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Online Resumes with "ICH GCP"

Research Director- 18 yeras if experience managing sites

I have over 18 years of professional experience established in clinical research. As my resume indicates, I have experience in all aspects of clinical trials. I recently worked as the Director of Clinical Operations in a clinical site where I performed all aspects of clinical trials and the daily operation including problem solving. I have successfully managed the quality assurance department and acted as a trainer for t...

Clinical Research Professional - Specializing in Study Start Up

I am ready to take my career to the next level. I am a Clinical Research professional specializing in Study Start Up with experoence in: ICFs, Site Regulatory Packages, ICH-GCP, Feasibility and Contract Negotiation.

Tags for this Online Resume: ICH-GCP, Study Start Up, Informed Consent, Contract Site Agreements, Feasibility , Regulatory Documents

Featured Profile

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

Project Manager, Clinical Trials

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.

Tags for this Online Resume: Global Clinical Trials Project Management, ICH, GCP, GLP knowledge, Research Associate , Independent Research , Preclinical trial management, Oncology/Chemotherapeutic drug discovery and development

Clinical Research Associate

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

Sr. Clinical Research Associate

Tags for this Online Resume: Regulatory, Clinical Research, ICH GCP, Monitor, Electronic Data Capture, Project Manager

Start-up Specialist

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.

Clinical Research Professional, San Francisco Bay Area

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

Tags for this Online Resume: All Database Knowledge, Excel, Microsof, ICH/GCP Compliant, Vendor Oversight, CTMS, Trial Master File, medical Device

Clinical Research Associate, Boston

 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

Clinical Quality Assurance

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

Clinical Research Professional, Charlotte, ICH/GCP/FDA Trained

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