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Online Resumes with "DRA"
Registered Nurse - 8 Years of Experience - Near 18031
Tags for this Online Resume: drug safety, Argus, ARISg, MedDRA
Database Administrator
SUMMARY * 7+ years of experience as an Oracle Database Administrator on all versions of Oracle databases starting from 9i, 10g, 11g and 12c on different operating systems like Sun Solaris, Windows IBM AIX, HP-UX and Linux. * Experience in Oracle Flexible Architecture, I/O tuning, Capacity planning, space management, Memory Tuning, SQL Performance Tuning, Backup and Recovery, Optimization, Networking, script development and ...
Tags for this Online Resume: Oracle, Oracle Database Administration, Capacity Planning, Communication Skills, Configure, Data Modeling, Database, Database Design
RN Medical Coder - 18 years experience
Remote Medical Coder experienced in with ICD-9CM, ICD-10, WHODrug, WHO-ART, COSTART and MedDRA coding practices. Knowledge of diseases, drugs, dictionaries, and coding conventions. Multiple compound ownership interfacing with Clinical, Clinical Data Management and Clinical Safety to ensure appropriate coding for report analysis. Responsibilities include the daily running of studies, documentation of all procedures, regular...
Clinical In-house Monitoring - 6 Years of Experience - Near 07621
SUMMARY OF QUALIFICATIONS Pharmaceutical professional with 5+ years of clinical research experience in management and monitoring. Seeking new and exciting opportunities in new therapeutic areas to expand my expertise. Known for building strong relationships with clients and partnering with management teams to ensure quality services, compliance and efficiency. Manage Clinical Research, third party vendors, and clinical inst...
Tags for this Online Resume: Fraud, ICD-9, Insurance, Medical, Query, Management, Good Clinical Practices, ICH, Documentation, Clinical Research
Clinical Pharmacovigilance/Drug Safety
SUMMARY * Medical degree with over 25 year experience in clinical and drug safety surveillance setting within the pharmaceutical and Biopharmaceutical industry (Example: Amgen, Alza Corporation, Idec, Biogen Idec, Elan, Genentech, Roche, Sharing AG, Wyeth, Élan Pharmaceuticals, Actelion Pharmaceuticals) * Advance knowledge of US and international Safety regulations and Safety assessment of Marketed and Investigational drugs...
Tags for this Online Resume: Training, Data Entry, Coding, Policies and Procedures, Clinical Research, Data Management, Immunology, Management, Oncology, Query
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 - 10 Years of Experience - Near 20895
SUMMARY: International work experience in Pharmacovigilance, Clinical Trials, Pharmaceutical Sales and Regulatory Affairs encompassing Phase I experimental trials through post marketing safety reporting for the National Institutes of Health and for major pharmaceutical companies. Accomplishments include: Work Instruction Manual on Data Reconciliation for Astrazeneca. Led a team of six in writing the Work Instruction Manual ...
Tags for this Online Resume: Team Lead, MedDRA, RN, Acquired Immune Deficiency Syndrome (AIDS), oncology, Drug Safety Monitoring, Quality Assurance, Quality Control, Clinical Research Support, Data Management, Pharmacovigilance, FDA Reporting, IRB, International experience, Product Launch
Pharmacist - 14 Years of Experience - Near 19115
Experienced with Oracle Clinical, ClinTrial, ARGUS 7.0.7 databases, MedDRA 20.0, Who Drug coding systems, and EDC system.
Tags for this Online Resume: Management, Insurance, Managed Care, Coding, Data Entry, Data Management, Documentation, Pharmaceutical, Protocol, Regulatory Affairs
Medical Scientist - 5 Years of Experience - Near 07302
SUMMARY: * Proficient in ARGUS Data Safety submission and Narrative Writing * Thorough understanding and knowledge of MedDRA coding, pharmacovigilance practices for both Clinical Trial and Post marketing AE reporting * Well versed with GVP-ICH guidelines * ECFMG certified medical graduate with strong clinical knowledge * Self-driven, highly motivated medical professional with excellent leadership and organizational skills *...
Tags for this Online Resume: Drafting, Coding, narrative wrirting, ARGUS, MedDRA, Medical Reviewer, Drug Safety, labeling, ICSRs
Clinical Pharmacovigilance/Drug Safety - 2 Years of Experience - Near 29577
COVER LETTER: To whom it may concern: I am a Pharmacist with an equal combination of hospital and retail experience. I have seen many changes in healthcare over the past fifteen years of practice as well as the many pitfalls of a currently flailing economy. The aforementioned dynamics have affected the efficiency and safety of pharmacy. Of my prominent abilities are adapting to differing work environments and the staffing c...
Tags for this Online Resume: drug safety associate, Pharmacist, Medical communications , ICH, Argus, MeDRA, ICU, Chemotherapy, Complaints, Drug Information
Analysis of patient data through bedside care and pharmaceutical research for 35 years of exemplary work and experience
Objective * RN with 11 years of critical care experience with broad therapeutic clinical experience, expertise in development of processes for patient care, implementation and global training and project oversight. * Sixteen years of clinical research experience, which includes nine years in Drug Safety/Pharmacovigilance experience analyzing subject data. * Quality focused Data Management Associate Director of Clinical List...
Tags for this Online Resume: Business Development, Database, Development Activities, Infrastructure, Gastrointestinal, Intensive Care, Oracle, Critical Care, clinical, research, clinical trials, cro, pharmaceutical, Clinical
General - 7 Years of Experience
KEY QUALIFICATIONS: * COMPLAINTS & TECHNICAL SUPPORT SPECIALIST WITH 5+ YEARS OF PHARMACEUTICAL AND MEDICAL DEVICE INDUSTRY experience * 5+ years of experience with product complaints including experience with Global Customer Complaints (GCC), adverse events, and auditing of complaint records * Excellent knowledge of quality standards and regulations: FDA QSR 21 CFR 803 & 820, ISO Standards 9001 / 13485 / 14971, MDD 93/42/E...
Tags for this Online Resume: Complaints, Good Clinical Practices, Medical, Pharmaceutical, Support, Technical Support, Clinical Research, Project Management, Project Manager, Research
