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Hyderabad City Police Recruitment 2014

Hyderabad City Police Recruitment 2014- 150 Home Guard Posts: Hyderabad City Police, Home Guards Organization, Government of Telangana has announced notification for the recruitment of 150 Home Guard (Men) Vacancies. Eligible Citizen of India & must be local of Hyderabad City Police Unit can send their applications from 10-11-2014 to 22-11-2014 (excluding public holidays) in between 10:00 am to 02:00 pm. Other details like age limit, education qualification, selection process, application fee & how to apply are given below…
Hyderabad City Police Vacancy Details:
Total No. of Posts: 150
Name of the Post:
1. Home Guard (Men)
2. Technical (Drivers)

Age Limit: Candidates age should be between 18-50 years as on 29-10-2014.
Educational Qualification: Candidate should possess 7th class or equivalent examination (candidates who possess higher qualification than the prescribed will also be considered) & Valid LMV/ HMV license issued by the Govt.

Selection Process: Selection will be based on Physical Standard Test & Qualifying test of Driving.
Application Fee: Candidates has to pay Rs.25/- in cash should be remitted at the time of submission of each application form towards registration fee. There is no Fee for SC/ ST candidates.
How to Apply: Eligible candidates can send their application in prescribed format & Hall Ticket (in Duplicate) along with the copies of all necessary documents by hand to Goshamahal Stadium, Hyderabad on any working day between 10-11-2014 to 22-11-2014 (excluding public holidays) in between 10:00 am to 02:00 pm.
Last date for Submission of Applications: From 10-11-2014 to 22-11-2014 (excluding public holidays) in between 10:00 am to 02:00 pm.

For more details like age limit, educational qualification, selection process, application fee, how to apply and other information click on the following link …

Safety Medical Writer

  • Pharmacovigilance
  • Bangalore
Looking for Safety Medical Writers!

Are you looking for a job to unlock your Medical Writing skills? Apply for the position of Safety Medical Writer to have life changing career!

About the department
Novo Nordisk Service Centre India Pvt Ltd, responsible for the development of diabetes medicines. Novo Nordisk has a long and outstanding track-record of developing the best, most innovative and widely-used injection devices in the world. We are located at Bangalore.

The Job 
Be responsible for the planning and preparation of:
Development Safety Update Reports (DSURs)
Periodic Safety Update Reports (PSURs/PBRERs

Risk Management Plans (RMPs)
  • through development to submission
  • post-marketing
  • Responses to any safety questions raised in connection with assessment reports
Input to - investigational new drug applications (INDs), marketing authorisation applications (MAAs), new drug applications (NDAs), variations and supplemental new drug applications (sNDAs), and investigational medicinal product dossiers (IMPDs).
Other relevant ad-hoc documents
Contribution to knowledge sharing, skill building and good collaboration with stakeholders and colleagues:
You will also have an opportunity to participate in internal/external marketing/medical activities, e.g., expert meetings, lectures and conferences
Contribute to ongoing improvements in cross-functional and global collaboration and sharing of better practices and knowledge
Contribute to process improvements
Maintain up-to-date knowledge and competencies within relevant therapeutic and professional areas
Actively participate in relevant meetings, training sessions and seminars in the department, competency anchor and relevant project(s)

As Product responsible Safety Medical Writer, you will:
Act as mentor/trainer for other safety medical writers working with the product, as required.
Plan, drive, and co-ordinate preparation of documents to ensure submission according to the submission plan, or as otherwise agreed with Regulatory affairs.
Contribute to continuous resource planning process in collaboration with immediate superior – including identifying medical writing tasks and assist in the prioritisation of tasks
Perform consistency review of documents as back-up SMW
contribute to the evaluation of safety data from clinical trial and spontaneous sources 

Qualifications
Graduate (MSc, MBBS, BDS/MDS, B.Pharm/M.Pharm, B.V.Sc.&A.H or equivalent)

≥3 years of experience in Pharmacovigilance as Medical Writer/Pharmacovigilance writer/Advisor.
Experience with scientific writing in English (publications or equivalent)

Novo Nordisk is an organisation with many international employees. Here, you will get the opportunity to be a part of a global team that fosters great work culture, work independently and play an active role in the growth of the team through knowledge sharing and skill building and in addition enhance your career, benefiting from the possibilities for professional and personal development provided by Novo Nordisk.

At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and more than 371 million people worldwide need us. Working at Novo Nordisk is not just a way to make a living, but a way to make a difference.

Contact
For further information, contact Lavanya Sadashiva at +91 80 39988645

Deadline
1 December 2014

Career as Associate Project Manager @ Icon Clinical Research

ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development – from compound selection to Phase I - IV clinical studies ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.
Post: Associate Project Manager
Job Description:
Functions as primary contact to sponsors for assigned projects in the maintenance phase
Assists in the development of project related documentation.
prepares project summary report and analyses as needed
Assists in monitoring the quality within departments / projects
Assists callers to the IVRS Helpdesk
Candidate Profile
Background in Medicine, Science or other relevant discipline
Minimum of 2 yrs in IVRS or equivalent
Ability to manager multiple tasks and timelines
ability to prioritise tasks and delegated workload
ability to liase professionally with clients and system users
forien language skills desirable
Other responsibilities may be assigned as required.
Additional Information:
Education: Background in Medicine, Science
Location
: Chennai
Industry Type: Pharma/ Biotech/Clinical Research
Job Code: 011241
End Date: 30th Nov, 2014

Work as Analyst-Forecasting at Novartis - MBA with Graduate / Post Graduate in Pharmacy

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: Analyst-Forecasting

Job Description:
• Provide forecasting support to Novartis internal customers (CPOs & Regional marketing and sales teams) on various low-medium complexity forecasting reports.
• Support and facilitate data enabled decision making for Novartis internal customers by providing and communicating qualitative and quantitative analytics.
• Support GBS-GCO business in building practice by involving in various initiatives like knowledge sharing, on-boarding and training support, support team lead in all business related tasks / activities, building process documentation and knowledge repositories.
• Create and deliver below customer requirements as per agreed SLAs (timeliness, accuracy, quality, etc) and drive excellent customer service
o Strategic 5 year forecasts for in-line / pipeline products
o Lifecycle management forecasts for inline / pipeline products
o BD&L market & product revenue forecasts
o Pipeline product forecasts
o Monthly revenue forecasts by indication for 24 months
o Ad-hoc Forecasting support
• Deliver services through structured project management approach with appropriate documentation and communication throughout the delivery of services
• Support in creation and maintenance of standard operating procedures (SOPs), quality checklists that will enable excellent quality outputs for all outputs within the function
• Support in developing and maintaining knowledge repositories that captures qualitative and quantitative reports of brands, disease areas, macroeconomic trends of Novartis operating markets, etc
• Support team leaders in recruitment and on-boarding of new associates within the organization
• Participate in various knowledge sharing sessions that enables growth and improves quality of GCO Hyd deliverables across the function
• Comply with all internal functional operating procedures like time tracking, KPI tracking and reporting, and other internal systems and processes
• Comply to all Novartis operating procedures as per legal / IT / HR requirements.

andidate Profile:
MBA with Graduate / Post Graduate in Medicine (MD/MBBS/BDS) Pharmacy / Life Sciences Fluency in English is prerequisite, while knowledge of other in-scope country languages would be an advantage
- Experience (2-3 years) in forecasting in a market research firm or pharmaceutical company or Pharma KPO
- Should have an understanding of Pharmaceutical business including its regulatory environment
- Strong analytical thinking with problem solving approach
- Should have worked in an international company with exposure to working in cross-cultural environment
- Should be customer service oriented
- Strong and proactive business results-focus, and proven ability to provide insights that increase productivity
Additional Information:
Job ID: 153543BR
Experience: 2-3 Year
Industry Type: Pharma/Biotech/Clinical Research
Functional Area: other
End Date: 9th Dec, 2014