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Showing posts with label VACANCIES. Show all posts
Showing posts with label VACANCIES. Show all posts

Friday, February 19, 2016

Drug Safety Associate at Covance - Freshers

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Manage the receipt and processing of all adverse event reports reported either spontaneously from any source or from a clinical trial. This includes, but is not limited to: 
Entry of safety data onto adverse event database(s) and tracking systems
Review of adverse events for completeness, accuracy and appropriateness for expedited reporting.
Write patient narratives
  • Code adverse events accurately using MedDRA
  • Determine expectedness/listedness against appropriate label
  • Identifies clinically significant information missing from initial reports and ensures its collection
  • Ensure case receives appropriate medical review
  • Prepare follow-up correspondence consulting the medical staff accordingly.
  • Ensure all cases that require expediting reporting to worldwide regulatory agencies are processed swiftly and appropriately within required timelines
  • Reporting of endpoints to clients, regulatory authorities, ethics committees, investigators and Covance project personnel, if required, within study specified timelines.
  • Maintain a strong understanding of Covance’s safety database conventions or client specific database conventions, as appropriate.
  • Begin participating in signal detection and trend and pattern recognition activities, as appropriate.
  • Begin preparing timely pharmacovigilance reports for products and safety issues, including Individual Case Summary Reports (ICSRs) of Serious Adverse Events
  • Assist in the preparation of listings for Annual IND reports, Periodic Reports (PRs) and Periodic Safety Update Reports (PSURs).
  • Work with Data Management or client on reconciliation of safety databases.
  • Begin participating in the generation of monthly status and other project-specific reports ensuring the quality and accuracy of metrics and data provided.
  • Support/train less experienced safety staff in all aspects of case-handling, adverse event reporting.
  • Maintains a comprehensive understanding of Covance Safety’s Standard Operating Procedures (SOPs), Work Instructions (WI), guidance documents and directives associated with safety management, reporting and pharmacovigilance.
  • Possess knowledge of other procedural documents, e.g., SOPs, etc. that impact Safety.
  • Ensure compliant safety reporting in accordance with US and international reporting regulations, SOPs and safety processing guidelines set forth by departmental management team and the client.
  • Build and maintain good PV&DSS relationships across functional units.
  • Demonstrate role-specific Competencies on a consistent basis.
  • Demonstrate company Values on a consistent basis.
  • Begin to develop a good knowledge of contract assumptions; identifying out of scope work.
  • Read and understand Safety Management Plans (SMPs), Reconciliation Plans, and other safety-specific plans ensuring optimal efficiency.
  • Begin participating in Covance project teams and client meetings as appropriate.
  • Assist in the review of cumulative safety data for submission to Drug Safety Monitoring Boards (DSMBs), regulatory authorities or clients.
  • Assist with the set-up of, and the provision of data to, Safety Committees/DSMBs.
  • Assist in the co-ordination of endpoint committees, as required.
  • Any other duties as assigned by management.
Education Required:
• Non-degree + 4-5 yrs relevant experience (or 2 yrs safety experience)*
• Associates Degree + 3-4 yrs relevant experience (or 1-2 yrs safety experience)*
• Associate degree RN + 2-3 yrs relevant experience (or 1-2 yrs safety experience)*
• BS/BA + 1-2 yrs relevant experience**
• MS/MA + 0 yr relevant experience**
• PharmD + 0 yrs relevant experience**


Degree preferred to be in one or more of the following disciplines: Biological Sciences, Pharmacy, Nursing, Life Sciences, and Chemistry.
*Safety experience includes actual experience processing AE/SAE reports, generating narratives, queries, working within safety databases, and experience with regulatory submissions.
**Relevant experience includes experience in the pharmaceutical, biotechnology, or CRO industry, partly in related areas such as Medical Affairs, Clinical Data Entry and Clinical Data Management, Clinical Data Monitor, Regulatory Affairs, or Quality Assurance.
• Speaking: English and local language.
• Writing/Reading: English and local language.


Experience Required:
• High degree of accuracy with attention to detail.
• Functions as a team player.
• Good Communication.
• Knowledge of medical and drug terminology desirable.
• Familiarity of Good Clinical Practice (GCP) related to clinical safety documentation.
• Familiarity with ICH Guidelines
• Familiarity of worldwide regulatory requirements and reporting of adverse event for both marketed and investigational products.
• Familiarity of worldwide regulatory requirements and reporting of adverse event for both marketed and investigational products.
• Good written and verbal communication skills.
• Ability to work independently with moderate supervision.
• Good keyboard skills, preferably with knowledge of MS office and Windows would be beneficial.

Apply Here

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

Pharmacists Wanted for Dubai

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Urgent requirement of Pharmacist for retail shops in Dubai for male candidates.
Qualification: B.Pharm, M.Pharm, MSc, BSc chemistry are eligible with or without experience.
Salary : AED 3000.00 for six months.
After DHA exam salary will be AED.5000.00
After one year salary will be AED.6000.00
MSc & BSc salary AED.3000.00
Free accommodation, free transportation & free medical benefits.
Mode of selection : CV
Contact number: 9037669901
Salary: INR 5,50,000 - 7,50,000 P.A

Desired Candidate Profile: Education- UG: B.Sc - Any Specialization, Chemistry, PG: M.Sc - Any Specialization, Chemistry. Doctorate: Any Doctorate - Any Specialization, Doctorate Not Required

Company Profile:


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

Pharmacist -Fortis Hospital : Fresher

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Job description: 
Issue & Return of Material against Patient indents from Stores and against Departmental indents.
Direct Issue of drugs/ medical consumable to Patient
Issue of Narcotics as per protocols
Receiving the material at Receiving Bay & Processing of Invoices.
Emergency Cash Purchase.
Receipt of consignment goods & Processing their Invoices on Consumption.
Physical Stock Verification.
Sale & return of material in OP Pharmacy.
Drug Expiry control and checking expires of medicine before dispensing to patients.
**Karnataka State Pharmacy Council Registration is mandate.

Role:Pharmacist/Chemist/Bio Chemist

Number of Openings: 5
Desired Candidate Profile: Education- UG: B.Pharma - Pharmacy, Diploma - Any Specialization. PG: M.Pharma - Pharmacy. Doctorate: Doctorate Not Required
Company Profile: Fortis Healthcare Ltd
Fortis Healthcare Limited is committed to clinical excellence and patient-centric healthcare, which is manifest in hospital design, patient services, medical programmes and the compassionate approach of medical and non-medical hospital staff. Fortis commissioned its first hospital in 2001 at Mohali, near Chandigarh, and has expanded its operations to become a network with an over 10,000 bed capacity across 68 hospitals.
Recruiter Name: Monika Priyadarshini
Contact Company: Fortis Healthcare Ltd
Telephone: 080-41994493

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

Tuesday, December 22, 2015

Clinical Data Manager in Novartis : B.Pharm

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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: Clinical Data Manager

Job Description: Provide timely and professional ongoing management of clinical trial data with respect to cost, quality and timelines for assigned trials managed within Clinical Data Management. Ensure consistently high quality data available for analysis and reporting.
1. As Clinical Data Manager (CDM) provide data management input on Clinical Trial Teams. May have the role of TDM on small, low complexity trials
2. Reviews and contributes to preparation of protocols, specifically related to the Visit Evaluation Schedule (VES), Study Design and Data Management section
3. Gives input to Data Handling Plan (DHP) and Data Review Plan (DRP) for assigned trials. Responsible for the development of these documents if assigned the role of Trial Data Manager (TDM)
4. Participates in the preparation of training materials for investigator meetings
5. Disseminates study-level information either to the TDM (if assigned to a trial as a Data Manager) or to the Clinical Trial Team (CTT) & Program Clinical Data Manager (PCDM) if assigned the role of TDM
6. Performs DM activities for start-up of a study including preparing the eCRF, CCGs, DHPs, DRPs and performing User Acceptance Testing (UAT) if required
7. Obtains input from study team members on the design of clinical databases while ensur-ing data quality and compliance with SOPs (if assigned the role of TDM)
8. Under supervision from PCDM (or delegate), ensures consistency of assigned trials with program level standards (DHPs, DRPs & eCRFs) Prepares final study documentation.
9. Performs ongoing review of all data generated from the clinical study including central and local lab data and coding
10. Interacts with the study team members to define the necessary listings needed to support data validation
11. Performs review of listings for quality, content, format and output
12. Identifies possible trends in data Leads and participates in the final review of all data generated from the clinical study
13. Participates in the preparation (if assigned as DM level) or prepare final study documentation
14. Performs final review of listings for quality, content, format and output
15. Performs activities necessary for database finalization and adhering to the timelines es-tablished by the study team
16. Verifies and tracks eCRF/CRF completion and provide data status updates
17. Ensures appropriate Novartis tracking systems are up to date and accurate
18. Actively participates at the study team level
19. Utilizes status and metric reports to identify training needs and issues with investigator sites
20. Gathers requirements for third party data
21. Maintains effective working relationships with Contract Research Organization (CRO) and other vendors as required

Candidate Profile: University or college degree in life science, computer science, pharmacy, nursing or equivalent relevant degree Fluent English (oral and written). Ideally 3 years’ experience in Drug Development with at least 2 years in Clinical Data Management

Additional Information:
Location: Hyderabad
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: R&D
End Date: 25th January, 2016


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

Vacancy in Drug resistant Breast Cancer project at NIN

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NIN has attained global recognition for its pioneering studies on various aspects of nutrition research, with special reference to protein energy malnutrition (PEM). Institute’s activities are broad-based, encompassing the whole area of food and nutrition. The Institute has achieved close integration in its research activities between the laboratory, the clinic and the community.

Name of the post/ position: Junior Research Fellow


Eligible candidates are invited to apply for the following post/ position on the ad hoc research project entitled: "Drug resistant Breast Cancer Cells to understand Cancer Stem Cells metabolism and therapy" funded by DBT at this Institute.

Applications will be received from the individuals on 5th January, 2016 between 9:30 A.M. and 10:30 A.M. at Conference Hall, NIN, Tarnaka, Hyderabad. Late applications will not be entertained after 10:30 A M under any circumstances. The Candidates may download Application form from NIN website.

The essential qualification, experience, consolidated Pay and service tenure are as under:
Essential Qualifications: Post Graduate Degree in Basic Science with NET qualification or Graduate Degree in Professional Course with NET qualification or Post Graduate Degree in Pharmacy from recognized University.
Desirable: Masters in Pharmacy or Bachelor in Pharmacy with GATE or GPAT exam qualifying score or M.Sc. in Biochemistry/ Biotechnology/ Life Science with NET qualifying score.

Age: Below 30 years. Relaxation of age is admissible as per G O.I. Rules.
Consolidated Stipend/ Emoluments: Rs. 12,000.00 + 30% HRA per month fixed without any other allowances.
Tenure: Initially for one year and extendable based on performance and funds position.

Date & Time of Written Test/ Interview: 5th January, 2016 from 9:30 A.M. onwards.

The shortlisted candidates should bring all original certificates of educational qualification (from SSC onwards), experience, SC/ST/OBC Community Certificate/ PH Certificates along with a pass port size photograph and set of Photo copies duly attested for attending the Written Test/ Interview. The persons belonging to Other Backward Category should bring the latest O.B.C. (Non-creamy layer) Certificate issued by the respective Tahsildar/ MRO specifically issued for the purpose of applying for Central Government Post. No TA/ DA will be paid for attending the Written Test/ Interview.

GENERAL CONDITIONS: The conditions of employment will be the same as that for the project staff on contract basis. The candidates have no right to claim for any regular employment at this Institute. The Director in-charge & Appointing Authority has the right to accept/ reject any application without assigning any reason/s and no correspondence in this matter will be entertained. Age, experience etc., will be reckoned as on 14 12.2015.

Selection Procedure: Written test/Interview will be conducted to the eligible candidates, if the large numbers of candidates are found to be eligible in the screening. If the lesser number of candidates are found to be eligible in the screening, interview will be conducted only to the eligible candidates for final selection. If written test is conducted, the names of the shortlisted candidates will be displayed on the Notice Board, which is kept in front of the Conference Hall on the same day.

Note: The applications will not be accepted by post/ courier.


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

Sunday, December 13, 2015

Call for the IPSF Internship at WHO – Famous Pharmacist Study

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IPSF is delighted to introduce you to an internship opportunity at the World Health Organization. Through IPSF, the WHO Unit for Health Promotion will recruit one pharmacy student or recent graduate to work at their main headquarters in Geneva. 


Scope: The internship offered is for a position assisting with the Famous Pharmacist Study, which focuses on the role of the pharmacist, based on review of the work of prominent pharmacists. 

Duration: The length of the internships will be from two to three months. Regarding the terms of internship, flexibility is possible, however the earliest start date is preferred.

Program & Candidate Qualifications : Under the supervision of Dr Kwok-Cho Tang, Coordinator of the Health Promotion and Noncommunicable Diseases and Mental Health department, the intern will execute various tasks in the context of the research project. Based on the nature of the project, the ideal candidate should:
• Possess excellent writing skills
• Have experience in qualitative research methods
• Have completed his or her undergraduate pharmacy study

Depending on the intern’s area of interests and skills, alongside with the approval from the WHO supervisor, IPSF additionally offers an opportunity to:

• Contribute to the IPSF Policy/Public Health Committee as a co-opted member

• Partake in the IPSF delegation to the 57th WHO World Health Assembly.

• Attend conferences and represent IPSF at United Nation meetings in Geneva with either permanent or special ground passes to UN buildings.

Eligibility: WHO may accept applicants who meet all of the following conditions as interns:

• Applicants who are fluent in English

• Applicants must not be related to a WHO staff member (e.g., son/daughter, brother/sister or mother/father)

• Applicants cannot have participated previously in a WHO internship program

• Applicants who are not current tobacco users.

Applications invited for SRF and RA : CSIR -2015

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The Human Resource Development (HRD) Group of Council of Scientific and Industrial Research (CSIR), New Delhi, provides opportunities to bright young men and women in the form of direct Senior Research Fellowships (SRFs) and Research Associateships (RAs) for training in methods of research under the expert guidance of faculty members/scientists working in universities, laboratories and institutes of Government Departments and recognised laboratories of industry in various fields of science and technology.
Preference will be given to the research topics relevant to R&D programmes of CSIR Laboratories, in the new and emerging fields of science and in the areas of importance for development of scientific and technological capability of the country. The Fellowships/ Associateships are tenable in all the universities and deemed universities/IITs/postgraduate colleges/government research establishments including those of CSIR, R&D establishments of recognised public sector, industrial firms and other recognised institutions. Only bonafide Indian citizens are eligible for the award. The award is for fixed tenure and does not imply any assurance or guarantee for subsequent employment by CSIR to the beneficiary. CSIR reserves the right to determine the place in India best suited to provide necessary facilities in the areas of science in which the awardee is to specialize. Selected Fellows and Associates will have to devote their full time to the approved research programmes. Fellows and Associates are not permitted to take up any other remunerative jobs/assignments during their tenure.

A. SENIOR RESEARCH FELLOWSHIPS

ESSENTIAL QUALIFICATIONS:

MSc/BE/B. Tech or equivalent degree with at least 55% marks and one publication in Science Citation Indexed (SCI) Journal and should have completed at least two years of post MSc/BE/B. Tech research experience as on the last date of application, as evidenced from fellowship/ associateship or from date of registration for Ph.D.
OR
MTech/ME or equivalent degree in engineering/technology with at least 60% marks.
OR
BE/B. Tech or equivalent degree with at least 60% marks and two years research experience as on the last date of application.
OR
MBBS/BDS or equivalent with at least 60% marks and one year internship.
OR
BPharm/BVSc/BSc(Ag) or equivalent degree with at least 55% marks and one publication in SCI Journal and should have completed at least three years research experience as on the last date of application, evidenced from fellowship/associateship or from date of registration for Ph.D.
OR

Apply Online on or before 14th December 2015 at http://www.csirhrdg.res.in

Wednesday, November 25, 2015

Walk In Event for Freshers : Approaching soon

Role: Clinical Research Associate/Scientist

Walk in event for the below roles: 

1. Clinical Research Professionals : Candidates with 1 to 8 years of experience in clinical research field. Preferably candidates with site monitoring experience. 

2. Clinical Research Freshers : Looking for candidates with strong clinical background and communication skills who have good domain knowledge.

All roles require excellent communication skills and will involve working in shifts.

Event details: Date : Nov 28th 2015  Registration Timings :  8am to 10am 

Documents to carry - CV, last 3 months pay slip, ID proof

Assessment process - CV screening, Aptitude tests, HR Interview, Technical interview, Final interview 
Job location - Bangalore, Number of openings - Multiple. 

Interview Location:  Quintiles

Etamin Block, Wing A, Ground floor

Prestige Tech Park II, Outer Ring Road

Sarjapur, Bangalore - 560103

Job Description:- Clinical Roles: Apply clinical research expertise to provide project related assistance across complex and multiple project(s), sites and project teams. Lead teams functionally, where assigned, including awareness of scope of work, budget, and resources. Ensure all work is conducted in accordance with SOPs, policies and practices, good clinical practices and applicable regulatory requirements and meets quality and timeline metrics. 

Required Knowledge, Skills and Abilities: Advanced knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Familiarity with related systems and software utilized in clinical operations. Strong written and verbal communication skills including good command of English language. Results and detail-oriented approach to work delivery and output.

Interested Candidates can walk in at the above mentioned venue or send in the resumes to sindoora.kn@quintiles.com
Salary: INR 2,00,000 - 4,00,000 P.A
Desired Candidate Profile :
Education- UG: B.Sc - Any Specialization, BDS - Dentistry, MBBS - Medicine
PG: Any Postgraduate - Any Specialization, Post Graduation Not Required
Doctorate: Any Doctorate - Any Specialization, Doctorate Not Required
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.
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    Regards,
    Deepak Kumar Bandari,
    Pharm.D Intern,
    Vaagdevi College of Pharmacy - India
    Elsevier Student Ambassador - South Asia

Pharmacist required : Cancer Treatment Services Hyderabad Pvt. Ltd.

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Requirements : B.Pharm (1-6 years experience)
Responsible for checking prescriptions to ensure that there are no errors and that they are appropriate and safe for individual patients
- Provides advise on the dosage and the most appropriate form of medication.
- Ensures medicines are stored appropriately and safely
- Responsible for answering the queries of the patients and patient attendants.
- Responsible for rack verification as per the schedule
- Responsible for coordination with stores department for replenishment of drugs
Salary: INR 80,000 - 1,50,000 P.A
Role: Clinical Research Associate/Scientist
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    Regards,
    Deepak Kumar Bandari,
    Pharm.D Intern,
    Vaagdevi College of Pharmacy - India
    Elsevier Student Ambassador - South Asia

Vacancies for Pharmacist : Krishna Institute of Medical Sciences Ltd.

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Role and Responsibilities: 
  • Pharmacist will handle the prescription of the patient.
  • Make the bill according to the prescription
  • Take the medicines according to the prescription
  • Check the medicines according to the prescription
  • Explain the dosage of the drugs

Role: Pharmacist/Chemist/Bio Chemist
Experience : 1-3 years
Location : Hyderabad

Desired Candidate Profile : Education:

UG: Any Graduate - Any Specialization, Graduation Not Required

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

Doctorate: Any Doctorate - Any Specialization, Doctorate Not Required 

Company Profile: Krishna Institute of Medical Sciences Ltd.; Multi Specialty Hospital located centrally, established with international standards, 300 bed, managed by highly qualified Doctors and Health care professionals.

Click Here to Apply

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

Tuesday, November 24, 2015

WHO Internship programme : Applications are invited

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The World Health Organization (WHO) as the leader in global public health issues is committed to building future leaders in public health. WHO's Internship Programme offers a wide range of opportunities for students to gain insight in the technical and administrative programmes of WHO.

Unfortunately, WHO internships are not paid and all costs of travel and accommodation are the responsibility of the intern or the sponsoring institution.

Who are we looking for? 
  • You are enrolled in a degree programme in a graduate school (second university degree or higher) both at the time of application and during the internship.
  • You have completed at least three years of full-time studies at a university or equivalent institution towards the completion of a degree.
  • You are at least 20 years old.
  • You possess a first degree in a public health, medical or social field related to the technical work of WHO or a degree in a management-related or administrative field.
  • Fluent in the working language of the office of assignment.
How can I apply?

To apply, you must submit a completed WHO Personal History Form (PHF) [MS Word 294] along with a duly signed Cover Letter.
The Cover Letter should express your motivation for applying for a WHO Internship (maximum length - three paragraphs), WHO work area of interest and dates of availability.

Applications should be sent to:
Personnel-Recruitment Unit
World Health Organization
Regional Office for South-East Asia
World Health House
Indraprastha Estate
New Delhi-110002, India
Telephone: 011-23370804

Conditions of WHO internships : 
The duration of WHO internships is between a minimum of 6 weeks to a maximum of 12 weeks. Exceptionally, internships may be extended up to 24 weeks to respond to special academic requirements or particular needs of the receiving programme.
  • WHO internships are not paid. Travel costs, travel arrangements (including visas), and living accommodations are the responsibility of the intern or their sponsoring institution.
  • Persons related to a WHO staff member, i.e., son/daughter, brother/sister are not eligible for an internship.
  • WHO Interns must have adequate medical insurance coverage during the entire period of the internships.
  • Interns may participate only once in the WHO Internship Programme.
  • Interns do not have the status of WHO staff members and shall not represent the Organization in any official capacity.
  • WHO Interns are not eligible for appointment to any position within WHO for a period of three months following the end of their internship. Any employment with WHO at that point in time shall be subject to established recruitment and selection procedures.


If you have any questions please do not hesitate to contact us at

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

Monday, November 23, 2015

Applications open for Senior Research Fellowships and Research Associates - 2015 : CSIR

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

Tuesday, November 17, 2015

Overseas Doctoral Fellowship to Indian Students

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Science and Engineering Research Board (SERB), a statutory body under the Department of Science and Technology, Government of India has recently approved the launch of SERB Overseas Doctoral Fellowship. 
  • Under this programme SERB provides fellowship to Indian students graduating from Indian universities/ institutes to pursue Ph.D. in areas of science, technology, engineering and medicine in academic institutions of international repute abroad.
  • The Programme aims to build national capacity where the talent supply of researchers in areas of interest to the country is sub-critical.
  • The applicant should be an Indian and have completed eligible degree in India (Bachelor/Post graduate) in Science or Engineering (including Medicine, Pharma, Agriculture and related S&T areas) not earlier than preceding two years.
  • The applicant should have got admission into doctoral research program in *specified areas in overseas top ranking universities. The fellowship amount will be US $24,000 per annum.
  • The fellowship will be offered for a period of 4 years. In exceptional cases, the fellowship can be extended for one more year.
  • In addition, one time Contingency/Preparatory allowance of Rs. 60,000/- and return Airfare (Economy) will be given to every fellow.
  • SERB is in a process of initiating dialogue with top ranking overseas Universities to explore long term partnerships to build quality human capacity. 
SERB has entered Memorandum of Understanding (MoU) with the following Universities:


SERB has been negotiating with more top ranking Universities. Students who secured admission in other top ranking Universities across the globe can also apply for these fellowships. They should send the applications directly to SERB along with a copy of admission offer letter from the overseas institution and their bio-data. In this case, selected fellows will be provided a fellowship of US $24,000 per annum and one time Contingency/Preparatory allowance of Rs. 60,000/- and return Airfare (Economy). The selected candidate is required to execute a bond on a non-judicial stamp paper of Rs.100/- before a notary-public/Oath of Commissioner as per specimen bond of SERB. The candidates are required to return to India after completion of their Ph.D. However, permission for staying for another four years after completion of the Ph.D course may be considered, for the reasons to be recorded in writing without any financial support of any kind whatsoever from SERB. 


For details, please contact: 
Praveenkumar S Programme Officer, 
Overseas Doctoral & Postdoctoral Fellowship Science and Engineering Research Board 5 & 5A, 
Lower Ground Floor Vasant Square Mall Sector-B, 
Pocket-5 Vasant Kunj New Delhi-110070 
praveen@nic.in 
Phone: (011) 2659 0353 / 0324 (011) 4000 0345; 
Tele.Fax No. (011) 2696 3695

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