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Online Resumes with "Crf"
Clinical Research Associate
Working currently as Senior CRA and Business Development Manager in UK. Want to relocate to US to be closer to my family. Great knowledge in Scandinavian and European authorities such as MHRA,MREC and R&D.
Ideal Companies: Biotech, pharma, university, hospital
Tags for this Online Resume: Oncology, Infection, Respiratory, ICH GCP, regulatory, CRF, Protocol, monitoring, pain, close out
Experienced Data Coordinator Relocating to Dallas, Texas
I am looking for a company where I can add to my extensive list of Data Coordinator skills as well as share my skills with others. Working for a company which fosters the expansion of knowledge, is constantly growing and supports its employees is very important to me.
Tags for this Online Resume: SAS, eDM, Oracle Clinical, DMP Composition, CRF Completion Guidelines Composition, External Data Reconciliation, Multi-tasker
Application Support
Tags for this Online Resume: clinical data, data coordinator, CRF Developer, data review, information manager, QA/AC
Clinical Research Project Manager, Charlotte North Carolina
To acquire a mid level to managerial administrative position within the clinical research therapeutic field
Tags for this Online Resume: regulatory, data manager, project manager, quality assurance, auditor, monitoring, electronic data capture, GCP, research, eCRF, CCRP, human subject's protection, source documentation, study start up, primary outcome analysis
Clinical Data Manager, 7 years experience
I am currently looking for work as a Clinical Data Associate, Data Manager or Data Coordinator. During my 7 years in the biotech industry, I have worked on all aspects of Data Management from the Data Entry process to the creation and implementation of the study documentation to the CRF and Database creation and implementation of Edit checks. I also now have a site perspective since my last experience was working directly w...
Tags for this Online Resume: Data Management, pharmaceutical, clinical research, oncology
Clinical Research Associate
SUMMARY OF QUALIFICATIONS • Foreign graduate Medical Doctor and licensed RN with more than 22 years of clinical and research experience. US citizen. Fluent in English, Russian and Romanian • Extensive training in Good Clinical Practices, ICH Guidelines, SOPs through various Sponsors • In depth therapeutic and protocol knowledge as per Sponsor’s assignment. Excellent organizational and problem-solving skills.
Ideal Companies: Biotech companies
Tags for this Online Resume: research associate, biotech, CRA, Las Vegas, pharmaceutical, health
Registered Nurse - Drug Safety Associate,Coder, Product Surveillance/Product Safety
I am seeking for a stable and well established company that is growing. Also,what I am looking for in a new job is for employers that care about their employees and acknowleges them for their good hard work. I would also hope that good training is provided so that the individual such as myself can be productive for the company and contribute towards it's success rate. I would also hope that it was a warm welcoming environm...
Ideal Companies: Cephalon Pharmaceutical, Teva Pharmaceutical, Azur Pharmaceutical, GlaxoSmithKline, United BioSource
Tags for this Online Resume: Registered Nurse, Drug Safety Associate, Coder, Safety Surveillance, Adverse Event Coordinator
Clinical In-house Monitoring, Clinical Data Management, Central New Jersey
Tags for this Online Resume: Monitor, Data Management, Trial Master FIles, CRF, ICH-GCP, Electronic Data Capture, Clinical In-house Monitor
Certified Clinical Research Coordinator
To obtain a position as a clinical research coordinator
Ideal Companies: Genentech
Tags for this Online Resume: GCP's, CRF's, Resolve queries, Consent study participants
Clinical Data Manager - India - 7 Years Exp. - Very Very Quick Learner
Overall 6.9 years of experience in Clinical Data Management. Broad experience in Data Management which includes Data Validation, Query Initiation, Client Interaction (Face-To-Face or WebEX), Reviewing of important Documents (Protocol, eCRF, Electronic Specifications, Data Entry Guidelines etc). Highly efficient and skilled at providing coaching and guidance to Internal and External Clients.Very Fluent in English.Excellent i...
Clinical Research Associate
Seeking to utilize my professional expertise in a clinical trial setting supporting good clinical practices as a clinical research associate. I am motivated to promote my efficient skills in being a quick learner, multi-tasker, detail oriented, proactive, and having great organization and communication skills. I uphold high quality standards and able to respond to rapidly changing priorities.
Tags for this Online Resume: clinical , research , medical , monitoring, devices, CRF
