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Online Resumes with "ICHGCP"

Clinical Project Lead

To actively work in collaboration with a cohesive clinical development team that values professionalism, process and results achieved in alignment with applicable SOPS, Working Practices, ICH/GCP and Regulations.

Clinical Research Coordinator

Profile: Certified Clinical Research Associate professional with extensive recent focus in CVS research and clinical trials. Combine resourcefulness and problem solving skills with clinical knowledge to consistently deliver improved research and production results. Team player dedicated to quality, continuous improvement and bottom-line objectives. QUALIFICATION HIGHLIGHTS • Knowledgeable in all areas of research including...

Ideal Companies: quintiles, Pfizer, Novartis, Aerotek, Abbott, J&J, Merck

Tags for this Online Resume: CRA program, clinical research coordinator

Sales Representative, NAPRx Certified, RMSR Certified

My objective is to achieve outstanding sales quotas and keep myself abreast of all current research and trends in the medical/pharmaceutical field. Skills such as understanding consumer/physician concerns, pharmacology, clinical paper, sales management, protocol, research, compliance, ICH/GCP, follow up, ability to grasp technical data and medical terminology are tools I possess to facilitate success in this industry. My ex...

Tags for this Online Resume: pharmaceutical, medical device, sales, public relations, fund raising, grant writing

Featured Profile

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

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 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 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