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Online Resumes with "Clinical Research Studies "
Clinical Research Scientist
I would like to obtain a Clinical Scientist Position in the pharmaceutical industry. I am currently finishing my second year of an industry-based clinical research/drug development fellowship program with United Therapeutics (UT) in collaboration with the University of North Carolina (UNC). My training and experience has primarily been focused on early stage clinical development, particularly in Phase I clinical pharmacolo...
Tags for this Online Resume: clinical scientist, clinical pharmacology, oncology, drug development, clinical trial leader, medical writing
Quality Coordinator - 16 Years of Experience - Near 75211
I'm a Clinical Research Regulatory Specialist who has over 17 years experience in monitoring & assuring FDA regulatory compliance of documents for clinical research studies.
Clinical Research - 3 Years of Experience - Near 07205
Objective To obtain a rewarding position in the pharmaceutical industry allowing me to utilize my laboratory, research, and interpersonal communication skills to be a positive contributor to successful drug development and an asset to my employer. I am a fast learner, dedicated and conciencious worker with a passion for scientific research..
Tags for this Online Resume: clinical study coordination, subject recruitment, inclusion and exclusion criteria for clinical study, •drug accountability and reconciliation, •source document review and update, assist with TMFs, Pre-Clinical research studies, blood collection, processing and shippment from sunjects
Research
To obtain a challenging position within the Pharmaceutical industry or medical devices industry that will allow me to use my experience to play a key role in Clinical Research studies and projects, and/or product development with medical devices.
Tags for this Online Resume: Clinical Pathology, laboratory method development, IQ, OQ, PQ, instrumentation, validation of medical devices, Regulatory, GLP, GCP, IRB, TMF, Project Manager, Documentation Specialist, Scientist, Archives
Clinical Research, Study Assistant, Data Verification, GLP, Administrative, SOP, Quality Control, Shipping
To provide excellent administrative and study data support in a Biotech Research setting.
Professional Researcher - 10 Years Experience
PhD with documented success and experience in a diverse range of fields including academia, pharmaceuticals, and the medical device industry. Excellent writing, presentation and data analyses skills. Strong interpersonal skills with a remarkable ability to communicate scientific information to a diverse audience. Motivated by systems to improve human health and patient care.
Ideal Companies: Stryker, Johnson and Johnson, Glaxo Smith Kline
Tags for this Online Resume: Research, Infectious Diseases, Statistics, Medical Devices, Spine, Orthopedics, Sales, Pennsylvania, Clinical Research Manager, Biology, Immunological Assays, Client Relations, Social Media, Large-Scale Studies, Vaccines, Market Analysis, Event Planning, Sales Cycle Management, Data Analyses, qPCR, Genome Sequencing, Global Research, Journal Publications, Published Writer, Media Relations, Presenatations, Team Leadership
Certified Sleep Technologist/Clinical Coordinator//Registered Medical Assistant, Atlanta, GA
I am currently attending Strayer University for Healthcare Administration, BA degree program. My career goals and objectives are to become a Healthcare Director. My pass and future experiences in the medical field industry show clinical, administrative and managerial experience in all areas of expertise. I also work well in either a team or individual environment. My career path is full of compassion for people who are in n...
Tags for this Online Resume: Certified Sleep Technologist, Registered Medical Assistant, Clinical Research/Study Coordinator, Neurobehavior Counselor, Managed/oversee offsite facility, CPAP Therapist
Clinical Research - 20 Years of Experience - Near 60601
-Participate in development of new intramural clinical research studies, both for solid tumors and hematology/oncology, reviewed all new protocols, supervised designing case report forms for the new protocols for the solid tumors and hematology/oncology. -Work with the multiple investigators on developing and implementing new intramural oncology protocols and supervised accomplishments with all protocols' requirements. ...
Clinical Research - 8 Years of Experience - Near 60169
Professional Summary A certified professional Clinical Research with 4 years of experience in Clinical Research coordination and a year experience as Clinical Study Associate. Expertise in QC of documents, remote Monitoring and supporting the management by handling the tasks of multiple clinical research studies managing eTMF's & designing Clinical Portfolio's from Sponsor end. Expert in liaising between different departmen...
Tags for this Online Resume: Document Management, Monitoring - Remote and onsite, Clinical Research coordinator, Device trials, clinical Research, Project Management, QC and QA, Pharmacovigilance, Ethics and compliance, regulatory, Clinical study Associate, Multiple therapeutic areas experience, Phase 1-4 trials, Audits and Inspection readiness, Multiple software and application experience - Veeva VAULT , Impact , Quest , Sentinel,Tesla, EDC experience- RAVE Medidata, IRT system experience Clinpace , Endpoint
Clinical Research - 12 Years of Experience - Near 78254
SUMMARY OF QUALIFICATIONS * Managed Phase I -IV and observational Clinical Research Trials for HIV/AIDS, HIV Vaccine trials, HIV and Hepatitis, Infectious Diseases, Hyperlipidemia, Diabetes, Renal CKD, Secondary Hyperparathyroidism, Vitamin D Deficiency, Diabetic Nephropathy, Allergies, Asthma, and Immunology, Hepatic therapeutical area, from HBV, HCV, Fatty Liver, Cirrhosis in the Liver, medical devices. * As an inhouse mo...
Tags for this Online Resume: PEDIATRIC, Pharmaceutical, Surgical, C Programming Language, Data Entry, Hepatitis, Hepatitis C, Research, Therapy, Cardiovascular
Clinical Research - 3 Years of Experience - Near 02478
Summary: MS in Clinical Investigation with 3+ years of experience as Clinical research assistant cum coordinator seeking a preferably full time position in Clinical Research fields as Clinical Trial Associate / Project Management. Offering combination of strong background in biological sciences (specialization in Oncology, Molecular biology) as well as deep understanding and knowledge of ICH-GCP & FDA regulations. Demonstra...
Tags for this Online Resume: Clinical Research, Documentation, Research, Advertising, Audit, Budgetary, Data Entry, Data Management, Filing, Gastroenterology, Recruting, IRB admministration, regulatory, phase ii, clinical trials, ICH-E6 GCP and GLP, HIPAA compliance
Clinical Research - 10 Years of Experience - Near 30067
SUMMARY OF EXPERIENCE: Ensuring quality and integrity in the conduct of clinical research studies to comply with standard operational procedures as defined by GCP and FDA regulations. Manage the conduct of clinical trials within the United States and International markets. Responsible for the delivery of high quality data considering resources, time and cost. Therapeutic areas include: * ONCOLOGY * INFECTIOUS DISEASE * CNS ...
Tags for this Online Resume: Clinical Research, Research, Pharmaceutical, phase i, phase iv, phase ii, phase iii, pharmaceutical, regulatory, cro, clinical trials, research, clinical
