Tags for this Online Resume:
Monitor, Data Management, Trial Master FIles, CRF, ICH-GCP, Electronic Data Capture, Clinical In-house Monitor
I am interested in a Project Manager or related position requiring multitasking and organizational skills to oversee multiple projects. I have eight years experience in the biotech/pharmaceutical industry. With the scientific, laboratory and management skills I have accrued over the years, I can perform tasks without supervision. I am looking for a position that allows further personal and professional growth.
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Global Clinical Trials Project Management, ICH, GCP, GLP knowledge, Research Associate , Independent Research , Preclinical trial management, Oncology/Chemotherapeutic drug discovery and development
Highly motivated and experienced biomedical professional with expert knowledge and proficiency in clinical research monitoring. A certified CRA. Hands-on experience in the clinical investigations of novel pharmacological products. Eager to translate expertise gained in research and monitoring to measurable success in the field clinical studies. A demonstrated record of academic achievement and recognition, accompanied by e...
Tags for this Online Resume:
Clinical Site Monitoring , Identification and interviewing of potential investigators, ICH GCP Training , Adverse Event Reporting, Study Planning Activities
Tags for this Online Resume:
Regulatory, Clinical Research, ICH GCP, Monitor, Electronic Data Capture, Project Manager
To find a job with a reputable pharmaceutical company that utilizes my experiences in clinical research study start up and ICH-GCP regulatory guidelines to provide process improvements and create a competitive advantage for the company.
Established reputation as a highly motivated and productive professional in the CRO/Pharmaceutical/Biotechnology industry. Able to quickly and thoroughly gain expertise in a particular field and integrate new information with the existing knowledge.
Capable of identifying and solving complex problems in creative and logical ways. Adept at combining critical solutions with imagination, innovation, and a sense of humor. ...
Ideal Companies: Stanford, Palo Alto Medical Foundation, Jazz
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All Database Knowledge, Excel, Microsof, ICH/GCP Compliant, Vendor Oversight, CTMS, Trial Master File, medical Device
To acquire a position as a Clinical Research coordinator in a pharmaceutical company or a CRO that will benefit from my skills, knowledge, experience and enthusiasm and that will give me an opportunity to learn and grow further.
To be responsible for the administration, initiation and monitoring of the Clinical research project in accordance with the FDA regulations and ICH-GCP guidelines.
Tags for this Online Resume:
clinical research assistant, data administrator, regulatory affairs assistant, CRA, Drug safety associate, Quality Assurance, clinical research associate
Looking for a challenging career in auditing in clinical research field.
Tags for this Online Resume:
GCP Auditor, ICH GCP, Quality Management System, Investigator Site Audits, Audits in MENA, Asia Pac, Vendor Audits
Tags for this Online Resume:
GCP, ICH, 21 CFR 50, 21 CFR 56, 21 CFR 312, 21 CFR 812, 45 CFR 46, Medical terminology, Data management, Project development, Site monitoring, CRA, CRC
