Clinical Research Staffing Firm ASG Acquires CR ckham …
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- Clinical Research Staffing Firm ASG Acquires CR ckham …
- » Clinical Research Associate
- New Clinical Trial Customers Punctuate Success of Phase Forward …
- EyeGate Pharma Completes Phase II Clinical Trial of EGP-437 for …
- Local clinical trials offer help to patients with the disease
Clinical Research Staffing Firm ASG Acquires CR ckham …
PR Newswire (press release)
- a high-quality functional outsourcing and specialty staffing services group based in Cary North Carolina – has acquired neighboring ckham Development Group Inc. a full-service contract research organization. The acquisition – completed in early February for an undisclosed amount of stock – enables ASG to expand the breadth and value of services it provides clients needing to outsource clinical research trials; it also equips its clients in the pharmaceutical industry with a robust package of functional outsourcing and staffing services as well as a new opportunity to outsource an entire clinical trial. “The addition of the ckham team and its services helps accelerate our goal of becoming the company of choice for those wishing to outsource or augment staffing of a clinical trial” said ASG President and CE James Baker. “We now have the breadth of services that allows clients to one-stop shop if they so desire. In completing the acquisition ASG is fulfilling a portion of its global growth strategy that will allow the firm to provide solutions that best meet the needs of existing and potential clients. At the same time the acquisition will make it possible for ckham – which will continue to be independently branded – to serve a wider and larger client base.
» Clinical Research Associate
Hays Pharma
00 per annumLocationRussia – Moscow03 Mar 2009The great opportunity has arrived to join leading Pharmaceutical Company for the position of Clinical Research Associate located in Moscow. Responsibilities: -Participate in site nomination process; perform evaluation of site capability and make recommendation for inclusion in clinical trial -Assume ambassadorial role to facilitate communication between sites and Key Novartis line functions to increase value proposition to investigators -Facilitate preparation and collection of site level documents -Execute site initiation and training activities -Perform monitoring visits according to monitoring plan -Manage site drug supply management -Resolve site level update of technical systems (Clin. Admin EDC) -Ensure site activities in line with milestones (i. start-up recruitment closeout etc.
New Clinical Trial Customers Punctuate Success of Phase Forward …
Business Wire (press release)
Across all of its solutions Phase Forward has over 90 CR customers as of the end of 2008. Medpace is a leading global full-service clinical research organization led by top therapeutic and regulatory experts who are driven to further the advancement of pharmaceutical agents for use in cardiology metabolism oncology and nephrology. Medpace has assembled the industry’s most experienced and therapeutically focused team to execute at every level of the company’s operations providing complete and seamless drug development services. Through specialized regulatory expertise and therapeutically focused clinical operations Medpace creates strategic partnerships with pharmaceutical and biotechnology companies to provide the most efficient and cost-effective path to drug development – from program planning and execution to product approval.
EyeGate Pharma Completes Phase II Clinical Trial of EGP-437 for …
MSNBC
The results of this study are expected inthe second quarter of 2009. For the dry eye clinical trial EyeGate worked with ra Inc. a leadingglobal clinical research and development organization located in AndoverMA. ver the past 30 years ra has played a central role in thedevelopment and FDA approval of more than 30 ophthalmic products. This Phase II single-center randomized double-masked placebo-controlledstudy of 89 patients evaluated the safety and efficacy of a corticosteroidsolution administered by the EyeGate® II Delivery System (at two doselevels) twice over a three-week period. ra’s proprietary ControlledAdverse Environment (CAE) clinical model was used for this study.
Local clinical trials offer help to patients with the disease
Bradenton Herald
comp –> Dix credits her success in part to her participation in a clinical research trial under the supervision of Dr. Louis Chaykin at Meridien Research 1105 53rd Ave. Suite 203 in Bradenton. “I’m so thankful for this program” Dix said.
Related from Managementmonster: MedAssurant Heart Failure and Diabetes Programs Receive Full NCQA …
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