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Online Resumes with "ICH "



Clinical Trial Specialist / CRA _ Home based

Achieve the successful of clinical trial and ensure the subject safety and the high data quality by working closely with each clinical site and ensure that all the tasks are being conducted in accordance with the clinical trial protocol , ICH GCP guidelines and local regulations.

Clinical Trials Manager

Dear Hiring Manager, I am interested in exploring career opportunities with your company and have therefore enclosed my resume for your review. This position seems ideal for my experience, education, skills, and career interests. I am eager to contribute my enthusiasm and teamwork to your organization. My professional goal is to enhance my research development and senior leadership experience. I believe that I could...

Clinical Research Coordinator New Orleans, LA

Monitor assigned clinical trials, interact with all different department such as (monitoring resources, project manager, quality assurance and data management). Conduct site visits (initiation, monitoring and close out). Ensure the adherence to FDA, ICH & GCP regulations. Instruct the site staff in their roles and responsibilities in conducting clinical trials. Ensure the completion and collection of regulatory document...

Tags for this Online Resume: Clinical Research Coordinator, Data Manager, Medical Assistant

Featured Profile

Clinical Trials Associate

Michelle Straka, BSHS, CPT 1163 Portsmouth Circle Medina, Ohio 44256 Cellular: (216) 337-2007 Home: (330) 722-2165 Email: dodgestealthrt1994@yahoo.com Linkedin account: http://www.linkedin.com/pub/michelle-straka/1b/964/aa2 Objective Obtain the position of Clinical Research Associate to further advance monitoring career. About four years additional experience in research as a study coordinator, regulatory coordina...

Senior Research Nurse Coordinator

I'm a competent, organized, detailed oriented and efficient Clinical Research Nurse Professional with 10 years experience and proven administrative skills. Experience includes OB/GYN, Vascular Surgery, Podiatric and Ophthalmology Reserach. Excellent communication skills and proficient in time management and problem solving abilities. Knowledge of GCP and ICH guidelines, regulatory requirements, and the clinical trial process.

Senior Clinical Research Associates

I want to ensure that sites that I monitor are completed accurately according to Code of Federal Regulations and GCP/ICH.

Sr. Director/Director Clinical Quality Assurance and Compliance

Over 19 years of Regulatory / Clinical Quality Assurance & Compliance / Auditing experience. Maintain an excellent knowledge base of all applicable Guidelines, FDA Regulations as well as best practices. I have prior interaction with the FDA, and EMEA/MHRA authorities, leading to successful outcomes. I am considered to be a strategic leader and planner effective in a team environment and customer service focused, with exc...

Tags for this Online Resume: Clinical Quality Assurance, Compliance, Auditor, GCP, Quality Systems, Director

Expert Biostatistician

Statistical analysis in pharmaceutical industry

Tags for this Online Resume: Biostatistics, SAP, FDA, NDA, ICH/GCP, SAS

Clinical Research Associate - 10 plus years Dallas, Field Application Specialis/Fiels Service Engineer - 5 years plus, San Francisco & Dallas

I am a strong self-starter with over 10 years’ monitoring experience with monitoring phase I to phase IV for pharmaceutical companies, biotech companies and CROs. I also have over 5 years’ experience as a Field Application Specialist with a biotech company which is a similar position as a Pre-sales and Medical Device Expert at a biotechnology company. I work well independently or in a team environment. I am presently lookin...

Tags for this Online Resume: Dallas/Ft. Worth, TX, Clinical Research Associate, Regional Clinical Research Associate, GCP, ICH, FDA, Code of Federal Regulations, Clinical Research Studies, Therapeutic Areas

Clinical Research Associate and QA with 1 year experience and M.Sc. in Science with 10 years' experience

To get a position as a Clinical Research Professional and involve in Canada pharmaceutical industry.

Tags for this Online Resume: ICH/GCP guidelines, FDA requirements , Design and revised protocol, Standard Operating Procedure , Case Report Form (CRF), Informed Consent Form (ICF), Adverse Events (AE) and Serious Adverse Events (SAE) , Data Managemnet, MS office, Phlebotomy, CPR, Recruit subjects

Senior Clinical Research Associatec

To be involved in clinical research

Tags for this Online Resume: clinical research associate, clinical team leader, senior clinical research associate, monitoring , FDA regulations, Phase 1- IV studies, site selection to site closeout, maintain GCP ICH compliance, GCP ICH compliance