Chandigarh

21 February 2014

AWARD OF DBT-JUNIOR RESEARCH FELLOWSHIP (DBT-JRF) IN BIOTECHNOLOGY at National Centre for Cell Science

Applications are invited from Indian nationals for the award of “DBT-Junior Research Fellowship” (DBT-JRF) for pursuing research in frontier areas of Biotechnology and Applied Biology. JRFs will be selected according to merit under two categories: Category I & II. Category I fellowship (Top 275 in number) are tenable in any University/Institute in India where the students can register for Ph.D. Category II students (100 in number) will be eligible to join any DBT sponsored Project and avail fellowship equivalent to NET/GATE qualifications as per DST Guidelines, subject to selection through institutional selection process. Fellowship will be co-terminus with the duration of project and institutional rules will be applicable. There will be no binding on PIs of DBT sponsored projects to select JRF/SRF for their projects from category II list. Selection in Category II will not entitle student for any fellowship from DBT-JRF programme.

Post: Junior Research Fellowship
10 February 2014

4th National Level Workshop on Computer Aided Drug Designing at Pune

RASA Life Science Informatics in collaboration with Padmashree Dr. D. Y. Patil Institute of Pharmaceutical Science and Research

Is organizing the

"4th National Level Workshop on Computer Aided Drug Designing”

7^th March to 9^th March 2014.

7 February 2014

Bioinformatics Institute of India invites admissions for career Boosting Distance Learning & E-learning Programs in Pharma & Life sciences for year 2014- 100 % Job Assistance in industry

3 February 2014

Enrolment Closing for the Professional Training Programs in Clinical Research and Pharmacovigilance (via Distance Learning) at Catalyst Clinical Services Pvt. Ltd.

The enrolment for the Feb’14 batch of Professional Diploma in Clinical Research (PDCR) and Professional Certificate in Pharmacovigilance (PCPV) program is closing on 10-Feb-2014.Please send your Application Form by the due date in order to secure enrolment in Feb’14 batch

These training programs are aimed at imparting knowledge and skills required for clinical research and pharmacovigilance profession thereby enabling the participants to explore a career in these emerging streams. Optimal course fee and ease of training and evaluation has led to the wider acceptability of the programs amongst students and researchers.

Program(s) Highlights		Clinical Research and PV Opportunities
• Optimal Duration : 6 months correspondence program, requires approximately 80 hours of total reading. • Assignment based evaluation, no written examination. • Optimal Course Fee. • Comprise of high quality study modules in line with the requirements of the clinical research and PV Industry. • Wide recognition and acceptance of the program through out the industry making PDCR India's largest CR training program. • Placement guidance provided to successful participants.		• Global Clinical Research (CR) industry is estimated at $52 bn ofwhich CRO marketsize is estimated at$17.8 bn. • More than 2600 clinical trials are being conducted in India across 5000+investigator sites (ctri.nic.in) • The Pharmacovigilance (PV) market worldwide was $1860 million in 2008 & is estimated to reach $2252 million by 2015. • India is the fourth largest producer of pharmaceuticals in the world with more than 6,000 licensed drug manufacturers and over 60,000 branded formulations. • In India more than 150 companies are actively engaged in Clinical Research and Pharmacovigilance field.

Professional Diploma in Clinical Research (PDCR)

Module 1: Introduction to Pharmaceutical Medicine
- New Drug Discovery
- Clinical Development of Drug
- Essential Clinical Trial Documents etc.
Module 2: Good Clinical Practice (GCP) Foundations
- History of GCP - milestones in the evolution of GCP
- Principles of GCP
- Ethics in Clinical Research
- Biostatistics etc.
Module 3: Drug Regulatory Affairs (Clinical Trials)
- Overview of Regulatory Environment in USA, Australia, Europe & India
- Clinical Trial Application Requirements in India
- HIPAA Privacy Rule
- IND/ANDA/New Drug Application etc.
Module 4: Roles & Responsibilities of Clinical Trial Personnel

READ MORE >>>

Professional Certificate in Pharmacovigilance (PCPV)

1. Introduction to Pharmacovigilance (PV) and Risk Management
2. Standard Terms and Definitions
3. Global Perspective of PV and ADR Reporting
4. Guidelines and Standard Governing PV
5. Global AE Reporting System and Reporting Forms
- US FDA Form 3500 and 3500A
- Medicines and Healthcare Products and Regulator Agency's Vigilance Reporting Form-Yellow Card
- Medeffect Canada and Canada Vigilance Program
- Suspected Adverse Drug Reaction Reporting (SADRR) Form
- Universally Accepted ADR Reporting Form CIOMS I Form etc.
6. Individual Case Safety Reports (ICSRs)
7. Medical Dictionary for Drug Regulatory Activities (MedDRA)
8. Periodic Safety Update Reports (PSURs)
9. Expedited Reporting and Requirements
10. PV Inspection and Compliance Monitoring

READ MORE >>>

Jobs & Opportunities after PDCR & PCPV
Loading...

Clinical Research Associate (CRA), Clinical Research Coordinator (CRC), Clinical Data Manager (CDM ), Drug Safety Associate (DSA) etc.

Highlights of PDCR and PCPV Programs:
Ease of Training and Evaluation: Distance learning mode and Assignments based evaluation
Optimal Duration: 6 months
Course Fee: Rs. 9600 each (DD in favour of Catalyst Clinical Services Pvt. Ltd. payable at Delhi)
Last Date of Enrolment: 10th February 2014

Follow the links below to download the Application Form. Our placement assistance can also be viewed on the same link,

<< DOWNLOAD APPLICATION FORM FOR PDCR >>

<< DOWNLOAD APPLICATION FORM FOR PCPV >>

Enrolment Procedure:
In order to enrol, one simply needs to send us the duly filled Application Form (available at the links above), copy of highest qualification certificate and DD of prescribed fee to the address mentioned in the footer of the Application Form.

Advantages of PDCR and PCPV Programs:
- Increases the visibility of your CV
- Equip you with the required knowledge to handle the potential interview questions
- Wide recognition and acceptance of the program(s) throughout the industry
- Placement assistance via regular job postings on CR Network

Contact Details:
Catalyst Clinical Services Pvt. Ltd.
Corporate office:503, NDM-2, Netaji Subhash Place, Pitampura, Delhi – 110034, India
M:+91 9818356273; Ph: +91-11-45121445, 45121435
Email: info@catalystclinicalservices.com

2 February 2014

Applications are invited for Research Assistant from M.S. (Pharm.)/M. Pharm/M.Sc in National Institute of Pharmaceutical Education and Research

The National Institute of Pharmaceutical Education and Research has been established under the aegis of Ministry of Chemicals and Fertilizers, Government of India, Dept. of Pharmaceuticals as a Centre of Excellence in imparting higher education, research and development in pharmaceutical sciences and is the first Institute of its kind in country. The Institute was declared as an Institute of National Importance by Government of India through an Act of Parliament, notified on 26th June 1998. The Institute is a member of the Association of Indian Universities and Association of Commonwealth Universities.

Post: Research Assistant
1 February 2014

Vacancies for Pharmacists (335 Openings) in National Health Mission - Department of Health & Family Welfare

A Healthy Community in a Society determines overall progress of the State. Department of Health & Family Welfare is committed to provide preventive, promotive and curative quality health Services at an affordable price to the people of the state. For this, a wide network of Health Institution consisting of hospitals, Community Health Centres, Primary Health Centres and Subsidiary Health Centres/ Dispensaries to cater to the health needs of the rural and urban population through well trained medical and paramedical staff have been established in the State.

Post: Pharmacists [UH- 77; RBSK - 258]
15 January 2014

Franco-Indian Pharmaceuticals requires Area Sales Manager, Trainee Medical Representative

Franco-Indian Pharmaceuticals Pvt. Ltd., a name that stands for quality and innovation, is one of the major players in the Pharmaceutical Industry in India.
Our innovative, value added products improve the quality of life of people and ease their sufferings and help them to enjoy, longer, healthier and more productive lives.
Franco-Indian’s strongest attributes are the unwavering focus on ethics, transparency, corporate culture, quality of products, contribution to society and commitment to growth.

Post: Area Sales Manager, Trainee Medical Representative
2 January 2014

Applications are invited for Project Assistant Level-II in PGIMER - master degree in Pharmacology/Life-Sciences

The PGIMER owes its inception to the vision of late Sardar Partap Singh Kairon, the then Chief Minister of Punjab and the distinguished medical educationists of the then combined state of Punjab, supported by the first Prime Minister of India Pt. Jawahar Lal Nehru who considered the institutions of scientific knowledge as temples of learning and the places of pilgrimage. The institute started in 1962 and Pt Jawahar Lal Nehru inaugurated the hospital now named “Nehru Hospital” on 7th July 1963. The Institute was originally under the Government of undivided Punjab. After the reorganization of the state, the administrative control of the institute passed on to the Union Territory of Chandigarh in November 1966. The Institute became an autonomous body under the Act of Parliament in 1967 functioning under the Ministry of Health and Family Welfare, Government of India.
9 December 2013

Vacancies for M.Pharm, Masters in Life- sciences as Junior Research Fellow, Senior Research Fellow in PGIMER - 2 posts

The PGIMER owes its inception to the vision of late Sardar Partap Singh Kairon, the then Chief Minister of Punjab and the distinguished medical educationists of the then combined state of Punjab, supported by the first Prime Minister of India Pt. Jawahar Lal Nehru who considered the institutions of scientific knowledge as temples of learning and the places of pilgrimage. The institute started in 1962 and Pt Jawahar Lal Nehru inaugurated the hospital now named “Nehru Hospital” on 7th July 1963. The Institute was originally under the Government of undivided Punjab. After the reorganization of the state, the administrative control of the institute passed on to the Union Territory of Chandigarh in November 1966. The Institute became an autonomous body under the Act of Parliament in 1967 functioning under the Ministry of Health and Family Welfare, Government of India.

Post: Junior Research Fellow, Senior Research Fellow
9 December 2013

Opportunity for Laboratory Assistant @ Ministry of Health & Family Welfare CDSCO

Central Drugs Standard Control Organization, Under the Drug and Cosmetics Act, the regulation of manufacture, sale and distribution of Drugs is primarily the concern of the State authorities while the Central Authorities are responsible for approval of New Drugs, Clinical Trials in the country, laying down the standards for Drugs, control over the quality of imported Drugs, coordination of the activities of State Drug Control Organisations and providing expert advice with a view of bring about the uniformity in the enforcement of the Drugs and Cosmetics Act.

For the post of Laboratory Assistant Eligible & Interested candidates may submit their applications direct to Director Regional Drugs Testing Laboratory, Chandigarh

Post: Laboratory Assistant