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Online Resumes with "ICH GCP Guidelines"



Clinical Research - 10 Years of Experience - Near 11801

Cover Letter Rupal brahmbhatt Respected sir/madam ,, My self Rupal Patel Brahmbhatt. I was working at Synchron Research Services a leading CRO of India. I have been the part of this organization from when it was established, and still I was working with the same organization from 12 years. I have been a part of more than 700 projects as well as clinical studies including USFDA submission projects. I have face the US...

Tags for this Online Resume: MS office, GCP, SOP, CRA, ICF, CRC

Clinical Research Associate - Entry level - Waterloo

Driven, dynamic, and detail oriented. Trained in ICH/GCP guidelines to monitor clinical trial processes. Actively seeking an entry level CRA position within clinical trial programs.

Tags for this Online Resume: ICH/GCP, Clinical Research, SOPs, Case Report Forms, Microsoft Office Suite, Phases I - IV trials, Recruitment

Clinical Research

Experienced Clinical Research Associate seeking a challenging and rewarding Clinical Research Associate (CRA) position that will utilize my clinical site monitoring and general management skills and experience to coordinate, monitor and manage all aspects of clinical trials in accordance with the ICH-GCP guidelines, FDA regulations, standard operating procedures and study protocol.

Clinical Research - 15 Years of Experience

Focused on obtaining a position as a Clinical Research Associate. Detail oriented with the ability to plan organize coordinate and manage projects according to priorities. Ongoing and consistent promotion of team work efforts. Excellent Communication and Interpersonal skills. Excellent oral and written communication skills with the ability to communicate effectively with medical personnel. Quick learner with the ability to ...

Tags for this Online Resume: Documentation, Management, Cardiovascular, Cardiology, Clinical Research, Distribution, Good Clinical Practices, Research

Clinical In-house Monitoring - 4 Years of Experience

Seeking a position in a globally focused organization that will utilize my qualifications while offering several opportunities to integrate personal enrichment with professional goals.

Tags for this Online Resume: Clinical Research, ICH GCP Guidelines, Schedule Y, eCRF, EC Submission, Site coordination, Inspection, Project Coordination

Clinical Data Management - 9 Years of Experience - Near 01821

SUMMARY * I am certified-RAVE Study Builder- Certification Sponsored by Cognizant & Medidata USA. I have 12 years of experience in Project Management, Clinical Data Management, Technical Support and Team Management,Overall 10 years of progressive experience in Clinical Data Management domain from study start up till DBL activities. I am experienced with all aspects of data management including project management, edit check...

Tags for this Online Resume: Management, Data Management, Pharmaceutical Industry, Quality, Quality Control, Team Lead, Document Management, Audit, Training, Quality Assurance

Clinical Research with 7 years of experience in medical field for different positions - Near M1G 3S4

Actively looking for an opportunity to work as a Clinical Research Coordinator. Recently completed the Placement as a Clinical Research Trainee from Toronto Rehabilitation Institute (UHN), Toronto on Sep 30, 2016. Key-Skills: * Possesses Post graduate Diploma in Clinical Research with medical background and experience of working in health field for more than 7 years * Well-developed time management skills and excellent atte...

Tags for this Online Resume: Data Entry, Medical, Health Awareness, Training, Cardiopulmonary resuscitation (CPR), Clinical Research, Phlebotomy, ICH-GCP Guidelines, Pharmaceutical Industry, Patient Recruitement, Clinical Trial

Clinical Research - 2 Years of Experience - Near 77449

HIGHLIGHTS OF QUALIFICATIONS: * RN with close to 2-years experience in clinical trials monitoring * Knowledgeable of clinical trial procedures and approval processes. * In-depth knowledge of ICH GCP guidelines and FDA regulations * Conversant with Design and Review of case report forms (CRF) * Conversant with Site Monitoring visits (PSVs, SIVs, IMVs and COVs) to meet study expectations. * Clinical and post-marketing safety ...

Tags for this Online Resume: Direct Patient Care, DRESSING CHANGES, Medical, Patient Care, Suctioning, Surgical, Wound Care, Acquired Immune Deficiency Syndrome (AIDS), HIV, Monitoring

Scientist - 15 Years of Experience - Near 10583

Summary: Molecular Biologist with expertise in highly driven research environment experience ranging from writing grant proposal, MTAs with pharmaceutical companies, planning experiments, wet bench laboratory techniques, data collection, analysis, writing articles for publication in journals, preparation and presentation at National and International meetings to teaching and training students and fellows and supervising tec...

Tags for this Online Resume: Oncology, Research, Cancer, Pharmaceutical, Translation research, Medical writing, liaison, Management, Senior scientist, Clinical scientist, CRA, scientist, oncology, cancer research, medical liaison

Medical Scientist - 13 Years of Experience - Near 21136

HIGHLIGHTS OF QUALIFICATIONS: * 2+ years of clinical research monitoring experience and 25+ years pre-clinical experience * Knowledge of clinical trial procedures and approval processes. * In-depth knowledge of ICH GCP guidelines * Knowledge of FDA regulations * Knowledge of clinical trials for investigative biomedical and pharmaceutical studies. * Good working knowledge of Pharmacology, Epidemiology, Biology, Chemistry, Ph...

Tags for this Online Resume: Cancer, Leadership, Medical, Patient Care, Quality, Quality Assurance, Quality Control, Trauma, Troubleshooting, Phlebotomy

Medical & Clinical Laboratory Technician - 6 Years of Experience - Near 60706

SUMMARY OF QUALIFICATIONS * BA and Masters Degree in Bioengineering and Biotechnology from Poland * Motivated team player, detail oriented, result focused with excellent time management and people skills * Proficient in MS-Office (Word, Excel, ) and the internet * Strong knowledge of anatomy and physiology, medical terminology, ICH GCP guidelines * Proven ability to work efficiently and effectively under pressure * Versatil...

Tags for this Online Resume: Administrative Assistant, Documentation, Patient Care, Scheduling, Therapy, Management, Pathology, Protocol, Satellites, Polish/English

Clinical Regional Monitoring - 10 Years of Experience - Near 20912

20/20, Addis Ababa University (CRO), Addis Ababa, Ethiopia, March 2005 to July 2006 Senior Clinical Research Associate - Opthalmology Studies, National Blindness, Low-Vision & Trachoma * Oversaw $3.5M study across 14 regional states to explore blindness, low-vision, and trachoma demonstrated sharp organizational skills in managing team of clinical data managers verifying data, and performing systematic networking of databas...

Tags for this Online Resume: Clinical Research, Research, Protocol, Collection, Critical Care - Neurology, Management, Neurology, Oncology, Quality, Quality Assurance