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Online training on pharmacovigilance for freshers


77 replies [Last post]
Anonymous

Hello Guys,

Good news for freshers,

We are provide the online training on Pharmacovigilance.We will provide online axis for the database which is very demand in present market. I feel this is a very good opportunity to all of you to expose yourself some practical and theoretical session.

Following are the details of the softwares which you are going to be trained.

Software: World Top leading database,

               Eudravigilance

Qualifications: MSc life sciences,M.Pharma,B.Pharma,MBBS,BDS,BVMS or any related Life sciences degree. 

Direct online axis on the safety database.

Note:This is not PV institute.so Pls dont think commercially

If any one have interested Pls contact me at 09810691948 or naren.bt6@gmail.com

 

Thanks,

Naren,

09810691948,

naren.bt6@gmail.com


naresh111
Offline
Joined: 2012-04-10
please contact to 08123615219 for Pharmacovigilance trainings

Hi,
Pharmacovigilance trainings still available. Please contact to me at 91-8123615219 or naren.bt6@gmail.com.

biomedinfo's picture
biomedinfo
Offline
Joined: 2011-08-25
Online Pharmacovigilance Training in Oracle Argus Safety

Online Pharmacovigilance Training in Oracle Argus Safety Database with Project @ BioMed Informatics Medwin Hospitals

 
BioMed Informatics Medwin Hospitals is a leading Clinical Research Organization offering full range of Clinical Research, Clinical Data Management, Oracle Clinical OC/RDC, Pharmacovigilance, Oracle Argus Safety, SAS Clinical, IPR & Regulatory Affairs trainings since the year of 2000 that are helpful for Life Sciences/Pharmacy students to enter into IT Companies and Pharma, Biotech, CRO industries.
 
Oracle Argus Safety is an advanced and comprehensive adverse events (AE) management system that helps life sciences companies enable regulatory compliance, drive product stewardship, and integrate safety and risk management into one comprehensive platform. Argus Safety is industry-proven and accepted, having been used for more than a decade at leading Pharmaceutical, Biotech, CRO, and IT Companies. Trainees get hands on practical training experience to create career paths.
 
Mode of Training:Instructor Led Class room/Online Training
 
Online TrainingFeatures:
Ø  Web based classroom
Ø  One faculty/student
Ø  Placement support
Ø  Regular/Fast track/Weekend batches
Ø  Flexible timings 
Ø  Training Mode: Skype/Teamviewer
Ø  Hands-On Training on the Database
Ø  Direct access to Oracle Argus Safety Database
 
Our candidates employed in Novartis, Quintiles, TCS,Parexel International (India) Pvt Ltd, MakroCare, Global Hospitals, Apollo Hospitals, NIMS, Glenmark Pharmaceuticals Ltd, Jubilant, Reliance Life Sciences, Shantha Biotechnics Ltd, Mahindra Satyam, SMO Clinical Research (I) Pvt Ltd, Pioneer Corporate Services Inc-USA, ICMR, AstraZeneca-UK, Texas Woman’s University-USA and many more…


Certification
Certificate will be provided for this course on successful completion of Assignments & Projects. Certificate would be awarded at the end of the program by BioMed Informatics Medwin Hospitals.

Interested candidates are kindly requested to fill the enquiry form in the website www.biomedlifesciences.com for further information.

Please note that we also provide separate hostel facility assistance for ladies as well as gents. 
 
Contact:
 
G.V.L.P. Subba Rao
BioMed Informatics
Medwin Hospitals B Block First Floor,
Nampally, Hyderabad-500 001, India
Phone: 040 - 40209750
Website: www.biomedlifesciences.com
 
Course Curriculum:
·         Clinical Development process
·         Different phases of Clinical Trials
·         History and overview of Pharmacovigilance
·         Introduction and responsibilities of USFDA, EMA and CDSCO
·         Pharmacovigilance in India
·         Adverse Events and its types
·         Drug Safety in clinical trials and post marketed drugs
·         Different sources of Adverse Events reporting
·         Different types of AE Reporting Forms
·         Expedited reporting and its timelines
·         Different departments working on Pharmacovigilance
·         Roles and responsibilities of case receipt unit
·         Roles and responsibilities of Triage unit
·         Four factors for the reportable case
·         Seriousness criteria of adverse event
·         Expectedness or Listedness of adverse event
·         Causality assessment of the adverse event
·         Importance and procedure of duplicate check
·         Data Entry
·         Case booking or initiation
·         Case processing
·         MedDRA and WHODD coding
·         SAE narrative writing
·         Case quality check, Medical review and its submission
·         PSUR and its submission timelines
Practical Hands-on Training on Oracle Argus Safety Database
Argus Console:
·         PV Overview
·         PV Business process
·         Introduction to Oracle Argus Safety Database
·         Family, Product and License creation
·         Study creation
·         Sites, users and Groups creation
·         Workflow Configuration
·         Expedited Report Configuration
·         Case priority Configuration
·         Case Numbering
·         Field Validation
·         Code list Configuration
·         LAM (Local Affiliate Module) Configuration
Argus Safety:
·         Different icons used during the case processing and their purpose.
·         Different tabs used in case processing
·         Minimum requirements for a case bookin
·         Case Bookin and Data entry
·         Case Processing
·         Case Routing Based on workflow
·         Case Quality check, Medical review
·         Duplicate case check or verification
·         Report Generation for Regulatory Submission
·         Expedited Reports and Aggregate Reports
·         Case Bookin in LAM and Routing to Central Safety database
·         MedDRA coding and WHO DD coding
·        Narrative Writing
·         Different Case Studies
You will be extensively involved in:
·         Data entry of Individual Case Safety Reports (ICSRs) in to the Argus Safety database
·         Processing of all incoming cases in order to meet timelines
·         Writing a detailed medically oriented description of the events in the form of safety narrative.
·         Perform the duplicate search in Argus safety database
·         Assessment of seriousness, expectedness/listedness of Adverse Events
·         Evaluate the entered cases as per quality review checklist in terms of quality, accuracy, and completeness against the source documents provided
·         Performing QC review of the cases to meet case processing timelines
·         Coding of adverse events with the help of MedDRA and labeling the events
·         Coding of suspect and concomitant drugs using company and WHO-DRUG dictionaries.
·         Meeting the timelines and supporting global regulatory submissions in expedited reporting of ICSRs
·         Preparation of PSURs for regulatory submissions
·         Entry of Adverse events in Local Affiliate Module (LAM) and Routing Local events to central Argus safety
·         Codelist Configuration in Argus console
·         Creating Sites, Users, User groups
·         Creating Products, Licenses, Studies and Expedited Reporting Rules
·         Configuring Workflow States and rules
·         Knowledge of Advanced conditions; Setting up of field validation to ensure consistency of data

naresh111
Offline
Joined: 2012-04-10
contact to 08123615219 for free Pharmacovigilance trainings

Hi,
If any one interested please contact to to 8123615219 for Pharmacovigilance trainings.
Regards,
naresh.

naresh111
Offline
Joined: 2012-04-10
Online training on pharmacovigilance for freshers

still free online trainings available on Pharmacovigilance.contact to below no
updated no:08123615219
Regards,
naren.

naresh111
Offline
Joined: 2012-04-10
Urgent openings for Clinical research associate

Urgent Openings; Position: Clinical Research Associate (Central Monitor), Location: Hyderabad, Requirements: Should have at least 4-5 years of clinical research and minimum 2 years of eCRF monitoring experience in reputed organization. Kindly submit your CV to skumar2@rpsweb.com and tjiang@rpsweb.com. Please share this with your connections to reach all clinical research professional interested in these openings.

naresh111
Offline
Joined: 2012-04-10
DRUG SAFETY ASSOCIATE in ICON RESEARCH

DRUG SAFETY ASSOCIATE in ICON RESEARCH

Education: Medical/science background (nursing preferred) and/or bachelor’s degree or local equivalent.
Experience:
The successful candidate will have appropriate clinical research/pharmaceutical industry experience, ideally in pharmacovigilance/drug safety, with understanding of medical terminology and coding systems.Must be proficient in written and verbal English with excellent communication skills and fundamental computer skills.

Job location: Chennai

to apply online click below mentioned website then select job location(india)>click search button>Now you can see list of jobs ,Click on DSA

Anonymous
Urgent openings for Clinical research associate

Urgent Openings; Position: Clinical Research Associate (Central Monitor), Location: Hyderabad, Requirements: Should have at least 4-5 years of clinical research and minimum 2 years of eCRF monitoring experience in reputed organization. Kindly submit your CV to skumar2@rpsweb.com and tjiang@rpsweb.com. Please share this with your connections to reach all clinical research professional interested in these openings.

biomedinfo's picture
biomedinfo
Offline
Joined: 2011-08-25
Pharmacovigilance Training in Argus Safety Database

BioMed Informatics Medwin Hospitals providing job oriented Pharmacovigilance training programme in Argus Safety Database.
 
Thanks
GVLP.Subba Rao
www.biomedlifesciences.com

Anonymous
fee structure and course duration

respected sir,
kindly tell me the duration of PG DIPLOMA course n fees structure
thanx
my email id is
vish.cherry@yahoo.com

biomedinfo's picture
biomedinfo
Offline
Joined: 2011-08-25
Pharmacovigilance Training in Oracle Argus Safety Database

BioMed Informatics Medwin Hospitals (Member of BCIL-DBT) is a leading Clinical Research organization offering full range of Clinical Research, Clinical Data Management, Oracle Clinical OC/RDC, Pharmacovigilance, Oracle Argus Safety & SAS Clinical training services to Healthcare Organizations globally since the year of 2000.
 
The classes will be conducted at BioMed Informatics Medwin Hospitals, Hyderabad.
 
Oracle Argus Safety is an advanced and comprehensive adverse events (AE) management system that helps life sciences companies enable regulatory compliance, drive product stewardship, and integrate safety and risk management into one comprehensive platform. Argus Safety is industry-proven and accepted, having been used for more than a decade at leading Pharmaceutical, Biotech, CRO, and IT Companies. Trainees get hands on practical training experience to create career paths.
 
The focus of the Pharmacovigilance training in Oracle Argus Safety mainly includes the following topics:
·         Clinical Development process
·         Different phases of Clinical Trials
·         History and overview of Pharmacovigilance
·         Introduction and responsibilities of USFDA, EMA and CDSCO
·         Pharmacovigilance in India
·         Adverse Events and its types
·         Drug Safety in clinical trials and post marketed drugs
·         Different sources of Adverse Events reporting
·         Different types of AE Reporting Forms
·         Expedited reporting and its timelines
·         Different departments working on Pharmacovigilance
·         Roles and responsibilities of case receipt unit
·         Roles and responsibilities of Triage unit
·         Four factors for the reportable case
·         Seriousness criteria of adverse event
·         Expectedness or Listedness of adverse event
·         Causality assessment of the adverse event
·         Importance and procedure of duplicate check
·         Data Entry
·         Case booking or initiation
·         Case processing
·         MedDRA and WHODD coding
·         SAE narrative writing
·         Case quality check, Medical review and its submission
·         PSUR and its submission timelines
 
Mode of Training:Instructor Led Class room/Online Training
 
Online TrainingFeatures:
Ø  Web based classroom
Ø  One faculty/student
Ø  Placement support
Ø  Regular/Fast track/Weekend batches
Ø  Flexible timings 
Ø  Training Mode: Skype/Teamviewer

Our candidates employed in Novartis, Quintiles, Parexel International (India) Pvt Ltd, MakroCare, Global Hospitals, Apollo Hospitals, NIMS, Glenmark Pharmaceuticals Ltd, Jubilant, Reliance Life Sciences, Shantha Biotechnics Ltd, Mahindra Satyam, SMO Clinical Research (I) Pvt Ltd, Pioneer Corporate Services Inc-USA, ICMR, AstraZeneca-UK, Texas Woman’s University-USA and many more…
 
Certification
Certificate will be provided for this course on successful completion of Assignments & Projects. Certificate would be awarded at the end of the program by BioMed Informatics Medwin Hospitals.
 
Interested candidates are kindly requested to fill the enquiry form in the website www.biomedlifesciences.com for further information.
 
Please note that we also provide separate hostel facility assistance for ladies as well as gents. 
 
Contact:
G.V.L.P. Subba Rao
BioMed Informatics
Medwin Hospitals B Block First Floor,
Nampally, Hyderabad-500 001, India
Phone: 040 - 40209750
Website: www.biomedlifesciences.com

naresh111
Offline
Joined: 2012-04-10
openings for freshers

Freshers Aiming for "Medical Writer F3" Domain Apply @ Spirant Communication Pvt Ltd
Job Description:

Ensure timely production of high quality documents (manuscripts, abstracts, short communications, review articles) for publications and preparing communication material supporting pharmaceutical brands.
Candidate should have flawless english writing skills
Excellent communication and presentation skills
Literature reviewing and evaluation capabilities
Clear, concise scientific style of writing

Experience: 0 - 3 Years

Qualification: B.Pharm/M Pharm Pharmacy

How to Apply: Send your application to careers@spirant.org

Anonymous
B.pharma

I am serching for good job

naresh111
Offline
Joined: 2012-04-10
Openings for B Pharmacy and M pharmacy for Pharmacovigillance

Openings for B Pharmacy and M pharmacy for Pharmacovigillance. Day: August 17, 2013. at Accenture on 17th august for PV .Venue: Aceenture, Near HSBC , Bannergatta road, Arekere. Bangalore.Referral Id: Sathish kumar.P Emp Id :10764545 sathishkumar.pp@accenture.com Registration Time: 10:00 am to 12:00pm

Anonymous
openings for freshers

Freshers Aiming for "Medical Writer F3" Domain Apply @ Spirant Communication Pvt Ltd
Job Description:

Ensure timely production of high quality documents (manuscripts, abstracts, short communications, review articles) for publications and preparing communication material supporting pharmaceutical brands.
Candidate should have flawless english writing skills
Excellent communication and presentation skills
Literature reviewing and evaluation capabilities
Clear, concise scientific style of writing

Experience: 0 - 3 Years

Qualification: B.Pharm/M Pharm Pharmacy

How to Apply: Send your application to careers@spirant.org

naresh111
Offline
Joined: 2012-04-10
Lot of openings released

Job Alert 07 Aug. 2013

1-Apprentice by PIRAMAL ENTERPRISES LTD in Mumbai
Experience: 0 to 1 yrs. | Salary: INR Less Than 50,000 - 1,50,000 P.A | Opening(s): 1
More info click here....www.pharmanews.pharmamedix.in

2-Urgent Requirement - Medical Representative(pharmaceuticalsSales Job)
by Cadila Pharmaceuticals Limited in Ahmedabad, Mumbai, Bengaluru/Bangalore
Experience: 0 to 1 yrs. 
More info click here.... www.pharmanews.pharmamedix.in

3-Hospital Pharmacist
by TOSH Hospitals in Chennai
Experience: 0 to 2 yrs. 
More info click here.... www.pharmanews.pharmamedix.in

4-Territory Business Manager
by Winners Consultancy Services hiring for A leading Pharma MNC in Kolkata, Malda , Midnapur
Experience: 0 to 2 yrs. | Salary: INR 1,50,000 - 2,50,000 P.A | Opening(s): 3
More info click here.... www.pharmanews.pharmamedix.in

5-Medical Representative Pharma, Udaypur Dungarpur Kota
by L.K Saddi Associates hiring for A client of L K Saddi Associates, Associates of a well known Pharma Company in Kota, Udaipur
Experience: 0 to 4 yrs. | Salary: INR Less Than 50,000 - 1,75,000 P.A
More info click here.... www.pharmanews.pharmamedix.in

6-Executive-purchase
by Pharmaffiliates Analytics Synthetics P Ltd in Chandigarh, Panchkula
Experience: 0 to 1 yrs. 
More info click here.... www.pharmanews.pharmamedix.in

7-Patent Research-biotech,biomed,food Technology,pharma
by Evalueserve.com Pvt. Ltd in Gurgaon
Experience: 0 to 3 yrs. | Salary: INR 3,25,000 - 7,00,000 P.A | Opening(s): 4
More info click here.... www.pharmanews.pharmamedix.in

 

 
 

Anonymous
***Pharmacovigilance boot camp*** ICON

***Pharmacovigilance boot camp*** ICON is conducting FRESHERS (only life science graduates like Mpharma, Bpharma, Btech Biotech, Msc lifescience) drive in coming few days. Please do send your resume to nilamadhab.mahapatra@iconplc.com to get schedule.

naresh111
Offline
Joined: 2012-04-10
Urgent Openings -Clinical Research Associates

Urgent Openings -Clinical Research Associates: Location Hyderabad: Candidates with minimum 3-5 years in clinical research and minimum 1-2 year of eCRF monitoring experience. Interested candidates can forward CV to skumar2@rpsweb.com.
Thank you

Anonymous
walk-ins for the post of scientific medical writer in Indegene

gud news for job seekers who hav been completed masters in any dept for freshers

direct walk-ins for the post of scientific medical writer in Indegene life sciences
salary offered :3laks/annum
experience :only freshers
bond upon selection : 1 year must (even for girls too)
qualification:only mpharm any specialisation
job role : documentation work on system

date of walk-in :jun-1(saturday)
time :9am onwords
address : manyatha embassy bussiness park
3floor,ASPEN block G4,nagawara
outer ring road
banglore-560045

note : carry ur update resume soft copy with passport photos

Anonymous
Hello Guys, i am freshers,of

Hello Guys,

i am freshers,of b.pharma student, plz tell me about this detail online training on Pharmacovigilance
my E-MAIL I.D:-DS30154@GMAIL.COM

Thanks

Anonymous
pharmacovigilance

hi,
I am in 2nd year of m.pharm (pharmaceutical chemistry). Can you give me information about Pharmacovigilance, its scope and placement?

Thank you!
my email address- zaidipharma29@gmail.com

Anonymous
online training of pharmacovigilance program

hello sir,

I have completed my M. pharmacy in DRA. Now i want to enter in CRO And pharmacovigilance field. So, I want to join online pharmacovigilance Training program.

Please tell me about this online program send me detail of this on my mail-id -- vinodpharma09@gmail.com .

thanks

Anonymous
openings in Bangalore

HI All,

There are openings at Quintiles, Bangalore for the Position:
1. InForm Programmer
2. SAS Programmer
3. RAVE Programmer
4. OC Programmer

Experience: 1-7 years

Those who are interested, please send your updated CV to vismay.prajapati86@gmail.com

Please mention your experience and post apply for in subject line.

Thanks

Anonymous
Regarding placement and fee.....

Sir, can u tel me regarding pharmacovigilence, scope nd placement.....and also about the how to join and requirement.....

Anonymous
Information of pharmacovigilance

Sir,
I want the information of applying procedure, fee and other information of pharmacovigilance.

naresh111
Offline
Joined: 2012-04-10
Vacancies for CRC in Noida

Vacancies for CRC in Noida.
Clinical Research Coordinator position - interested!!! - send cv to shivuindia@yahoo.com - Place of working - Noida

Anonymous
openings for freshers

Opening for Clinical Data Coordinator freshers in Pune, Mumbai by CR Bridge Placement Solution Pvt. Ltd

Walkin Interview from 28th January to 16th February from 10 AM..

Applicants need to go to the venue mentioned or call on the number provided below

Desired Candidate Profile
Education:(UG - B.Sc - Bio-Chemistry, Biology, Botany, Chemistry, Microbiology, Statistics, B.Tech/B.E. - Bio-Chemistry/Bio-Technology, Biomedical, B.Pharma - Pharmacy) OR (PG - Post Graduation Not Required) OR ( Doctorate - Doctorate Not Required)

Only FRESHERS are ELIGIBLE to APPLY.
WALK-IN Between 10.00 AM to 06.00 PM
Monday To Friday

CR Bridge Placement Solution Pvt. Ltd
9th Floor,
Pride Parmar Galaxy,
Sadhu Vaswani Chowk,
Camp,
Pune-411001

Anonymous
Dear sir,

Dear sir, i am naresh..cmpltd b pharmacy i want information about the pharmacovicelnc plz send details to my id naresh.s828@gmail.com

naresh111
Offline
Joined: 2012-04-10
Trainee Coders

One of our reputed client 'Omega Healthcare Management Services Pvt Ltd.' looking for Trainee Coders. The details are given for your perusal.

Job Title: 
Years of Experience : 0 to 0.6yrs
Type of Employment : Permanent 
Job Location : Bangalore
URL: www. OmegaHealthcareManagementServices.

Job Description

Minimum Experience required: Fresher from Science back ground

CTC: Rs 6500/- per month (Training period)

After training Rs. 11500/- per month

Thanks & Regards
Akram
Inspiration manpower consultancy

Interested candidates can send their resume to akram@inspirationmanpower.co.in or call Akram on + 91 9686454292

Anonymous
Clinical Research Coordinator openings

Urgent requirement of Clinical Research Coordinator for hospital (Fresher also can apply).
Location: Ahmedabad
Kindly forward CV to diacareresearch@gmail.com or talaviyapraful@gmail.com

Anonymous
CRC

Dear sir/Mam

GOOD evening!

I am Rajkishor,looking for a job in clinical research field as a CRC in your organization.I Completed the PGDCR from bangalore.

naresh111
Offline
Joined: 2012-04-10
Associate Research Analyst openings

Jobs at Thomson Reuters, chennai (Monday, 18th February 2013 (Walk In)

Associate Research Analyst:

Require Freshers in B.Pharm, M.Sc Biochemistry, M.Sc Advanced Biochemistry, M.Sc Biotechnology, M.Sc Microbiology, M.Sc Molecular Biology, M.Sc Bioinformatics, M.Sc Genetics or B.Tech Biotechnology. The role would involve review of scientific publications and identify data related to biomarkers, uses of biomarkers in different diseases, identifying the techniques used and enter data into the BMK db using controlled vocabulary and defined data fields.

Date – Monday, 18th February 2013
Time – 4:30 PM - 5:30 PM
Venue – No. 148, Dr. Radhakrishnan Salai, Acropolis, (10th Floor), (Next to Savera hotel), Mylapore, Chennai – 4
Contact Person – Selvakumaran Balraj

Keep smiling,
Naresh

Anonymous
queiry

may i know from which university you are providing this course.if so plz mention whether it had got approval from concerned authorities,fee structure and training tenure and duration.a brother

manusaktteva
Offline
Joined: 2012-10-07
Really Good.

I am surprised that anyone is ready to help and search for it.
Definately I will contact you in couple of time.
But I am confused about location where you will conduct training.

Anonymous
LC-MS/MS Operator

Hello Friends
I am Amit Chapala, i have 4 years experience of handling LC-MS/MS. Working in one of the reputed CRO. Now i want to go for another CRO. If you guys or any recuiter are found any matching jobs please do informe me on amitkchapala@gmail.com.

Anonymous
regarding online pharmacovigilance training programme

dear sir,
i have completed my m.pharmacy this year and i want to
know the details of this training programme. my mail id is sravani.bejjinki@gmail.com

naresh111
Offline
Joined: 2012-04-10
vacancy in Parexel

Hi,

There is an vacancy in PAREXEL International Ltd for the post of Clinical Data Analyst-II.

Please go through the details below:

Description:
Key Accountabilities
¿ Assume the ability to meet the requirements of a CDA I with a high degree of proficiency and autonomy
¿ Take responsibility for specific tasks on projects, or acts as the main CDA contact on individual projects
¿ Train team members on selected tasks
¿ Prepare Data Cleaning Specification 
¿ Review the Data Validation Specification prepared by the Technical Analyst in GTS
¿ Develop or provide input to project specific guidelines, e.g. SAE handling.
¿ Initiate the running of study specific programs 
¿ Utilize current study documentation including protocol, Case Report Forms (CRFs), Cleaning guidelines etc.
¿ Conduct in-house data review, 
¿ Generate and close queries or apply self evident corrections to the data according to the relevant guidelines
¿ Identify and report protocol violations
¿ Manual and Patient Profile review, issue queries
¿ Conduct reconciliation of SAEs, send out queries as required and notify relevant Safety Groups of possible issues for their action
¿ Track and integrate queries
¿ Perform clinical coding if appropriate to role within the project team
¿ If required liaise with 3rd party vendors to clean electronic data
¿ Ensure all documents coded for submission to central files
¿ Lock site(s) within EDC system - remove user's data modification privileges
¿ Interact with site (via mail) as required
¿ Perform early and final database QC activities
¿ Update all relevant tracking system on an ongoing basis
¿ Inform responsible CDA Coordinator of work status regularly
¿ Keep Manager informed about work progress and any issues to avoid surprises. Requires some interaction / supervision by Manager or assigned mentor

Skills
¿ Good computer skills including but not limited to the knowledge of Clinical Trial/Data Management Systems, PMED, knowledge of MS-Office products such as Excel, Word
¿ Sound awareness of all relevant regulations, including GCP
¿ Ability to successfully work in a (`virtual¿) team environment
¿ Client focused approach to work
¿ If required, knowledge of medical terminology and awareness of coding dictionaries (e.g. MedDRA & WHODRUG)
¿ Effectively applies knowledge to provide advice or solutions based on expertise
¿ Offers support and constructive feedback to project team members
¿ Seeks opportunities to develop experience and knowledge
¿ Ability to organize and plan tasks
¿ Excellent interpersonal, verbal and written communication skills
¿ Must be able to work independently but seek guidance when necessary, escalating issues as required
¿ Sense of urgency in completing assigned tasks
¿ Meticulous attention to detail
¿ Effective time management in order to meet daily metrics or team objectives
¿ Shows commitment to and performs consistently high quality work
¿ Willing and able to travel as required ¿ local or international

Experience:
2 to 4 years

If interested, then please send your resume to me at prannoypalkhe@gmail.com.

Do remember,we need experienced people (2 to 4yrs), freshers no need to send resume.

Anonymous
Principle

Pharmaco vigilance principle

Anonymous
Tech Mania Solutions

Greetings From Tech Mania Solutions,

Dear candidate,

We Have Urgent Requirement for Pharmacist for Reputed Pharma distributor Company in hyderabad.

Candidate Must have Pharmacist Certificate

Candidate Must have good communication skills

Qualification: B.pharma or M.Pharma wih Pharmacist certification

Exp:0-2 yrs

Sal:8-14k

Intrested candidate can send there resume to gajula.hr@gmail.com

Regards,

Sudhakar.G

+91-7569649640

Anonymous
seeking information

hello sir iam dinesh.completed BPharm,intrested to know about ur online vogilence programe.my email adr:dinu947@gmail.com

Anonymous
Walk-in for PV@Cognizant

Dear colleagues, Walk-in for PV@Cognizant on 21-Sep-2012: Voice process for freshers, Airoli Navimumbai, mail me your CV@ sourav.chakraborty2@cognizant.com( Source: LinkedIn)

Anonymous
Clinical Research Associate

Job Description:
Position :- Clinical Research Associate
Experience:- 1 to 5 Years in Monitoring
Location :-
1. Delhi - 2
2. Vadodara
3. Pune
4. Nagpur
5. Vizag / Hyderabad
6. Mangalore
Job Post: CRA, Clinical Research Associate, Clinical Monitoring
Company : Siro Pharma ,
Exp: 1- 5Years.

Please see siro pharma website.....

Anonymous
Looking for assistant Manager

Looking for assistant Manager - Drug safety with Experience in RISK Management Plan for Bangalore / India. revert across naresh@nefehr.com

Anonymous
vacancy for clinical research associates

Looking for Clinical Research Associates (2-4 years experience) from M.Pharma background.Excellent organizational skills and ability to manage time and work independently. Excellent written and verbal communications skills. Candidate should know end to end clinical research activities. Please send your profiles to me. Subramanyam.k@makrogrp.com.(Source: LinkedIn)

--

Naresh.

naresh111
Offline
Joined: 2012-04-10
pv walkin at accenture chennai on 6th,7th n 8th of dis month.

 
Hi,
‎2-7 yrs exp required.only intrstd candidates who r willing to attend walkin can send cv to keshava.rao@accenture.com
--
Naresh

naresh111
Offline
Joined: 2012-04-10
job openings in thomson reuters for freshers

job openings in thomson reuters as reasearch Associate for M.Pharm, B.Pharm freshers in hyderabad,
date of interview 6th sep
venue Thomson Reuters – 14th Floor, Cafeteria, Building No. 11, Rajeha Mindspace, Madhapur, Hyderabad
--
Naresh

naresh111
Offline
Joined: 2012-04-10
vacancy for Assistant Manager - Operation Management in Appllo

Assistant Manager - Operation Management 
For Apollo life in Bengaluru/Bangalore, Delhi
Experience: 1 to 5 yrs. Salary: INR 2,25,000 - 3,25,000 P.A. Negotiable Opening(s): 3 
Qualification:MBA(Healthcare)(only)
Responsibilities:

Assisting & Coordinating with OHC (Occupational Health center) staff members.
He/ She will also work to ensure that an adequate number of staff members are available for a particular shift.
Preparation & Coordination for Invoices.
Help in Hiring & Training of OHC Staff.
Ensure smooth funtioning of Occupational Health centers.
Maintaining Good Client relations.
Manage and monitor health programs.
Responsible for OHC dept administrative activities
Forecast of Nursing Staff.

Send your updated resume to career@apollolife.com

Contact Details:
Recruiter Name:Ms.Sowmya
Contact Company:Apollo life
Address: 5th Floor, Life Science Building, Apollo Health Ci Jubilee Hills Jubilee Hills HYDERABAD,Andhra Pradesh,India 500033
Email Address:
Telephone:91-40-23553450
 
 

Anonymous
hi this is kiran

hi i have completed b.sc biotechnology and d.pharmacy and i have 1 year experience as a medical rep am i eligible for this course and what is pharmacovigilance involving in work and is this related to clinical research associate medical coding like programs

kirankylash@gmail.comhttp://www.google.com/recaptcha/api/image?c=03AHJ_Vuv0o23xY7caTFtiSnzvi9kVn-kK9guJRwunfeN8m0S5Mu902hwQkN6CfhdcEzcPqpCZowdXuUvYHXZZh7B5UXm_GpScAKJg-UILI-Zbq_PLkZRs-wdDMDWnNoSbeF4kKnLZ750mvab-Ncm3-VWzTfkj4aFhdbmAKpHrJ3dqkdN1XPHN

Anonymous
Pharmacovigilance training

hi,
Iam Rajesh, I have completed B.Pharmacy and right now pursuing M.Pharmacy. Am i eligible for this course.
If yes please let me know how the teaching mode will be, and when will the course start.
My email id is rajesh_kadavath@yahoo.com

naresh111
Offline
Joined: 2012-04-10
opening for product executive for a pharma company in bangalore

opening for product executive for a pharma company in bangalore.

Roles & Responsibilities:-

1) Strategy Planning for the movement of products

2) Collecting scientific information for literature's
3) Able to explain about Product composition & its usage to the sales team
4) Planning for the promotional activities

Qualification & requirement:-

1) B.Pharma/M.Pharma 
2) Fresher or Min. Exp. of 0.6 yrs as Medical Representative
3) Should be Interested in Marketing
4) Should have sound knowledge on Compositions/Molecules

intrested and eligible candidates forward your resume to 
simhala priyanka
psimhala@finitionsolutions.com

--

Naresh.

naresh111
Offline
Joined: 2012-04-10
Openings for medical affairs at Hetero group of Pharma

Still searching for GROUP HEAD-MEDICAL AFFAIRS at Hetero Group of Pharma companies, with at least 2 years experience each in medical monitoring in clinical trials & medical review function in pharmacovigilance (case processing, aggregate safety reports, RMPs) with ability to handle global teams. Qualification-M.D(Pharmacology), M.B.B.S definitely required (M.B.B.S candidates will need more experience). South zone candidates preferred. 
Interested & eligible (as per above specifications) Please write ASAP to alqhyd@gmail.com.

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