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Sub Investigator for clinical trials - Bangalore
Sunday, 15 November, 2009
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Item details
City:
Bangalore, Karnataka
Salary:
Rs 40,000
Item description
We are a Site Management Organization with our headquarter in New York, USA and we have sites in various countries around the world.
Our Purpose
To support the innovation & development of new drugs & devices through clinical trials in partnership with pioneering pharmaceutical, biotechnology, and medical device industries.
Our Goal
To provide quality service, responsiveness, and results to our customers striving to be the finest resource & meeting their specific and unique needs.
We have pre-screened, highly experienced, suitably qualified, and enthusiastic Principal Investigators for clinical trials in virtually any specialty in various location worldwide ranging from an independent practitioner to a large network of physicians in hospitals & academic medical centers.All our Investigators meet the specific selection criteria outlined by the Sponsor or CRO.
We ensure timely and accurate regulatory board submission and data collection.
All sites have experienced, licensed, full time and dedicated clinical research professionals comprising of both clinical and non clinical team to ensure the prioritized and accurate submission of regulatory documents, appropriate site orientation /initiation, patient recruitment as well as the collection of clean and accurate data. Our sites are equipped with latest technology, in house lab facility to a central lab access for timely management of large number of patient lab. We have internal management and quality assurance system in place to ensure prompt and accurate completion of task and proactive handling of problems that may jeopardize the success of the trial.
We provide access to a large patient study population with an international approach.
We assess the sites for study patient population even before presenting an investigator thereby increasing the likelihood of enrollment goals. We make use of both carefully orchestrated advertising as well as site's own patient population or internal referral base to enroll patients.
Our Purpose
To support the innovation & development of new drugs & devices through clinical trials in partnership with pioneering pharmaceutical, biotechnology, and medical device industries.
Our Goal
To provide quality service, responsiveness, and results to our customers striving to be the finest resource & meeting their specific and unique needs.
We have pre-screened, highly experienced, suitably qualified, and enthusiastic Principal Investigators for clinical trials in virtually any specialty in various location worldwide ranging from an independent practitioner to a large network of physicians in hospitals & academic medical centers.All our Investigators meet the specific selection criteria outlined by the Sponsor or CRO.
We ensure timely and accurate regulatory board submission and data collection.
All sites have experienced, licensed, full time and dedicated clinical research professionals comprising of both clinical and non clinical team to ensure the prioritized and accurate submission of regulatory documents, appropriate site orientation /initiation, patient recruitment as well as the collection of clean and accurate data. Our sites are equipped with latest technology, in house lab facility to a central lab access for timely management of large number of patient lab. We have internal management and quality assurance system in place to ensure prompt and accurate completion of task and proactive handling of problems that may jeopardize the success of the trial.
We provide access to a large patient study population with an international approach.
We assess the sites for study patient population even before presenting an investigator thereby increasing the likelihood of enrollment goals. We make use of both carefully orchestrated advertising as well as site's own patient population or internal referral base to enroll patients.