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research Scientist II, Biomarkers You are ... Biomarkers You are here: Home research Scientist II, Biomarkers research Scientist II, Biomarkers Req ID: ... Req ID: 15257 Job Category: research Location:..
... growth and actively recruiting Clinical Research Coordinators. The Clinical Research Coordinator (CRC) will be responsible ... of 3 years of related research support experience; or the equivalent ... ability..
... process. Lead the development of research plans, protocols and budgets, conducts ... perform health economic and outcome research projects/studies focusing on value, positioning, ... project management, including selection of..
How to Apply:
Job #: 19205
Clinical Trial Project / Study Manager
Job Location: Norwalk, Connecticut - United States
Salary: $130,000.00 - ..
Summary The EHS Coordinator will be responsible for partnering with Client site personnel from various departments to carry out day-to-day EHS tasks, develop site SOPs, track and manage EHS site metrics, ..
Stryker is one of the world’s leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care. The Company offers a diverse ..
Overview Do you have a noticeable passion for results? Youu2019re bold, empathetic, and very resourceful, especially when results are at stake. You have what it takes: a competitive drive coupled with ..
u003Cpu003Eu003Cfont size=4\u003Eu003Cbu003Eu003Cuu003EClinical Trial Manageru003C/uu003Eu003C/bu003Eu003C/fontu003Eu003C/pu003Eu003Cpu003Eu003Cbu003EPosition Overviewu003C/bu003E: The Clinical Trial Manager will be responsible for all aspects of study conduct and CRO oversight and the primary point of contact for clinical study project ..
The Toxicology Technician is responsible for performing accurate, high quality in-life study work for rodent and non-rodent safety studies in compliance with the study protocol, Standard Operating Procedures (SOPs), ..
Description: The Director, Payor Access Marketing is responsible for managing a team to deliver a positive experience with payor customers which leads to optimal brand access. Director of Payor Access Marketing ..
ROLE SUMMARY We are seeking an experienced Molecular and Cellular Biologist with experience in transcriptomics (DNA/RNA/single cell sequencing in frozen and fixed tissues) to join our nonclinical Investigative Toxicology team in ..
... and maintains a variety of research protocols with hospital, sponsor, and ... diagnostic techniques, and enhancing the research group's ability to acquire research funds. Qualifications Bachelor's Degree, Master's .....
... for the development of clinical research protocols, clinical study reports, and ... and emerging data of ongoing research projects within and outside the ... study managers and directors, clinical..
... and maintains a variety of research protocols with hospital, sponsor, and ... diagnostic techniques, and enhancing the research group's ability to acquire research funds. Qualifications u2022Bachelor's Degree, Master's .....
Clinical Research Assistant 2 in New Haven ... Yale-New Haven to advance cancer research, prevention, and patient care, as ... outreach and education. The Clinical Research Assistant (CRA) will provide..
... expertise when working with site Research and Development teams, facilities team, ... investigations and EHS audits of Research and Development labs and facilities ... systems supporting office, manufacturing, and..
... Collaborate with members of Clinical Research and Marketing, Trial Clinical Monitor ... be sent to the contract research organization (CRO). From a statistical ... with other functions including Clinical..
ROLE SUMMARY This is a scientific and business leadership position in the Global Investigative Toxicology line (~35 colleagues) in Global Drug Safety Research and Development (DSRD; ~450 colleagues). The remit of ..
ROLE SUMMARY The DSRD Regulatory Operations Lead is located in the Regulatory Strategy and Compliance (RSC) of Drug Safety Research and Development (DSRD and is responsible for supporting the submission of ..
As part of the Data Monitoring and Management (DMM) group, an integral delivery unit within the Global Biometrics and Data Management (GBDM) organization, the Clinical Data Standards Lead is ..
Develop policies, initiatives, procedures and training to ensure compliance with ever evolving Federal, State and Local EHS related regulations.
Assist with managing third party vendor relationships including hazardous waste haulers, consultants ..
... Degree Skills Project Management Clinical Research Strategic Planning Benefits Health Insurance ... Project Director. SUPERVISION EXERCISED: Supervises research assistants/associates/technicians, clerical or other staff ... safety of subjects in clinical..