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Online Resumes with "Adverse Event AE"
Clinical Research Associate and QA with 1 year experience and M.Sc. in Science with 10 years' experience
To get a position as a Clinical Research Professional and involve in Canada pharmaceutical industry.
Tags for this Online Resume: ICH/GCP guidelines, FDA requirements , Design and revised protocol, Standard Operating Procedure , Case Report Form (CRF), Informed Consent Form (ICF), Adverse Events (AE) and Serious Adverse Events (SAE) , Data Managemnet, MS office, Phlebotomy, CPR, Recruit subjects
Medical reviewer, Chicago
CAREER SUMMARY Self-motivated, detail-oriented reliable drug safety physician with 8-year-experience in pharm/biotech industry with good knowledge of global pharmacovigilance (PV) regulations, clinical medicine and bio-medical research; led and conducted single case (ICSR) medical review in therapeutic areas (TA) oncology, medical assessments, proactive signal detection and aggregate safety analysis ...
Featured Profile
Clinical Research - 15 Years of Experience - Near 90001
I am seeking a position in Clinical Trial Management or as a Project Manager per my previous US and international experience.
Ideal Companies: Pharmaceutical or Biotech
Tags for this Online Resume:
Oncology, Orthopedics, Surgical, Clinical Research, Management, Medical, Medical Affairs, Diabetes, Cardiovascular, Women's Health, Clinical Trial Management, Regulatory, Medical Writing, Microsoft, CTMS
Clinical Pharmacovigilance/Drug Safety - 4 Years of Experience - Near L6Y 0K6
SKILL SUMMARY * Medical Physician with over 7 years of experience in world class hospital and multinational Contract research organization (CRO) highly result oriented with successful completion of multiple clinical research projects, managed and reported Serious Adverse Events (SAE) and Adverse Events (AE) to various regulatory bodies. Hand on experience on project review and overall project management. * Proven track reco...
Tags for this Online Resume:
Cardiopulmonary resuscitation (CPR), Clinical Research, Compliance, Hindi Language, ICU, Inventory, Leadership, Logistics
Biostatatician - 6 Years of Experience - Near 46802
Professional Summary: * SAS Certified Programmer with around 6 years of experience in clinical trials data analysis and reporting in Health care and Pharmaceutical fields. * Well-versed with clinical data analysis: analyzing clinical data, creating tables, listing and generating reports and graphs as per requirements, specifications and Statistical Analysis Plan (SAP). Experienced with SAS procedures such as Proc Format, Pr...
Tags for this Online Resume:
Protocol, SAP, Clarify, Data Analysis, Documentation, ETL, Extensible Markup Language (XML), Extract Transform Load Tools
Clinical Research Associate
SUMMARY: To apply my knowledge of FDA Good Clinical Practice guidelines/ICH guidelines, extensive site/field Clinical Director, Site Lead Study Management, in addition to my experience with various therapeutic areas of medicine, to a position as a Clinical Research Associate. AREAS OF EXPERTISE * Management * Interview candidates and either make a selection decision or recommend individuals for hire. * Able to manage multip...
Tags for this Online Resume:
Clinical Research, Research, Accounting, Acquired Immune Deficiency Syndrome (AIDS), Advertising, Amazon Elastic MapReduce, Audit, Basic First Aid, BLS, Budgeting
Clinical Research - 10 Years of Experience - Near 18901
Summary: * Several years of clinical experience in the industry with excellent knowledge of drug development in different therapeutic areas including oncology, immunology, vaccines, metabolism and biosimilars. Solid clinical practice experience. * Many years of Drug Safety, pharmacovigilance, risk management and epidemiology experience * Experience interfacing with health authorities (worldwide), institutional review boards...
Tags for this Online Resume:
Oncology, Protocol, Regulatory Affairs, Risk Assessment, Management, Risk Management, Risk Management Activities, Complaints, Documentation, Hematology, Medical Affairs, Clinical Development
Quality Assurance Specialist - 10 Years of Experience - Near 08817
Project Summary: ARISg is a Drug Safety System which provides all the functionality required to manage adverse event reporting and adverse reaction requirements of different authorities around the world, from case entry to automatic generation of submission ready adverse event (AE) reports including CIOMS I, Med Watch 3500A and many more. ARISg is an automated distributed system. In this system data would transfer to variou...
Tags for this Online Resume:
Test, Regression Testing, Management, QTP, Test Scripts, Business Requirements, Framework, Coding, Functional Testing, Java Programming Language
Programmer Analyst - 8 Years of Experience - Near 22042
PROFESSIONAL SUMMARY * Over 8 years of experience in Information Technology field with strong emphasis in SAS Application Analyst/ Programmer with 3+ years of hands on experience and professional experience in Clinical Trial projects and also worked as Application Analyst in the CROs, Healthcare and Pharmaceutical industries. * Experience in analyzing and coordinating clinical data, generating detail summary reports and dat...
Tags for this Online Resume:
Management, Oracle, Oracle 9i, Information Technology, Process Improvements, Coding, Health Care Industry, HyperText Markup Language, Manufacturing, sql, SAS analyst
Regional Home-Based CRA
Tags for this Online Resume:
oncology, phase, clinical, trial, gcp, protocol, pharmaceutical, Cardiovascular, CRO, Neurology, Bone, immunotherapy, monitoring, Initiation, close-out, Remote, query, onsite, SOP, ICH, GCP, investigator, IRB, sponsor, CTMS, CNS, Endocrinology, Haematology, ICF, Informed Consent, EDC, SDV, InFORM, MediData Rave, eTrial, eDiary, MedWatch, Adverse Event AE, SAE, 1572 Statement of Investigator, IB, Trip Report
Contract Medical Writer
Summary Work Experience: Strong background in medical writing and biotechnology product and services development, with a solid publication record in the peer-reviewed medical literature in addition to biotechnology analyst articles-an unusual combination of medical writing expertise, analytical skills, data analysis, management experience, and medical knowledge. Participate in pre-clinical, clinical, and commercial research...
Tags for this Online Resume:
Business Development, Cancer, Clinical Research, Medical Writer, regulatory science, biologics, drugs, medical device
Clinical Research - 15 Years of Experience - Near 90001
I am seeking a position in Clinical Trial Management or as a Project Manager per my previous US and international experience.
Ideal Companies: Pharmaceutical or Biotech
Tags for this Online Resume: Oncology, Orthopedics, Surgical, Clinical Research, Management, Medical, Medical Affairs, Diabetes, Cardiovascular, Women's Health, Clinical Trial Management, Regulatory, Medical Writing, Microsoft, CTMS
