Headquartered in Maryland,Bridge Laboratories is a company focused on high-quality and cost-effective preclinical drug development services in the US and China for the pharmaceutical and biotechnology industries. Bridge recently acquired Gene Logic Laboratories. The combined company has more than 300 employees, and the capabilities now include nearly all aspects of US/EU/JP regulatory compliant preclinical drug discovery and development services.
Bridge recently opened a state-of-the-art animal vivarium in China in the prestigious Zhongguancun Life Sciences Park in Beijing. This facility was designed from the ground up to US accreditation standards, and operates under US-level GLP standards.
Bridge is a globally integrated (China- and US-focused) preclinical CRO with US level state-of-the-art facilities; AAALAC and US-level animal welfare protection; validated software and data acquisition; strict data security and encryption; global customs and shipping logistics; quality animal supply; US-level quality assurance training and compliance; project management, US board certified pathology services, English-only SOPs together with a motivated; client-centric, and highly trained and experienced staff.
Please visit www.bridgelaboratories.com for further information. If the national firewall blocks the US site, Please try http://www.freeproxyserver.ca/index.php?btxmnercdeqt=aHR0cDovL3d3dy5icmlkZ2VsYWJvcmF0b3JpZXMuY29t&hl=3ed
Welcome the most energetic, excellent ones to join us for drug development in China.
公司地址：昌平區(qū)科學(xué)園路32號(hào)，中關(guān)村生命科學(xué)園區(qū)內(nèi)
郵政編碼：102206
電子郵箱：hr@bridgelaboratories.com or hr@vitalbridge.com.cn
招聘職位信息：
1. Toxicologist - Beijing, PRC
The Toxicologist II will collect, document, and manage pertinent data including animal observations, test material administration, and clinical sample collection in compliance with appropriate SOPs, GLPs. He or she may serve as study director in the conduct of toxicology studies.
Responsibilities:
· Follow study protocols and SOPs
· Report to Study Directors in a timely manner regarding any deviations from protocols or unexpected results
· Contribute to protocol drafting, study preparation, quality control study data and final report drafting.
· May contribute to SOP drafting and revising.
· Provantis training, problem solving for end users, system libraries maintenance.
· Recognize deviations, determine course of action, including notifying supervisor and document appropriately.
· Review data and identify potential problems
· Train and instruct less experienced staff
· May serve as Study Director in the conduct of toxicology studies.
Requirements:
· Master’s or PhD degree (PhD preferred) in medicine, biology or veterinary medicine
· Work experience in related fields preferred
Bridge recently opened a state-of-the-art animal vivarium in China in the prestigious Zhongguancun Life Sciences Park in Beijing. This facility was designed from the ground up to US accreditation standards, and operates under US-level GLP standards.
Bridge is a globally integrated (China- and US-focused) preclinical CRO with US level state-of-the-art facilities; AAALAC and US-level animal welfare protection; validated software and data acquisition; strict data security and encryption; global customs and shipping logistics; quality animal supply; US-level quality assurance training and compliance; project management, US board certified pathology services, English-only SOPs together with a motivated; client-centric, and highly trained and experienced staff.
Please visit www.bridgelaboratories.com for further information. If the national firewall blocks the US site, Please try http://www.freeproxyserver.ca/index.php?btxmnercdeqt=aHR0cDovL3d3dy5icmlkZ2VsYWJvcmF0b3JpZXMuY29t&hl=3ed
Welcome the most energetic, excellent ones to join us for drug development in China.
公司地址：昌平區(qū)科學(xué)園路32號(hào)，中關(guān)村生命科學(xué)園區(qū)內(nèi)
郵政編碼：102206
電子郵箱：hr@bridgelaboratories.com or hr@vitalbridge.com.cn
招聘職位信息：
1. Toxicologist - Beijing, PRC
The Toxicologist II will collect, document, and manage pertinent data including animal observations, test material administration, and clinical sample collection in compliance with appropriate SOPs, GLPs. He or she may serve as study director in the conduct of toxicology studies.
Responsibilities:
· Follow study protocols and SOPs
· Report to Study Directors in a timely manner regarding any deviations from protocols or unexpected results
· Contribute to protocol drafting, study preparation, quality control study data and final report drafting.
· May contribute to SOP drafting and revising.
· Provantis training, problem solving for end users, system libraries maintenance.
· Recognize deviations, determine course of action, including notifying supervisor and document appropriately.
· Review data and identify potential problems
· Train and instruct less experienced staff
· May serve as Study Director in the conduct of toxicology studies.
Requirements:
· Master’s or PhD degree (PhD preferred) in medicine, biology or veterinary medicine
· Work experience in related fields preferred