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Online Resumes with "ICH GCP Guidelines "

Master of Pharmacy with 7+ yrs exp

Looking for QC/QA/Clincal research/Formulation/Sales job at entry level.

Ideal Companies: Pharmaceutical, Heallthcare, Clinical research, Pharmaceutical Sales


Registered Nurse - 25 years experience CRA one year experience

Clinical Research Associate. Also RN with 25 years plus experience. Looking for position with pharmacology or hospital of clinical research.

Tags for this Online Resume: Clinical Research Associate, Registered Nurse, Ability to travel, Ability to work at home, FDA/ICH GCP Guidelines, MS Work knowledge

Featured Profile

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

Drug Safety / Pharmacovigilance - RTP, NC

Dynamic, enthusiastic, and performance-driven Doctor of veterinary medicine intent on transferring 10 years of knowledge and experience in a clinical setting to a challenging career working in the Pharmaceutical or Contract Research Organization industry with a progressive company offering opportunities for growth and advancement. Outstanding team player and communicator with highly detailed documentation skills seeking t...

Tags for this Online Resume: Medical terminology, ICH/GCP guidelines, DIsease states, Pharmacology, Customer service, Medical writing

Clinical Research, Raleigh

To Obtain a position congruent with my education and level of experience in the Clinical Research field.

Tags for this Online Resume: Clinical Research Associate, Clinical Research Associate, ICH-GCP Guidelines, ICH-GCP Guidelines, Source Verification, Source Verification, Regulatory Document Maintenance, Regulatory Document Maintenance, Site Initiation Visits, Site Initiation Visits, Drug Accountability, Drug Accountability

Clinical Research 14 years experience

My objective is to use my extensive knowledge of clinical research, FDA, ICH, and GCP guidelines to obtain a career in the Pharmaceutical/Biotech industry.

Tags for this Online Resume: Clinical Reserach, IRB, Human Subject Protection, Audit, Monitor

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 Associate

Michelle Straka, BSHS, CPT 1163 Portsmouth Circle Medina, Ohio 44256 Cellular: (216) 337-2007 Home: (330) 722-2165 Email: Linkedin account: 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...

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

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

Clinical Research Associate

To obtain a Clinical Research Position in the Minnesota Area.

Tags for this Online Resume: Knowledge of 21 CFR, Quality System Regulation (QSR), Medical Device Reporting, Regulatory Compliance , Regulatory Submissions , ICH GCP Guidelines