies.
PRESENTATIONS :
2007 : Represented group in the Group-presentation competition at Oxford University and secured the first prize. The topic was “Polymorphism in Drug Metabolism”.
2006 : Was the leader of the Final year Chemistry project group presentation on Aspirin.
2005 : Was the leader for the group presentation on Human Rights Violations.
2008 : Presentation on Influenza Vaccine
2008: Early Development (Aspects of Study Details)
2008: Types of Study Designs in Bioequivalence Studies
2008: Parkinson’s disease and Ropinirole in the treatment of Parkinson’s
2009: Conducted a session for the Medical Affairs Department on the revised Declaration of Helsinki, Seoul, Korea, 2008
2009: Presentation on Multiple- Dose Bioequivalence Study template
2009: Presentation on Safety Reporting Timelines for the Corcept Study
2009: Presentation on Swine flu (Origin, How does it spread and Prevention)
2009: Trained the medical affairs team on the RECIST (1.0 and 1.1) criteria used in oncology trials.
ADDITIONAL SKILLS
IT: Microsoft Office Applications- Word, Excel, PowerPoint, ADI chart, Endnote. Worked on several safety databases.
EXTRA –CURRICULAR ACTIVITIES:
- Was captain of the Air Force Bal Bharati Junior Girls Basketball team (1997-1998).
- Was captain of the Jai Hind Junior College Girls Basketball team (2000-2001).
- Wrote for the St.Xavier’s Annual College newspaper (2004)..
- Took part in the Annual St.Xavier’s College Festival “Malhar” (2004).
- Was a part of a student organization in St. Xavier’s College called SAVE (Students against Violence and Exploitation, 2004-2006).
- Volunteered with other St.Xavier’s College students and helped in providing aid to victims in slum-areas devastated by the landslides during the July floods in 2005 in Mumbai.
- Represented St.Xavier’s College and won first prize in the Intercollegiate Chemistry Quiz competition in Mumbai (2006).
- Volunteered to teach at the Happy Home & School for the Blind (2005).
___________________________________________________________________________
COURSES ATTENDED:
- Home Office License Course (Modules 1-4) & holder of Personal License (Guinea-Pigs, Rats and Mice)
- GRE SCORE (11/05): VERBAL: 670/800
- QUANTITATIVE: 760/800
- TOTAL: 1430/1600
- TOEFL SCORE (11/28): 293/300
- ICH-GCP
- PHARCOVIGILANCE AND SAE REPORTING TIMELINES
- MEDICAL WRITING
- FEASIBILITY
REFERENCES AVAILABLE ON REQUEST.
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More Information about this submission and submitter:-
___________________________________________________
Submission ID : 4358012
Date & Time : 11th Jul 2011 1:13 PM (UTC)
IP Address : 27.4.33.102
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