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Online Resumes with "ICH GCP"
Dedicated, outcome-focused, and skilled professional with broad-based perception and exceptional skills in clinical research, encompassing trial monitoring, site management, audits, and detailed record keeping. Interested in pursuing a challenging career as a Clinical Research Associate to utilize commendable multitasking proficiencies and technical documentation expertise. Commended for demonstrating a collaborative leader...
I offer a unique mixture of experience, knowledge and skills and am presently looking for new employment opportunities in Clinical Research where I can feel challenged and put all of who I am and what I have to offer to good use.
I'm an ambitiuos Clinical Research Professional contributing 8 years to the industry in project management, quality assurance/quality control, site coordination, internal clinical monitoring, and data collection. My healthcare background has rewarded me with skills in mulitiple thereapeutic areas consisting of: practice management, patient care, records system development, and team leadership.
To obtain a Clinical Research Position in the Minnesota Area.
Cover Letter Ignace Vallejo, MS. GCP and GMP QA Manager Certified Quality Auditor GMP; by CFPA. Certified Six Sigma “Black belt”. 525 Neptune Ave, Brooklyn, NY 11224. Apt 22 F Home # 718 946 0556. Mobile # 917 359 3028. email@example.com Good Clinical Practice (GCP). Audits were followed according to our SOPs and ICH GCP regulations and Guidelines. The vendor audits were preformed, as follows: • On Octo...
Current MPH Student in Epidemiology at Columbia University, PhD in Biological Sciences, experienced in Clinical Research Development & Management, Pharmacovigilance and Health Information Technology.
Skilled in the planning and implementation of clinical research projects in compliance with ICH-GCP, Regulatory Agencies, and company SOP. Study Start up expert. Proficient in Microsoft Office Applications, CTMS, IVRS/IWRS, INFORM, Medidata Rave. Therapeutic areas: Oncology, Cardiology, Neuroscience, Internal Medicine, including Diabetes. Participated in 3 FDA Submissions, FDA Inspection Readiness and TMF reconciliation
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...
Proactive, solution-driven professional that likes to perform assigned tasks with the best quality possible. With more than 10 years of experience in clinical research starting as Study coordinator, and being on different positions such as CRA, CRS and CPM, enjoying being part of, as well as managing, motivating and training a successful and productive team, through customer focus, team work and good relationships. Experie...
Clinical trial Research or Pharmacology Research
Experienced in SAS/BASE SAS/SQL, Assisted in CRF Annotation and edit check plans, experienced in offline listings, Good working knowledge on SDTM,CDISC Std. Good knowledge on Demography, concamitant medications, Medical History etc..