We apologize for the inconvenience but the job you are looking for has been filled or it has been removed by the recruiter. For your reference, the original listing is shown at the bottom of this page.
Listed below are the top 10 out of 22 listings that are in the same industry and location as the job you were looking for. To see more than 10 listings, click here to search similar jobs in Houston, TX
Mudrock Research Geologist Houston, TXJob ID: U26208 Location:Houston, Texas, United States ShareRefer This Job To Friends Within Shell Projects & Technology, ...
STG International is seeking qualified candidates for the Psychiatrist position to work fulltime providing medical care to detainees in custody in support ...
Baylor College of Medicine HR Dept - Houston, TX US
Baylor College of Medicine is currently recruiting Research Nurses for Pediatrics Hematology & Oncology, 48340 and Pediatrics Hematology, position 213712. ...
Our WorldClass Research Institute Is Looking for a Scientific Leader Since its inception, The Methodist Hospital Research Institute (TMHRI) has challenged the ...
For your reference, we have included the original job posting below.
Clinical Research Associate (CRA)
Job Number:
26706558
Company Name:
Aerotek Scientific
Job Location:
Houston, TX US
Job Category:
Research
Clinical Research Associate (CRA)
Need 2 years field monitoring experience and 3 years oncology experience. RN or BS in life sciences. Will monitor up to 40-50 clinical pe:Monitors Clinical research phase I-IV trials activities at clinical study sites to assure compliance to GCP, SOPs, and study protocols. Review regulatory docs and prepares site visit reports. Essential Duties and Responsibilities:Successfully lead oncology study trials and site coordinators ensuring trial adheres to study protocols, qc, and timelines. Independently performs monitoring visits including pre-study, study site initiation, routine monitoring, and study site closure. Reviews monthly financials for variances and resolves ticipates in the development of draft protocol, draft CRFs, template informed consent and study docs. Ensure all documents remain current and valid and maintain internal trial master file to ensure inspection ticipate in the development of study specific sites coordinator and pharmacy training materials. Train site personnel on regs, policies procedures and forms. Run reports and review clinical data to identify issues and trends. Reviews monitoring visit reports and ensure compliance to protocol and timeliness. Take corrective action to resolve issues when erate and use metric tools to assure study is running per time-line and budget. Alert upper management and inter-face with sponsor company when needed regarding issues as imum Qualifications:BS degree in Health, Life Sciences or Scientific-related equivalent5 years of clinical research trial experience required2 years of field monitoring experience as a CRA (3 years total in Oncology) Category: Medical Sciences