Tricks and Tips
Showing posts with label CAREERS. Show all posts
Showing posts with label CAREERS. Show all posts

Friday, August 7, 2015

Kudos to Pharm.D graduates for grabbing Government Jobs : List

Dear Readers..!!! Thanks for visiting my blog...!!!



Congratulations to all the Pharm.D graduates who got placed under Pharmacovigilance programme of India (PvPI) by Indian Pharmacopoeia Commission (IPC).

Here is the Result for the post of Technical Associates under PvPI from the personal interview held on 29th, 30th, 31st July and 01st August 2015 at IPC. 


Note: It is the list of selected candidates from both Pharm.D and M.Pharm

For more Updates, follow us on Facebook
Happy Blogging...!!!
Regards,
Deepak Kumar Bandari,
Pharm.D Intern,
Vaagdevi College of Pharmacy - India
Elsevier Student Ambassador - South Asia

Patent Analyst : Research and Development - Novozymes

Dear Readers..!!! Thanks for visiting my blog...!!!

Patent Analyst, Intellectual Property, Research & Development
Location: Bengaluru, India
Last Date: 18- August 2015
Company Profile:


At Novozymes, we work in close partnership with our customers to make an impact and help create a better world. We use science to advance industries, and as part of R&D, you will create and develop the biological answers that will pave the way for a brighter future.
You’ll be part of a dynamic international team of patent analysts and attorneys based in Bengaluru and other locations across the world, and will assist in delivery of quality results in search and analysis domain within intellectual property. 
You thrive in a fast-paced learning environment and are as comfortable with working in a team by coordinating with other analysts and attorneys on a day-to-day basis as you are with working independently with attention to detail - interpreting data, performing analysis and presenting results. For the right individual, this is a fantastic career opportunity with potential for personal and professional development.

Requirements:
  1. Have a Master’s degree with relevant experience within biotechnology, biochemistry, or molecular biology, possibly supplemented with a PhD
  2. You should have 2-4 years of experience working as a Patent analyst or in a similar role – especially in making excellent searches and informative reports
  3. Have expertise in working with Freedom to Operate Analysis (FOA) and clearance searches (added advantage)
  4. Be a team player with strong analytical, documentation and communication skills
  5. Be able to work independently and take ownership
  6. Be creative, take initiative, learn fast, display result orientation and work with challenging deadlines
How to apply: Click here

For more Updates, follow us on Facebook
Happy Blogging...!!!
Regards,
Deepak Kumar Bandari,
Pharm.D Intern,
Vaagdevi College of Pharmacy - India
Elsevier Student Ambassador - South Asia

Thursday, August 6, 2015

Clinical Trial Monitor - Phase Studies : Manipal Acunova Ltd

Dear Readers..!!! Thanks for visiting my blog...!!!

Clinical Trial Monitor - Phase Studies : Manipal Acunova Ltd

Role : Clinical Research Associate / Scientist
Number of Openings : 03
Experience required : 1-4 years 

Location : Bangalore


Ecron Acunova provides end-to-end services for Phase I-IV clinical research, including Clinical Trial Management, Clinical Data Management, PK/PD services and Central Lab. Ecron Acunova has research facilities in Asia as well as an established presence in various parts of Europe and the United States. We offer clinical development services to the pharmaceutical, biotechnology, nutritional, device and medical diagnostics industries. Our service quality, therapeutic expertise and global reach have allowed us to grow rapidly, building a list of demanding clients. We provide an attractive package of services coupled with the ability to rapidly conduct clinical trials utilizing a world class delivery platform.


Job profile: 
The responsibility is to perform all clinical monitoring aspects of designated projects in accordance with applicable SOP and regulations. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, and data collection), collecting regulatory documentation (when required), performing qualification, initiation, monitoring and termination of investigational sites in accordance with ICH-GCP guidelines.

  1. Preparation of Site feasibility questionnaire, conducting the feasibility and reporting to PM.
  2. Preparation, conduct and reporting of site selection visits.
  3. Negotiation & obtaining Investigator agreement on site budget, payment to the sites.
  4. Development/Local adaptation of study specific documents (ICF, CRF prints, Study logs), translations of the documents.
  5. Procuring essential documents from sites, their QC and filing in a timely manner and updating project tracker or sending the documents to PA for filing in a timely manner.
  6. Maintenance of TMF and Site specific file.
  7. Scanning & uploading documents into shared drive.
  8. Transmission of documentation into project files.
  9. Preparation of regulatory dossier, regulatory submission and follow-up.
  10. Preparation of EC dossier, EC submissions and follow-up.
  11. Co-ordinating arrangements for the investigators meeting, acting as a host for this meeting.
  12. Development of meeting materials along with required presentations for investigators meeting.
  13. Site initiation visit planning, preparation, conduct, report and follow-up of pending issues.
  14. Co-ordinating the IP request between sites and pharmacist/ vendor/ sponsor. 
Desired Candidate Profile :

UG : B.Pharma - Pharmacy, PG : M.Pharma - Pharmacy, Doctorate : Any Doctorate - Any Specialization, Doctorate Not Required


Worked in Ophthalmology or Oncology studies Clinical Studies I-IV
  1. Ability to interact professionally with clients/vendors.
  2. Excellent interpersonal, verbal and written communication skills and ability to work in a team.
  3. Effective time management skills and prioritize tasks to manage study timelines.
  4. Strong computer and internet skills including knowledge of MS-Office products such as Excel, Word etc, sound presentation skills.
  5. A minimum of 65% on average.

Recruiter Name : M. Chaarumathi

For more Updates, follow us on Facebook

Happy Blogging...!!!
Regards,
Deepak Kumar Bandari,
Pharm.D Intern,
Vaagdevi College of Pharmacy - India
Elsevier Student Ambassador - South Asia

Drug Safety Associate - Clinical Development : Dr.Reddy's

Dear Readers..!!! Thanks for visiting my blog...!!!

Drug Safety Associate, Clinical Development - Dr. Reddy's



Role : Drug Safety Associate, Clinical Development
Number of Openings : 01
Experience required : 1-3 years in Pharmacovigilance operation
Location : Hyderabad


Dr. Reddy's Laboratories Ltd. is an integrated global pharmaceutical company, committed to providing affordable and innovative medicines for healthier lives. Through its three businesses - Pharmaceutical Services and Active Ingredients, Global Generics and Proprietary Products - Dr. Reddy's offers a portfolio of products and services including APIs, custom pharmaceutical services, generics, biosimilars and differentiated formulations. Major therapeutic focus is on gastro-intestinal, cardiovascular, diabetology, oncology, pain management and anti-infective. Major markets include India, USA, Russia-CIS and Europe apart from other select geographies within Emerging Markets. 

For more information, log on to: www.drreddys.com

Job Profile: 

1. Assimilate information on adverse events, perform initial checks, update safety data tracking tool, do case validation, preliminary assessment of case reportability and create case report file.

2. Ensure complete and consistent data entry of adverse event reports from source documents with acceptable timeline and quality.

3. Manage handling of non-expeditable AE reports, legacy AE reports including review for completeness and accuracy.
4. Use medical dictionaries and business guidance to check correct coding of medical history, drugs and adverse event terms.
5. Identify clinically relevant information missing from case report and facilitate its collection (from medical team) to generate appropriate follow-up request as needed.
6. Alert manager about important safety concerns based on preliminary case reports.
7. Work with drug safety team to ensure high compliance for end to end ICSR management.
8. Work with drug safety team in various safety data related administrative and procedural activities as required or requested.

Educational Qualification :  Masters Degree in life sciences or related fields; or equivalent.

Professional requirement :
  1. Good understanding and experience of adverse event cases processing (ISCRs) from various sources such as Spontaneous, Post marketing surveillance Studies, Published Medical Literature, Health Authority/ Legal notification & Clinical Trials etc.
  2. This includes primarily, case processing, coding of events, medical history and drugs, narrative writing etc.
  3. Familiarity and general understanding of medical terminology, experience in working with medical dictionaries (MedDRA & WHO DDE).
  4. Good understanding of pharmacovigilance, Global and local regulatory reporting requirements, etc.
  5. Experience with working on Global standard safety data bases such as ARISg and/or Argus safety.
  6. Basic understanding of clinical trials procedure.
  7. Good ability to ability to write good English or communicate.
  8. High commitment for compliance.
  9. Sense of urgency and commitment for timely completion of activities.

For more Updates, follow us on Facebook

Happy Blogging...!!!
Regards,
Deepak Kumar Bandari,
Pharm.D Intern,
Vaagdevi College of Pharmacy - India
Elsevier Student Ambassador - South Asia

Manager - Medical Monitoring : Dr. Reddy's

Dear Readers..!!! Thanks for visiting my blog...!!!




If you see an opportunity you would like to explore further, do write in to us with your CV on careers@drreddys.com.

For more Updates, follow us on Facebook

Happy Blogging...!!!
Regards,
Deepak Kumar Bandari,
Pharm.D Intern,
Vaagdevi College of Pharmacy - India
Elsevier Student Ambassador - South Asia

Walk in for Clinical and Project Management - Quintiles


Dear Readers..!!! Thanks for visiting my blog...!!!


Walk in Event for Clinical and Project Management - Aug 8 2015 in Quintiles - Bengaluru 

Role: Clinical Research Associate / Scientist

Number of Openings : 50

Experience required : 1-6 years

LocationQuintiles, Etamin Block, Wing A, Prestige Tech Park II, Outer Ring Road, Sarjapur, Bangalore - 560103
Date : 8 - August 2015, 08:00 am
Documents to carry : CV, last 3 months pay slip, id proof
Interview processAssessment process - CV screening- Aptitude tests- HR Interview- Technical interview- Final interview.
Salary 2,50,000 - 7,50,000 P.A

Company profile: Quintiles is the world's largest provider of biopharmaceutical development and commercial outsourcing services. We bring a fully integrated approach to build biopharma and life sciences solutions - from pipeline through portfolio to population health. A career with Quintiles connects you to great opportunity to achieve professional success and impact healthcare around the world.

More details: 

1. Clinical Research Professionals Candidates with 1-8 years of experience in clinical research field.
2. Records Management Professionals Candidates with 2-6 years of working in the field of clinical research or in a parallel lead role. Strong ability to identify clinical research documents. Knowledge of systems, databases and software programs. 
3. Project Management professionals Candidates with 5+ years of experience in project management preferably in clinical / healthcare domain. 

Desired Candidate Profile :

Education:

UG : Any Graduate - Any Specialization, B.Pharma - Pharmacy, BDS : Dentistry

PG : Any Postgraduate - Any Specialization, Post Graduation Not Required

Doctorate : Any Doctorate - Any Specialization, Doctorate Not Required

Contact number91-80-41384900

For more Updates, follow us on Facebook

Happy Blogging...!!!
Regards,
Deepak Kumar Bandari,
Pharm.D Intern,
Vaagdevi College of Pharmacy - India
Elsevier Student Ambassador - South Asia

Message to Indian Pharmacists: Opportunities in the Global Market

Dear Readers..!!! Thanks for visiting my blog...!!!

I'm very much thankful to His excellency Lt. Colonel PRASAD R TIRUNAGARU M. Pharm., MSC, R.PH for sharing this valuable information with us.

Lt. Colonel Prasad received his B.Pharm and M.Pharm degrees from Andhra University and Medical Service Core training as a combat pharmacist at the Academy of Health Sciences of US Army Medical department centre, Texas, USA. He was the first South Indian to be commissioned as an officer in the US Army. He was the first foreigner to pass the prestigious California State Board Exams in the world.

He has thirty five years of experience as a registered pharmacist in USA, as Assistant Chief and Chief of Pharmacy in various army medical centres. Specialties include clinical research in developing human genetic insulin, nutritional studies, in-patient and outpatient pharmacies, oncology, chemotherapy and nuclear pharmacies. Developed hospital formulary, clinical training modules for healthcare professionals.


Message to Indian Pharmacists: 


US Job Market: There is always great demand for registered pharmacists in USA, the pharmacists are highly respected, most trusted and well paid professionals. The average salary is $120,000 to $200,000 per year. 

Retail and Community Pharmacist: It provides majority of the pharmacist jobs in USA. The major function of the pharmacists is filling and dispensing medications by reviewing and interpreting physician orders, detecting therapeutic incompatibilities. They counsel the patients regarding drug usage, side effects and precautions, they also administer vaccines and drug information. They help physicians and healthcare professionals regarding proper usage, selection of medications and therapeutic guidelines. 

Hospital Pharmacist: Pharmacists play a very important role as a healthcare team member in the hospital providing high quality comprehensive pharmaceutical care. Specialties include outpatient pharmacy, inpatient pharmacy, oncology/IV Admixture. They dispense all required medication to the wards for patient administration. They provide clinical drug data, therapeutic information to all medical team members, monitor drug reactions and patient profiles. They help patients with drug counselling to optimize therapy. 

Clinical Pharmacist: Clinical pharmacists play a vital role in the applied therapeutics; they require 1-2 years of specialized programmes and training in various specialties, i.e., ambulatory care, internal medicine, pediatrics, psychiatry, geriatrics. They are well paid. They are part of every medical and therapeutic team in the hospital. Recently, State Provider Statues Bill became law in many US states. The Legislation provides that “A pharmacist may perform any patient care service delegated to the pharmacist by a physician”.


Industrial Pharmacist:This is a very promising field, specialties include drug discovery, drug development, manufacturing, clinical trials and marketing. Now, there is an exciting new world bioinformatics, genome therapy, stem cell research and promising nano-technology. 

Regulatory Authorities: US Food and Drug Administration and State Boards of Pharmacies have special and important jobs. FDA has several mission-critical medical and science positions at biological evaluations, drug evaluation and research, food safety, applied nutrition, toxicological research and drug inspectors, drug regulatory authorities at various state boards.

Immigration to USA: The important step is getting an immigrant visa to enter into USA. The choices are go for higher education or PhD in various universities. The other one is getting a dependent visa.

State Board Exams: All foreign graduates must obtain certification by the Foreign Pharmacy Graduate Equivalency Committee (FPGEC) before they can get an intern pharmacist licence. They must pass Foreign Pharmacy Graduate Equivalency Exam. In order to practice as a registered pharmacist, you have to pass the North American Pharmacists Licensure Examination (NAPLEX). Rules vary from state to state, please check individual state websites.

Tips for Passing Board Exams

Pharmacy Law: It is a very important part of the State Board Exam. Laws are very strict and precise; each state has its own state board of pharmacy laws. 

Pharmacy Mathematics: Our students can easily get 100% , mostly drug dosing conversions, drug percentage calculations and drug formulations etc. 

Drug Identifications: They must be able to identify important medications by color, shape, markings on tablets. PDR has all the information. 

Trade and Generic Names: They need to learn generic and trade names for the top 200 drugs and more. 

Drug Interactions: It is very important to know pharmacological actions of various important drugs, their medicinal chemistry, actions on target organs, drug metabolism, excretion and side effects. 

Drug and Food Interactions: They have to know food and drug interactions of all critical drugs. 

Clinical Pharmacy: It is a very critical part of patient case studies, patient profiles and interpretation of clinical laboratory tests and adverse drug reactions.


For more Updates, follow us on Facebook

Happy Blogging...!!!
Regards,
Deepak Kumar Bandari,
Pharm.D Intern,
Vaagdevi College of Pharmacy - India
Elsevier Student Ambassador - South Asia

Wednesday, May 27, 2015

Public Health Research Initiative (PHRI) Research Grant: 2015-16

Dear Readers..!!! Thanks for visiting my blog...!!!

Dear Pharm.D Professionals,

Finally, the wait is over now its time to prove.. This is a challenging opportunity to prove the strength of Indian research in Global Public Health, If we get succeed in this.. there exists many more opportunities. 
All the Best.

Public Health Research Initiative (PHRI)

Public Health foundation of India (PHFI) in collaboration with Science and Engineering Research Board (SERB, A Statutory Body under Department of Science and Technology (DST)) aims to set up an extramural fund to provide the Indian researchers focused on public health from institutions of repute, as per an established process. PHRI will enable young Indian researchers to carry out clearly defined research project at a place of their choice up to a period of 36 months.

Project Duration and Cost:

These grants will be awarded for research studies of public health importance in India. The estimated amount of the available research grant is limited to 30 Lakh INR per fellowship. The total duration of the grant will not exceed more than THREE years.

Eligibility Criteria:

The applicant must possess a Postgraduate degree from an accredited institution in any domain related to public health, including medical and non-medical sciences, nutrition, physiotherapy, dentistry, pharmacy, nursing, social sciences, law and humanities. It would be desirable if the applicant has a doctoral degree. (Applications related to Biomedical, Biophysics and biochemistry are excluded from PHRI fellowships)

Age Criteria:

The applicant must be40 years or less at the time of applying for the PHRI Research Grant, age relaxation of 5 years is applicable for female or if applicant belong to SC/ST/OBC then

Application procedure:

Candidates are requested to apply online

a) Online application formats with detailed guidelines are available at the website www.phfi.org Guidelines for Submitting a proposal
This should include the following:
Title of the study
Overall goal
Broad Objective
Specific objectives
Methodology
Analysis plan
Expected outcome
Timeline
Implications for future research
References
Dissemination and publication plan
Itemized budget along with justification for each item
Curriculum vitae of investigator listed in the grant application

Word limit: Not more than 3000 words (excluding references, Dissemination plan, Itemized budget and Curriculum Vitae) Font Style: Times New Roman Font Size: 12 with Line Spacing 1.5

Kindly note following should be mentioned while sending the grant application:

Area of work:

Area proposed by candidate should be clearly defined research area in any aspect of Public Health like Public Health Nutrition, Non Communicable Diseases, Infectious Diseases and Public Health Policy etc.

Place of work:

A project site in India, depending on the demand of the research study. The PHFI reserves the right to reject the fellowship application in case candidate DOES NOT FULFIL minimum qualification or supplies any false information.

Public Health Research Initiative (PHRI) Fellowship: 2015. Online submission will close by 15 June 2015 after 5:00 PM.

Click here to apply for Grants

For more Updates, follow us on Facebook

Happy Blogging...!!!
Regards,
Deepak Kumar Bandari,
Pharm.D Intern,
Vaagdevi College of Pharmacy - India
Elsevier Student Ambassador - South Asia

Vacancies as Junior Medical writer in Medeka Health

Dear Readers..!!! Thanks for visiting my blog...!!!

Medeka is a professional media group focused on the health sector. It is an information services group, specialized in connecting health communities across strong inter-portable platforms of digital, print and live events. We are constantly innovating and exploring newer dimensions to promote enterprise, enhance knowledge and provoke action. Our proximal client base includes the pharmaceutical & allied healthcare marketers, medical professionals and patients/consumers. With delivery capabilities in Middle east, China, Hong Kong, Singapore and Taiwan and other SEA countries, our aim is to emerge as a leading regional player in the healthcare ICT sector We specialize in connecting communities through strong inter-portable channels in print, live events and digital platforms. Our proximal client base includes the pharmaceutical & allied healthcare marketers, medical professionals and patients/consumers.

Position: Junior Medical writer

Job Description:

The Medical Writer is responsible for researching, writing, and editing monographs, booklets, review articles, slide kits, LBLs, compendium for the pharmaceutical industry.

Job responsibilities:
  1. Understanding requirement of the clients
  2. Conducting reference searches
  3. Writing articles suiting to the requirement.
  4. Reviewing and amending work in response to feedback
  5. Communicating with designers and business development executives
  6. Delivering projects meeting minimum standards
Skills Required:
  1. Good medical and pharmacology knowledge
  2. Analytical and interpretation ability
  3. Basic writing competency
  4. Ability to generate ideas and interpret complex documentation
  5. Ability to learn quickly and manage a high volume workload
  6. Creativity
  7. Interpersonal and relationship attributes
  8. Organizational and multitasking capabilities
Additional Information:

Qualification: M.Pharm, Pharm.D
Location: Bangalore
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Medical Writing
End Date: 30th May, 2015

Forward your professional resume attested with  a cover letter to: vishva.matad@medekahealth.com

For more Updates, follow us on Facebook

Happy Blogging...!!!
Regards,
Deepak Kumar Bandari,
Pharm.D Intern,
Vaagdevi College of Pharmacy - India
Elsevier Student Ambassador - South Asia

Tuesday, May 26, 2015

Vacancies in Novartis as Pharmacovigilance scientist


Dear Readers..!!! Thanks for visiting my blog...!!!


Novartis is a world leader in the research and development of products to protect and improve health and well-being. The company has core businesses in pharmaceuticals, vaccines, consumer health, generics, eye care and animal health. Headquartered in Basel, Switzerland, Novartis employs nearly 1,15,000 people in over 140 countries worldwide to help save lives and improve the quality of life.

Eligibility: Life sciences degree /Nursing background Good knowledge/fluency in English. Knowledge of other languages desirable. Experience in drug safety / Development or closely related areas of responsibility Experience of safety document writing Good negotiation and oral communication skills will be an added qualification.

Job description: 

  1. Evaluation and QC of Serious Adverse Event / Post Marketing Adverse Event to ensure accurate and consistent data entry and processing from source documents, with emphasis on timeliness and quality.
  2. Ensure accurate and consistent coding of medical history, drugs and adverse event terms.
  3. Assess adverse event reports for seriousness, causality and expectedness as per the Investigator Brochure/Basic Prescribing Information/US package insert, consulting the Medical Safety Expert whenever needed.
  4. Determine the necessity for follow-up and prepare follow-up request as needed.

Other responsibilities:
  1. Evaluation and QC of Serious Adverse Event / Post Marketing Adverse Event to ensure accurate and consistent data entry and processing from source documents, with emphasis on timeliness and quality.
  2. Ensure accurate and consistent coding of medical history, drugs and adverse event terms.
  3. Assess adverse event reports for seriousness, causality and expectedness as per the Investigator Brochure/Basic Prescribing Information/US package insert, consulting the Medical Safety Expert whenever needed.
  4. Determine the necessity for follow-up and prepare follow-up request as needed.
  5. Work in conjunction with Clinical Safety Associates, Clinical Safety Scientists from other processing sites and Medical Safety Physician (Pharmacovigilance Leader and Brand Safety Leader) to ensure that reports are accurately evaluated and databased.
  6. Triage literature cases for databasing or pass them on to the Team Leader for approval of rejection.
  7. Co-author, together with the Medical Safety Physicians, all required regulatory periodic reports, collecting, organizing and presenting the available data.
  8. Work with external partner groups, e.g. co-licensing partners and Clinical Research Organisations to meet joint accountabilities
  9. Represent DS&E at internal and external meetings
  10. Assist the Medical Safety Physicians with project activities in specific therapeutic areas, compatible with the timely processing/production of individual case reports and regulatory periodic reports.
  11. Assist the Medical Safety Physicians in monitoring the safety profile of product
  12. Be involved in development and testing of safety systems/IT applications and in the preparation of relevant manuals.
  13. Participate in cross-functional teams on safety matters/DS&E special projects relating to investigational and marketed drugs Impact on the organization.
  14. Ensure that Serious Adverse Event / Post Marketing Adverse Event are evaluated accurately and within the required timeframes to meet regulatory requirements.
  15. Alert the Medical Safety Physicians to potential safety issues.

For more Updates, follow us on Facebook

Happy Blogging...!!!
Regards,
Deepak Kumar Bandari,
Pharm.D Intern,
Vaagdevi College of Pharmacy - India
Elsevier Student Ambassador - South Asia