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. Oncology experience URGENTLY needed.
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 Clinical trials, according to ...
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 ...
· Coordinates Post Market Reviews of Commercial Products including:
· Set up Power Point presentation based on established templates
· Coordinate timely execution of Post Market Review including set up and facilitation
· Follow-up to retrieve supporting data.
· High level review of data prior to post market review meeting
· Follow-up to gain approvals in a timely manner
· Archival of approved post market reviews
• Coordinates Post Market Reviews of Commercial Products including:
• Set up Power Point presentation based on established templates
• Coordinate timely execution of Post Market Review including set up and facilitation
• Follow-up to retrieve supporting data.
• High level review of data prior to post market review meeting
• Follow-up to gain approvals in a timely manner
• Archival of approved post market reviews
• Work with Risk Assessment Report Writer to ensure results of Post ...
Precept Life Sciences is currently seeking full-time Clinical Trial Managers to join a global Clinical Operations team with one CRO clients. These positions are located in Cincinnati, OH; Dallas, TX; or Minneapolis, MN. Our client offers a competitive salary, a $10,000 signing bonus, and a very generous relocation package. This is an incredible opportunity for candidate who are willing to move.
Operational execution of global multiservice clinical trials, including coordination of ...
Well established Biologics company seeking to overcome roadblocks to successful Oncology treatment, looking for PhD-level research scientist with 8+ years Translational Medicine experience. Will lead identification of Oncology biomarker activity and collaboration efforts towards companion diagnostics implementation. The person will actively enrich the cancer therapy pipeline through championing internal projects and support of collaborations with external partners.
Senior Principal Scientist will ...
Regulatory Medical Writer
Must have written all of the following: NDA submissions, Protocols, Narratives, Case Report Studies, and Inform Consent forms
Write clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, clinical development plans, previous human experience summaries, human pharmacology summaries, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical ...
Responsible for supporting the implementation and execution of clinical trials by performing specific project management tasks at country, regional and site level.
Ensure achievement of timelines and study deliverables with excellent quality and full compliance with international guidelines, local regulations and corporate policies and procedures.
Excellent verbal and written communication, problem solving skills and team orientation required. Project ...
Jan 24 -
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