RGR SIDDHANTHI COLLEGE OF PHARMACY,
HYDERABAD, TELANGANA.
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Friday, February 19, 2016
RGR SIDDHANTHI COLLEGE OF PHARMACY, HYDERABAD, TELANGANA
Thursday, January 28, 2016
R.G.R Siddhanthi College of Pharmacy,Hyderabad Wanted Assistant Professor/Associate Professor
R.G.R Siddhanthi College of Pharmacy,Hyderabad Wanted Assistant Professor/Associate Professor
How to Apply: Interested and Eligible candidates may send their resume along with copies of certificates & recent passport size photograph,AADHAR card,PAN card to the following Postal address with in 10 days.
Contact Address:
RGR Siddhanti College of Pharmacy,
Bolton Road, Opp. Tivoli Garden,
Secunderabad – 500003
Phone: 27847370, 27898941
Email:scout_ap@yahoo.com
Tuesday, December 1, 2015
Help and advice on Manuscript preparation:
Help and advice on
Manuscript preparation:
Indo
American Journal of Pharmaceutical Sciences (IAJPS) provides paid services upon
the request by author. We help authors who face difficulty in writing an
article. You can just send the collected data; the rest will be done by us.
Cost of manuscript preparation will be informed to the author by email.
Submit
raw data through e mail to iajps.editor@gmail.com
Monday, November 30, 2015
Opportunity for Pharmacovigilance Leader in Novartis
Opportunity for
Pharmacovigilance Leader in Novartis
A global healthcare
leader, Novartis has one of the most exciting product pipelines in the industry
today. A pipeline of innovative medicines brought to life by diverse, talented
and performance driven people. All of which makes them one of the most
rewarding employers in their field.
Post: Pharmacovigilance Leader
Job
Description:
Performs
Pharmacovigilance activities for all assigned Novartis projects or products
including identifying and analyzing safety signals based on a comprehensive
evaluation of post marketing data and Serious Adverse Events (SAEs) from
clinical trials.
1. Monitors the clinical safety of projects/products and responds appropriately
2. Performs medical assessment and related activities for single cases, including collecting additional follow-up information as necessary, medical evaluation of quality defects, review of line listings of single cases, and preparation of investigator notifications.
3. Identifies safety signals based on the review of solicited or unsolicited single cases and confirm that they are not overlooked. Performs signal detection, monitoring and evaluation based on single cases, aggregate data and signal detection tools.
4. Provides input into responses to inquires from regulatory authorities or health care professionals on safety issues. Prepares safety data for health authority review boards. Provides input to responses for legal queries and CPO requests involving safety issues.
5. Provides Pharmacovigilance input to initial development of basic prescribing information and is responsible for Pharmacovigilance input into updates of this information.
6. Prepares medical input to aggregate clinical safety regulatory reports
7. Provides input to safety profiling and risk management plan
8. Provides guidance as appropriate to Clinical Safety Operations for the coding and causality/ expectedness assessment of adverse event reports.
9. Provides expert evaluation on the clinical context of adverse event reports, assessment on the medical conditions, and the implications on Novartis drugs.
10. Collaborates productively with colleagues from Clinical Research, Drug Regulatory Affairs, Medical Affairs, Medical Information, Statistics, Safety Data Management, Epidemiology and other related departments.
11. Participates in review of clinical study protocols/reports/other regulatory documents as needed.
12. Provides relevant input for IPT, ICT, and CTT meetings as needed.
13. Provides support as needed for licensing activities, regulatory authority inspections and for project/product recall activities.
Timeliness and quality of safety analyses, interpretations, and presentations
Compliance with internal and external regulations and procedures.
1. Monitors the clinical safety of projects/products and responds appropriately
2. Performs medical assessment and related activities for single cases, including collecting additional follow-up information as necessary, medical evaluation of quality defects, review of line listings of single cases, and preparation of investigator notifications.
3. Identifies safety signals based on the review of solicited or unsolicited single cases and confirm that they are not overlooked. Performs signal detection, monitoring and evaluation based on single cases, aggregate data and signal detection tools.
4. Provides input into responses to inquires from regulatory authorities or health care professionals on safety issues. Prepares safety data for health authority review boards. Provides input to responses for legal queries and CPO requests involving safety issues.
5. Provides Pharmacovigilance input to initial development of basic prescribing information and is responsible for Pharmacovigilance input into updates of this information.
6. Prepares medical input to aggregate clinical safety regulatory reports
7. Provides input to safety profiling and risk management plan
8. Provides guidance as appropriate to Clinical Safety Operations for the coding and causality/ expectedness assessment of adverse event reports.
9. Provides expert evaluation on the clinical context of adverse event reports, assessment on the medical conditions, and the implications on Novartis drugs.
10. Collaborates productively with colleagues from Clinical Research, Drug Regulatory Affairs, Medical Affairs, Medical Information, Statistics, Safety Data Management, Epidemiology and other related departments.
11. Participates in review of clinical study protocols/reports/other regulatory documents as needed.
12. Provides relevant input for IPT, ICT, and CTT meetings as needed.
13. Provides support as needed for licensing activities, regulatory authority inspections and for project/product recall activities.
Timeliness and quality of safety analyses, interpretations, and presentations
Compliance with internal and external regulations and procedures.
Candidate
profile:
Medical Degree
required. Specialty Board certification desirable. Useful additional degrees:
Post graduate degree in Pharmaceutical Medicine; Master of Public Health in
Epidemiology (or equivalent) Fluent in spoken and written English.
Understanding in another major language (e.g. French, German, Spanish)
preferred. 3 years clinical experience postdoctoral
· At least 3 years in drug development in a major pharmaceutical company including 2 years in drug safety at an operational or medical position
· Proven ability to analyze, interpret, discuss, and represent safety information both in writing and orally.
· Experience in preparing or contributing to preparation of clinical safety assessments and regulatory reports/ submissions involving safety information.
· Experience with (safety or others) issue management
· Experience in drug development, clinical trial methodology, regulatory requirements, scientific methodo logy, statistics and writing of publications
· At least 3 years in drug development in a major pharmaceutical company including 2 years in drug safety at an operational or medical position
· Proven ability to analyze, interpret, discuss, and represent safety information both in writing and orally.
· Experience in preparing or contributing to preparation of clinical safety assessments and regulatory reports/ submissions involving safety information.
· Experience with (safety or others) issue management
· Experience in drug development, clinical trial methodology, regulatory requirements, scientific methodo logy, statistics and writing of publications
Additional
Information:
Experience:
2-3 years
Industry
Type: Pharma/ Healthcare/ Clinical research
Functional
Area: R&D
Job
ID: 178579BR
Location: Hyderabad
Last Date: 25th December, 2015
Last Date: 25th December, 2015
MORE DETAILS Click on this link:
Friday, November 27, 2015
Thursday, November 26, 2015
Application are invited for Senior Research Fellow in Gokaraju Rangaraju College of Pharmacy
Application are
invited for Senior Research Fellow in Gokaraju Rangaraju College of Pharmacy
Gokaraju Rangaraju College of Pharmacy (GRCP) creates an
environment that opens up new worlds of opportunity. The institute is a DSIR
recognized Scientific and Industrial Research Organization (SIRO), accredited
by NBA, affiliated to Osmania University and approved by AICTE. Having four
research departments such as pharmaceutics, pharmaceutical chemistry,
pharmaceutical analysis and quality assurance and pharmacology, many research
staff and research scholars are contributing immensely to the scientific community.
GRCP has received research funding from DST, ICMR, AICTE and private Industries
such as Dr. Reddy’s laboratories, Laila Nutraceuticals, etc. GRCP has grown as
a premier institution in the field of Pharmacy Education and Research in India
and abroad. Alumni are well placed in India as well as abroad in various
pharmaceutical companies, government organizations like drug control, research
laboratories, etc., and in several well-known academic institutions.
Applications are invited from the eligible candidates to work as
Senior Research Fellow (SRF) in Indian Council of Medical Research (ICMR)
sponsored project no. DHR/HRD Fellow/Start up project/1/2013-14 under Dr.
Raghavendra N.M. at Department of Pharmaceutical Chemistry, Gokaraju Rangaraju
College of Pharmacy, Osmania University, Hyderabad.
Post: Senior Research Fellow (SRF)
No.of post: 01
Job Description
Candidates shall pursue drug design of novel Hsp90-BRAF
inhibitors by bioinformatic tools. The designed compounds to be synthesized
chemically and characterized by analytical parameters. Lead compounds would be
screened for in vitro cell proliferation assays and proteomics analysis of
Hsp90-client protein interactomes.
Candidate Profile
Candidate experience in molecular modeling, chemical synthesis, pharmacological screening including biochemical testing are encouraged to apply
Education: M.Pharm/ MS Pharm (Pharmaceutical Chemistry /Pharmacology/
Pharmacognosy/ Pharmaceutical Analysis).
Candidates with GPAT/CSIR-NET or equivalent examination qualification will be preferred.
Additional Information:
Experience: 0-5 years
Qualification: M.Pharmacy/ MS (Pharmacy)
Location: Gokaraju Rangaraju College of Pharmacy, Bachupally, Hyderabad, Telangana
Industry Type: Pharma/ Healthcare/ Clinical research
Duration: 3 years
Salary: Rs 18000 + 5400 = 23,400 per month
Functional Area: SRF
Interested candidate should send complete bio data to the
principal investigator, Dr. Raghavendra N.M (Email ID:nmraghav7@gmail.com; srf.grcp@gmail.com)
through email before15th December
2015.
Shortlisted candidates will be informed through Email and will be called for interview at Department of Pharmaceutical Chemistry, Gokaraju Rangaraju College of Pharmacy, Bachupally, Hyderabad.
The selected candidate will be allowed to register for Ph. D program of Osmania University as per Institute's procedure, subject to availability of seats and fulfillment of other essential criteria as per rule.
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