www.artemishospital.in Artemis Health Institute Gurgaon : Technologist Radiation Oncology

[muthukalee]

Designation : Technologist Radiation Oncology

Job Description : To ensure error free tests in the Deptt. To participate in the on going education for all staff in the Deptt. To maintain highest standards of patient care. To support the implementation of service excellence programme. Handling of grievances of patients & the internal staff.

Skill Set : Strong critical thinking, problem solving and attentiveness to detail required. Excellent oral and written communication skills are essential. Demonstrates accuracy and an attention to detail.

Qualifications : Recognized Degree / Diploma in Radiation Therapy Technology from an institution approved by concerned Statutory bodies of Govt. of India.

Experience : 0-3 years of Experience

Apply : http://www.artemishospital.in/applyonline.php

About us :
Artemis Health Institute (AHI), at Gurgaon is a NABH Accredited, 260-bed tertiary care super-specialty flagship hospital established by Artemis Health Sciences (AHS) - a healthcare venture launched by the promoters of the Apollo Tyres Group. Artemis aims at creating an integrated world-class healthcare system by leveraging the best medical practices backed by cutting-edge technology. The super-specialties chosen by Artemis as its area of focus include Cardiovascular (Heart), Oncology (Cancer), Orthopedics & Joint Replacements, Neurosciences and Bariatric & Minimally Invasive Surgery in addition to host of other specialties.

Contact us :
Artemis Health Institute
Sector -51,
Gurgaon - 122001
Haryana, INDIA.

http://www.artemishospital.in

[Guest-IJT]

Name : Rahul Roy
Email : mail2rahulroy AT yahoo.com
Designation / Skillset : Team Leader

Subject : Application For the suitable post in pharmacovigilance.
Respected Sir/Madam,
I am Rahul Roy, a B-Pharma graduate having more than 2 years of experience in Pharmacovigilance in USA and EU Processes, presently working as a Team Leader, with great interest and enthusiasm in the field of pharmacovigilance would like to offer my candidature for your kind perusal and consideration.
Though my resume summarizes my professional and academic history, there is much more to relate. I would appreciate an interview with you to further discuss my qualifications as well as learning about your requirements and organizational objectives. I am confident that with my motivation and sense of responsibility, I can quickly become a productive member of your staff. If I will be given an opportunity to serve your esteemed organization, than I shall prove myself to the best of my knowledge and capabilities. I look forward to hearing from you soon, and appreciate your time and consideration of my candidacy.
Thanking you for your kind cooperation and consideration.
Yours truly.
Rahul Roy
Date :
Place- New Delhi.

Resume :

SYNOPSIS
- A result oriented professional with more than 2 years of experience in Pharmacovigilance.
- Well versed with both USA and EU Pharmacovigilance Processes.
- Presently working with APCER Pharma Solutions Inc as Team Leader USA Process.
- Complete Team Management and Leadership skills.
- Well versed with VOL 9A - Volume 9A of the “Rules Governing Medicinal Products in the European Union : Pharmacovigilance for medicinal products for human use”.
- MedDRA coding proficiency.
- ARISg (Adverse Reaction Information System Global)Expertise.
- Complete knowledge of Overall Pharmacovigilance Practices for both USA and EU Processes including Case Processing, Quality Check, PSUR compilation, PADER compilation, Generation of Line-listings, Literature search among other Pharmacovigilance related work.
- Medical Writing : Drafting and review narratives for the innovator clinical trial data and creating high standard scientific documents especially for oncology products. Basic training by BAYER on medical writing and narrative creation.
AREAS OF EXPERTISE
Current Job profile
The scope and scale of activities with which this job is concerned and is involved as TEAM LEAD
- Managing a team of 10-12 people.
- Manage daily workload in conjunction with Pharmacovigilance Manager for individual case processing, literature searches, PSUR generation and any other tasks relevant to the Pharmacovigilance Department.
- Data Entry and Quality Check of ICSRs in APCER's pharmacovigilance database (ARISg) and other case management activities
- Signal Detection of the ADRs with cases received for client's products
- Generation and review of SOPs and WPDs
- Execution of Company Standard Operating Procedures
- Management of Compliance with the Company Standard Operating Procedures and regulatory requirements
- Liaise effectively and maintain excellent relationship with the clients and internal/external contacts
- Maintain awareness of changes to/new regulations affecting Pharmacovigilance activities. Communicate new or changed regulations to management and to relevant members of the department in order to initiate any change in processes
- Builds and maintains good relationships across functional units and company affiliates
- Trains and mentors new employees in pharmacovigilance
- To carry out necessary administrative duties required for the job
- To contact, as required, UK / US office(s) and customers/clients in order to achieve required outcomes and meet timelines
- Other duties as assigned by management
- To monitor and disseminate information on changes in the regulatory requirements (USA and Europe) by checking relevant websites and journals
- Manage daily workload in conjunction with Medical Affairs and Pharmacovigilance Manager for individual case processing, literature searches, PSUR generation and any other tasks relevant to the Pharmacovigilance Department
- Liaise with other Pharmacovigilance executives and Pharmacovigilance Officer to manage individual case processing timelines and quality check as necessary
- Follow-up of serious and non-serious cases
- Medical Writing : Drafting and review narratives for the innovator clinical trial data and creating high standard scientific documents especially for oncology products.
The scope and scale of activities with which this job is concerned and involved as Pharmacovigilance Associate :
- Preparation and review of Periodic Safety Update Reports (PSURs). It also requires managing the PSUR process involving intradepartmental and interdepartmental coordination. In a span of two years, have prepared more than 90 PSURs and have reviewed 20 PSUR’s.
- Review and preparation of Periodic Adverse Drug Experience Reports (PADER) for submission to USFDA.
- Managing case processing by case triaging and assigning Data entry, Quality check (QC) of cases for submission to Regulatory Authorities in EEA and FDA in ARISg Database.
- Processing of ADR cases in ARISg database.
- Data Entry of cases done – (˜700)
- Quality Control Review of cases done – (˜900)
- Actively participated in audit of Pharmacovigilance system in Dec 2009 and May 2010 and was able to complete without any critical findings.
- Review and verify appropriate selection of adverse events from source documents, appropriate MedDRA (Medical Dictionary for Regulatory Activities) code for each adverse event and accuracy of product label assessments for each adverse event.
- Interact with client to resolve queries related to the processing of safety data.
- Review the source document to assure relevant information pertaining to the case is appropriately entered into the database fields.
- Handled Spontaneous cases, Prepared ADRs forms, telephonic contact record and closed the case satisfactorily.
- Support to team at US office for management of adverse reaction processing process and product quality complaint handling process.
- Management of the Adverse Drug Reaction processing by the team to ensure compliance to the regulatory obligations and effective case processing.
- Co-ordinated in development of SOPs and working guidelines for maintaining quality standards in the work and to comply with regulations.
- Query Handling. Follow-ups/Administrator work on ARISg/CPD updation /Literature articles to review/Data Entry-Quality Review/Report Scheduling of the literature articles.
- Co-ordinated in preparation and review of Safety Data Exchange Agreements (SDEAs).
Trainings Attended :
- Training on PSUR generation
- Training on MedDRA
- Training on Leadership skills and effective communication
- Training on “Managing Self and Others”
- FDA guidance on adverse reactions and CFR regulations
- Training on applicable parts of VOL 9A - Volume 9A of the “Rules Governing Medicinal Products in the European Union : Pharmacovigilance for medicinal products for human use”.
- Training on ARISg (Adverse Reaction Information System Global).
- Training on SOPs and Guidelines.
- Medical Writing : Basic training by BAYER on medical writing and narrative creation for the clinical trial data especially for oncology products.
PROFESSIONAL DETAILS
Since Jan’09 at APCER Pharma Solutions as a Team Leader based in Delhi.
March 2005 - Oct 2008 : Ronson Pharmaceutical Ltd.
As Customer relation manager (CRM).
Apr 2001-Jan 2005 : Raptakos, Brett& Co. Ltd
As Business Executive.
ACADEMIA
- B.Pharma (Hons.) (Pharmacy) from Sambalpur University in 2001.
- Certificate in Pharmacovigilance & Pharmacoepidemiology from Symogen, India.
- MBA (Marketing) from Symbiosis, Pune (continuing through distant learning).
- Computer Skills :
Operating system : Windows Vista, XP
MS word, MS excel, MS power point, proficient in internet research.
PERSONAL DETAILS
Date of Birth : 13 June 1976
Address : 12/25, IIIrd Floor, Subash Nagar, New Delhi-110027.
PERSONAL Attributes :
A highly motivated, hardworking and dependable person. Punctual, reliable and willing to learn.
Able to work both independently and in a team with a good eye for detail. Able to organize and
integrate individual efforts into a team. A team player with a flair for motivating collogues. Work to ensure that internal and external timelines are met.
Decalaration :
I hereby declare that all the information given above is true to my knowledge. All the documents in original/attested copies will be produced whenever required.

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More Information about this submission and submitter:-
___________________________________________________
Submission ID : 4145101
Date & Time : 18th May 2011 5:45 AM (UTC)
IP Address : 122.162.138.34
Browser Info : Mozilla/5.0 (Windows; U; Windows NT 5.1; en-US; rv:1.9.1.19) Gecko/20110420 Firefox/3.5.19 ( .NET CLR 3.5.30729)
Predicted Country : India

[Guest]

CURRICULUM VITAE
RICHA SHARMA
Email : richa.icri AT yahoo.com
Career Objective :
To be a part of a dynamic organization, assist my colleagues and seniors in fulfilling organizational goals and to achieve a successful and respectable position through my knowledge and hard work.
Professional Qualification :
Course Institute Year
Bachelor of Dental Surgery(B.D.S.) M.N.D.A.V. Dental College & Hospital, Solan, H.P. affiliated to Himachal Pradesh University, Shimla.H.P. 2003-2007
1 year Rotatory Internship Training M.N.D.A.V.Dental College &Hospital. 2007-2008
MSc. Clinical Research
(Pursuing) Institute of Clinical Research India,ICRI,Delhi affiliated to Cranfield University,U.K. 2010-2011
Educational Summary :
Class Board Institute Year of Passing
Xth C.B.S.E. D.A.V.Public School Palampur 2000
XIIth C.B.S.E. D.A.V.Public School Palampur 2002
Projects :
Submitted various projects and gave presentations on various
topics during Post graduation &Graduation for e.g.
- TGN1412 Humanized Agonistic Anti-CD28 Monoclonal Antibody.
- Viscosupplementation
- Epilepsy
Achievements :
- Qualified IELTS Examination in 2010 with 7 bands.
- Scored first position in the state in a talent search examination and received prize and certificate from Director of Education, Himachal Pradesh in 2000.
Area of interest :
Medical Writing, Clinical Research Coordinator, Medical Coding &Pharmacovigilence
Strengths :
- I am a sincere person and totally dedicated towards the task I undertake.
- I am a team player
- Well accustomed with Microsoft word,Microsoft power point(2007) in the field of computer
- Good communication skills

[Guest]

CURRICULUM-VITAE

Narendra singh
Email ID : narendrasingh9627 AT gmail.com
CAREER OBJECTIVE :
· To serve an organization with work environment conducive to exposure and use my abilities to
Achieve organization goals.

ACADEMIC QUALIFICATIONS :
· B.Sc. from Jaipur University in 2011.
· Intermediate from Rajasthan Board Ajmer in 2000.
· High School from Rajasthan Board, Ajmer in 1998.

PROFESSIONAL QUALIFICATIONS :
Diploma in Medical Radiotherapy&Radiography in 2001-03 .
WORKING EXPERIENCE :
I have seven years experience in the department of radiation oncology as a radiation technologist on different types of machine like that Cobalt 60, Theratron 780, Electra linear accelerator, Seamen’s simulator, Seamen’s Primus linear accelerator and others.

TECHNICAL SKILLS :
Basic knowledge of computer & internet.
I handle special procedure like that blood irradiation, whole body irradiation.
I attend AROI conference at Ludhiyana.

STRENGTHS :
· Positive Attitude, punctuality, teamwork, leadership qualities and hardwork.

HOBBIES/INTERESTS :
Listening to Music
Making friends, interacting with new people.