Franchisee Offerings Announced by Helix Research Center Ltd,for Clinical Research Training Worldwide

July 16, 2010 - PRLog -- The Founder of Helix Research Center Ltd;Dr Venkateswar Rao G,has passion for Education,especially Continuing Education Programs.He has been nurturing the talent of aspiring Life Science background candidates from across the Globe since a Decade.
Since,there are millions of  highly talented youngsters across the Globe,who wish to become Clinical Research Professionals,Helix Research Center Ltd has taken the iniaitive to make 'Clinical Research Training Programs ' avaiable in Each and Every Country of the World for a nominal fee.The best possible Solution to offer the Training Programs nat a lower cost is by offering Franchisees to Local companies/Individuals who wish to promote  Clinical Research Programs,apart from their day today activities.This would reduce Infrastructure cost, Training and administrative expenditure.
Helix Research Center Ltd invites applications from prospective Franchise owners to explore the possibility of working together.
Helix Research Center Ltd would use avaialbe  modern technology to impart Quality Training to aspiring freshers with Life Science background.Helix Research Center is also exploring working relation with various Hospitals from across the Globe to place Clinical Trials and or make the Hospitals ready to expedite Clinical Trials as per ICH GCP Guidelines.Hence,the employment opportunities for Trainees,post Training would significantly increase.
Candidates with Life Sceince background,who possess excellent Communication skills invariably do well as Clinical Research Professionals.
Following is the list of Training Programs ,being offered by Helix Research Center Ltd Worldwide.
1.Clinical Research Associate
2.Clinical Research Coordinator
3.Clinical Research Investigator
4.Clinical Data Management
5.Quality Assurance
6.Regulatory Affairs
7.Research Nurse
8.Biostatistics
9.Pharmacovigilance
10.SAS  and Oracle Clinical
Mode of Delivery:
Online
Inclass
Online + Inclass

Upon completion of Training,all the Trainees would get 'Certificate of  Completion' of the particular Course.
Since Human Subjects are involved in Clinical Trials,Helix Training Programs would provide necessary skills and knowledge required to ensure Safety and well being of the Human subjects taking part in Clinical Trials.Helix Programs would also provide necessary skills  for the Trainess to perform their duties as Clinical Research Associates,Clinical Research Co-ordinators or Study Co-ordinators,Quality Assurance/Regulatory Affairs/Clinical Data Management Professionals ,Research Nurses etc.
The the Best and Only way to become a Clinical Research Professional is to start working on real projects and hence we advise all the aspiring candidates ,not waste their precious time reading only  theory.The moment a candidates thinks of becoming a Clinical Research Professional,He/She should start applying for  jobs  Pharma,Biotech,Medical Device and Cosmetic companies,Contract Research Organisations(CROs),Site Management Organisations(SMOs),Investigative Sites,Alliance of  Hospitals;Non SMO,Global boides like World Health Organisation,National Institiute of Health(NIH), etc.
Helix Research Center Ltd provides Free Career Guidance any aspiring Candidate from any Country.Candidates are welcome to directly contact ,Dr Venkateswar Rao G,Chairman of Helix Research  Center Ltd .He could also be contacted on Twitter;http://twitter.com/chairmanhelix and on Facebook:http://facebook.com/HelixWorld.
Helix Research Center is also open to working with any Non Profit ,Voluntary Organisations,Professional Associations,Universities,Academic bodies inorder to impart Quality Training to all the aspiring Life Science Gradautes,Post Graduates and P.hDs from across the Globe.
Clinical Research has been a Multibillion Dollar Stable Industry for over 100 years and it is fast emerging as 'Most Lucrative'Profession Globally.The reason is ,most of the Global companies such as Accenture,Infosys,TCS,Wipro,LG,Philips,Cognizant ,etc have established Consulting divsions for Pharamaceutiical,,Biotech.Medical Device and Cosmetic companies.Pharmacovigilance  Services are being offered by almost all the Global BPOs and hence candidates who have basic knowledge of ICH GCP-International Conference on Harmonisation,Good Clinical Practices are being rapdily absorbed into these companies.The starting salaries for Clinical Research Professionals is at par with IT Professionals and Clinical Research Professionals are invariably paid more than IT Professionals if they prove to be 'Assets 'for the Organisation they work for.
Even though ,any Life Science candidates is eligible to work as a Clinical Research Professional,the Actual Life science division varies from country to country.For example,in the United Sates of America,candidates with Nursing background  prefer to become Clinical Research Professionals,whereas in some other countries,Pharmacy,Microbiology,Biotechnology,Biochemistry  candiidates opt for Clinical Research as  career.
Research and Development (R&D) divsions Sponsor companies;Pharmaceutical,Biotechnology,Medical Device,Cosmetic companies etc are engaged in the persuit to discover new Drugs.According to avaialbe statistics,if 5000 compunds with medicinal property are tested,only 1  compund is approved as a New Drug to be manufactured and marketed.The average expenditure incurred by Sponsor to bring a new molecule to the market is around USD 600 to 900 Million!.
The Experimentation done on animals is called as 'Pre-Clinical Research' and that carried out on  Human beings is a Clinical Trial;Phase I through IV.In view of huge expenditure involved in R&D activities and Strict Timelines set by the Sponsor to successfully complete a Clinical Trial,all the Personnel working in Clinical Research Arena should possess thorough knowledge of Guidelines and Regulations pertaining to Clinical Research/Clinical Trials.
The Sponsor company;Pharmaceutical,Biotechnolgy,Medical Device and Cosmetic company or any other Organisation hires the services from CROs-Contract Research Organisations to expedite one or more Clinical Trials related tasks.CROs play a  Crucial Role in Conducting and completing a Clinical Trials and CROs adhere to utmost Ethics and Punctuality to carry out Clinical Research activities.Clinical Trials;Phase I through IV are conducted at Hospitals,though  some times Phase I studies are conducted at Bio Equivalence(BE) facilities.Hospitals where the Clinical Trials are conducted are known as Investigative Sites.When a group of Hospitals are brought under same banner with same SOPs-Standard Operating Porcedures,they are known as SMOs-Site Management Orgnisations.Some Hospitals form an Allaince to conduct Clinical Trials ,in Non SMO model.
Hence the aspiring candidates can apply for jobs with the Sponsor,Contract Research Organisations,Site Management Organisations,or at Investigative Sites,.
The typical designations used for Clinical Research Professionals are ;CRA-Clinical Research Associate,CRC-Clinical Research Co-ordinator,RA-Regulatory Affairs,QA-Quality Assurance ,CDM-Clinical Data Management professionals.
The employment opportunities with Pre-Clinical CROs,BA/BE CROs-Bio-Availability and Bio-Equivalence are also very promising.
Clinical Research Professionals should always give importance for Continuing Education and also enroll for the Memberships of Global bodies of Clinical Research Professionals such as Association of Clinical Research Professionals(ACRP),Regulatory Affairs Professional Society(RAPS),Drug Information Association (DIA),Society for Clinical Data Management (SCDM) ,Society for Clinical Research Associates (SoCRA ) etc.
These Professional bodies conduct 'Certification' Exams for experienced Clinical Research Professionals from all over the World.
Certificate Issued by these bodies is well respected by the Clinical Research Industry Worldwide.
Join the Initiative taken by Helix Research Center Ltd to nurture Talent!

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Helix Research Center Ltd is a London(UK) based global company offering Contract Research,Training,Auditing,Consulting,Medical Writing,Pharmacovigilance,Biostatistics,SMO,Regulatory Affairs,Quality Assurance,Publications,Translation ,CDM services globally