Some important Tips for Writing your CV & Sample format for Pharmacovigilance Job Application "D"

Writing Your CV

Your CV should contain all of the key information pertinent to your job application and someone skim-reading your CV should be able to see all of the key information withina maximum of 20 seconds.  It should fit into 2 or 3 pages at most, be articulate and to the point (no waffling). We recommend that your CV should be simply and clearly set out, ie no tables, on plain paper, bullet pointed and in Microsoft Word. Avoid using photographs, graphics and logos.
 

All CVs should include the following information and ideally in the following order;

Name. Keep this clearly marked at the top of the CV.

Contact details. Make sure you can be contacted easily so put all of your contact details (preferably including an email address and mobile phone number) on the front page.

Nationality. You should also state your eligibility to work if you are not a British Citizen and type of Visa.

Profile. A brief summary about you and your abilities.

Employment history If you work on the agency side you might list examples of clients you have worked with. If you work on the clientside you could list which brands you worked on instead.

Key achievements and responsibilities should be included on your CV. Listing every single responsibility will not interest the reader and will reduce the impact of the CV. Remember your CV is an introduction, the interview is when you go into detail about your achievements and responsibilities.

Your current/most recent employment should be listed first i.e. in reverse chronological order. State the dates of the employment i.e. "March 2000 - to date", current title and employer's name. We suggest you give a brief introduction to the company and identify which division you worked within. If you have held more than one role within the same company ensure that dates are easy to identify.

Academic qualifications. Put your higher level qualifications first, such as a Masters or Bachelors degree. In you do not specify the classification (or GPA) of your degree on the CV, the reader will usually assume that it is a lower grade.

Training. Training courses are not regarded in the same way as academic qualifications so there is no need to list every single course you have attended.

IT Skills. For roles that require advanced technical abilities, such as statistical modelling, it is essential that you include relevant data. For example, if you have advanced SAS or SPSS skills ensure this is clearly identified. It is often useful to list some of the techniques you have used such as cluster analysis, conjoint analysis, multivariate regression, use of neural networks etc.

Interests. Give a flavour of your interests rather than an exhaustive list of all your past hobbies. Do not list activities in which you have not participated for several years. Avoid listing subjects that may raise controversy such a membership of a political party.

Once you've written your CV and checked it, run a spell check and then check it again. Mistakes on a CV will immediately put off the reader. Ask someone to read it for you and to tell you what they think.

    Sample format for Pharmacovigilance Job Application 

 Email  : 
 Mobile  : 

To,
 The HR Manager

Subject  : Application for the post of Patent Associate in your esteemed organization.

Sir/Mam,
With respect to the above-mentioned subject, I offer myself as a M.Pharm with having Three years experience in pharma sales and three month experience in IPR at Venus Remedies Baddi with dedication and commitment towards the responsibilities bestowed on me. I have the ability to come out with desired results.

I am herewith enclosing my detailed biographical particulars for your kind consideration and perusal.

Hope you would consider my candidature and provide me an opportunity to serve your reputed concern, for which I assure you the best of my service.

Thanking you
Yours sincerely,
ABC

CURRICULUM VITAE  :
Name

City

E.Mail-
 
OBJECTIVE  :

Seeking the position of a drug safety associate with a view to utilize my interest, credentials and work experience in the field of medical towards professional growth and development

Core Competencies:

• Comprehensive knowledge of international drug safety and pharmacovigilance principles and regulations
• Extensive knowledge of drug safety and drug development process and procedures
• In-depth knowledge of coding principles, submission criteria, regulatory timeline requirements, technical requirements and guidelines
• Possess sound communication skills, both in verbal and written
• Familiar with basic computer and database applications
• Good leadership, analytical, problem solving and time management skills

EDUCATIONAL QUALIFICATION  :
 M.Pharm in Pharmaceutical chemistry, SJCPS, Naharkanta, BBSR, under Biju Patnaik University of Technology, Orissa. Secured CGPA 8.2 on a scale of 10.
 B. Pharm fromIPT, Salipur, under Biju Patnaik University of Technology Secured CGPA 7.64 on a scale of 10.00.

Professional Experience:

Organization:
Duration:
Designation: Drug Safety Associate

• Handle responsibilities of reviewing and processing adverse events reported by investigators
• Perform the tasks of conducting research and analyzing medical and scientific literature
• Responsible for providing medical and scientific information to health care professionals
• Perform the tasks of reviewing bioequivalence study protocols, clinical trial protocols, and provide support the clinical trial team
• Handle responsibilities of developing concise, accurate and well-written case narratives
• Perform the tasks of maintaining the safety database and perform coding of diseases as well as adverse events according to the project-specific coding conventions
• Responsible for making presentation of safety process at clients and investigator meetings

Organization: Medico Clinic, California
Duration: April 2008 to December 2009
Designation: Junior Drug safety Associate

• Handle the tasks of assisting drug safety associate in checking the accuracy and cohesiveness of adverse event and serious adverse event
• Responsible for assisting drug safety associate in preparing and reviewing safety reports
• Perform the tasks of checking patient eligibility for clinical trials
• Handle responsibilities of entering data into the database and reporting systems
• Perform the tasks of assisting comprehensive reviews of serious-adverse events
• Responsible for drafting case narratives and processing case-related information

COMPUTER PROFICENCY  :
 OperatingSystem  : DOS, Windows- XP
 Office Packages  : MS.Office-2000/2007

PROJECT EXPERIENCE  :
M.Pharm
 HPLC method development and validation for VENLAFAXINE HYDROCHLORIDE formulation and its stability studies.

B.Pharm  :
 Pharmacological Screening and evaluation of ALOE VERA

SEMINAR  :
 M.Pharm  : HPTLC AND PROTONPUMP INHIBITORS
 B.Pharm  : PHARMACOLOGICAL SCREENING AND EVALUTION OF ALOEVERA
 
WORK EXPERIENCE  :
**

KEY RESPONSIBILITIES  :

 
PERSONAL INFORMATION  :
Date of Birth  :
Marital Status  :
Religion  : Hindu
Nationality  : Indian
Languages Known  : 
Strengths  : Communication skills, Punctuality, Self Confidence Willingness to learn, High degree of self motivation, Leadership Quality, hard working.

Reference:

Will be pleased to provide upon request 

DECLARATION  :
I hereby declare that the above information provided is true to the best of my knowledge and belief.
 
Date  :
Place :

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