CRAs - Join Covance and receive a $5000 Sign On Bonus!
Experienced Clinical Research Associates (CRAs)/Monitors: We are hiring Phase I-IV CRA positions.
Positions are home-based and needed throughout the United States.
All therapeutic areas needed. Please let us know your therapeutic experiences on your resume.
Focusing on balance and quality by only working on 1 to 2 studies!
Our Clinical Research Associates /CRAs / Monitors manage all aspects of site monitoring responsibilities for ...
Radiant Research (radiantresearch.com) is comprised of 20 wholly-owned premier clinical research centers nationwide. Our clinical research centers provides a critical service to biopharmaceutical companies by recruiting study participants into clinical research, conducting the clinical research protocol and collecting the data necessary to support the safety and efficacy of the drug company's product to the FDA. Our client list includes every major pharmaceutical company and contract research ...
CONTRACT / ALMOST 3 YEARS
MUST HAVE..GCP, ICH,SIP AND KNOWLEDGE OF FDA REGULATIONS
SPANISH A BIG PLUS !!!!!!
Coordinate delivery, collection, and review of trial documents to and from investigator sites, and the GCSM organization.
Ensure clinical site documentation is done in accordance with the client’s Standard Operating Procedures (SOPs), Good Clinical Practice (ICH-GCP), Good Business Practices, and applicable regulatory requirements.
Coordinate delivery and collection of trial documents to ...
We are currently seeking office-based Project Directors and Clinical Trial Managers to join a global Clinical Operations team in their new Dallas-based office. This is a chance to work with a mid sized company that is growing. We are looking for candidates that want the chance to grow professionally with the company.
Operational execution of global multiservice clinical trials, including coordination of project start-up, maintenance throughout the study stages, and coordination of ...
The responsibility of the CTMS Administrator is the oversight and coordination of all activities that involve the Clinical Trial Management System and Alcon Technology Platform for Clinical Development used in the planning, execution and reporting of Alcon’s Clinical trials. The incumbent must collaborate effectively with Clinical Trial Management (CTM), Global Clinical Site Management (GCSM) and Clinical Data Management (CDM) and R&D Finance to produce an efficient solution for managing ...
1. The incumbent will serve as the single point of clinical pathology services in support of in vivo exploratory and GLP-regulated preclinical safety studies utilized in government submissions and product development activities.
2. The incumbent will have accountability for management of a preclinical laboratory responsible for the conduct of hematology, clinical chemistry, coagulation, and urine analysis of biological samples collected from a variety of preclinical test systems. The incumbent will ...
We are looking for a Regional CRA Based out of the MW to work for a mid-size CRO. This will be an exciting opportunity to work for a company that is growing. The company is looking for people that are interested in growing with the company. They do this by promoting from within!
DESCRIPTION OF JOB DUTIES
Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to Comany/Sponsor SOPs and GCP;
Maintain ongoing site correspondence and site files;
Precept Life Sciences is seeking experienced Regional CRAs across the country for permanent positions with several leading CROs.
On average, CRAs are assigned to an average of 12 sites across 1-3 protocols. Study and site assignment will vary depending on monitoring duration/frequency, location of sites and complexity of trial.
CRAs are expected to be 80% billable, with approx. 60% travel.
We are looking for CRAs that are not just field monitors, but those that manage all aspects of the site ...
*RELOCATION to San Francisco Bay Area/Silicon Valley Required (relocation assistance provided)*
This role will immediately assume study lead data management responsibilities for 3-5 concurrent clinical trials within Oncology, Respiratory or Liver Disease, utilizing primarily the Medidata RAVE electronic data capture and management system. The selected candidate will manage trials in various stages, from planning, to set-up, conduct, closeout, and archiving, in high volume, while maintaining a high ...
Lead technical activities to demonstrate preclinical efficacy of implantable ocular devices through in vivo, ex vivo and in vitro studies to support various projects within Alcon’s Cataract Surgery business.
1). Conduct preclinical efficacy studies (design-of-experiments, execute experiments, collect and analyze data with robust application of biostatistical methods) to support R&D projects in Alcon’s Cataract Surgery (Intra-ocular lenses) business.
2). Accountable for preparing and presenting ...
Oct 17 -
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