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Online Resumes with "IRB "



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

Statistical Programmer - 5 years Experience - US

Summary * Certified Base Programmer for SAS 9 with 5+ years of biostatistical programming experience in CRO, hospitals, pharmaceutical, and healthcare industries. * Involved in drug development process with experience in analyzing, reporting, and reviewing pre-clinical/clinical trial data. * Good understanding of FDA submission (IND, NDA) process, clinical protocols, CRFs, CDISC (SDTM, ADaM), 21 CFR Part 11, GCP, and IRB gu...

Tags for this Online Resume: SAS, Proc, Programming, Statistical Analysis, SAP, Research, Statistics, Structured Query Language, Management, Test

Administrative Services Manager

PROFESSIONAL SUMMARY Highly organized and detail oriented Administrative Assistant with more than 10 years' experience supplying thorough and organized administrative support to over 10 senior program officers. Professional background and expert knowledge of various computer technologies. Excellent at handling multiple projects with grace and accuracy. Resourceful, with extensive expertise and knowledge in office operations...

Tags for this Online Resume: Accounting, Administrative Assistant, Consulting, Credit Cards, Data Entry, HR, Human Resources, Logistics, Research, Research and Development

Clinical Research

PROFILE Decisive, action-oriented and results-focused professional offering more than 30 years of experience in the medical field with 23 years focused in clinical research. Thorough knowledge of Medicine. Ability to deal with the public in a professional, concerned manner and ability to convey a sense of confidence and trust to patients and work well with other health professionals. Knowledgeable of FDA, ICH and GCP guidel...

Tags for this Online Resume: ICH, EKG, Research, C Programming Language, Catalogs, Clinical Research, Hematology, Hepatitis, Hepatitis C, Scheduling

Clinical Regulatory Affairs - 6 Years of Experience - Near 92648

QUALIFICATIONS Document-Labeling Specialist, Nov.2015 - Feb.2016 Well-versed communicator, high organizational and analytical (Contract Position Only) abilities. Work well independently and as a member of a * Creation, Revision of CGL, pre-printed labels and IFU via team. Adept in SUSARs, IRB submissions, Sponsor redlining documents and SOP standards. monitoring, and CTMS files. Efficient at handling multiple regulatory doc...

Tags for this Online Resume: R programming, Word, Excel, Adobe Photoshop, Illustrator, google analytics, github, Adobe, Data Entry, Documentation, ISO

Scientist

SUMMARY Ph.D. in Chemistry with 20 years of academic experience in biomedical imaging and cancer research 5 years of business experience. * 17 years of leadership and management experience as principle investigator (PI) of biomedical research teams and multi-team consortium, including academia with private sector collaborations. Managed chemistry, medical physics, bioengineering and radiology laboratories. Served as PI in n...

Ideal Companies: cancer research, biomedical sciences, magnetic resonance

Tags for this Online Resume: Research, Applications, Biomedical Industry, Cancer, Chemistry, Clinical Research, COLI, Engineering, Imaging, Leadership

Analyst - 6 Years of Experience - Near 30058

Microsoft Word Excel PowerPoint Turnitin Safe- Assign Internet Explorer Blackboard FISS system Participant Recruitment tools Atlas.ti and IRB protocol

Tags for this Online Resume: Atlas, Benefits, Billing, Cancer, Coding, Data Analysis, Documentation, HIV, Management, Medicare, Research, Adjunct Instructor, Team Player, Organizational Skill

Quality Coordinator

Professional Summary: * Certified clinical research professional with nearly 10 years of clinical research experience in the medical device industry. I have a wide range of knowledge with site and study management having worked as an In-house/Field CRA, Lead CRA and Clinical Trial Assistant. * Conducting: Qualification, Initiation and Close-Out monitoring visits for pre and post-market trials. * Start-up activities for both...

Tags for this Online Resume: Documentation, Management, Data Management, Budgeting, Clinical Operations, Clinical Research, Collection, Compliance, Contract Negotiations, Distribution

Featured Profile

Regulatory Affairs and Compliance Expert

Detailed knowledge of substantial body of regulatory information, including but not limited to OHRP, FDA, HIPPA. Management and training of professional staff with leadership abilities that ensure communication and compliance from all entities. Skilled and well educated in performing audits, needs assessments and use of resources and appropriate resource management. Knowledge and experience with clinical, research report...

Ideal Companies: Research Institutions, Clinical Research

Tags for this Online Resume: Management, Policies and Procedures, Protocol, Research, Leadership, Compliance, Assessments, Health Insurance Portability And Accountability Act, Resource Management, Training

Clinical Research

PROFESSIONAL SUMMARY: Experienced Clinical Research Professional seeking career advancement with a CRO where I can make a positive contribution by utilizing my clinical research expertise. In-depth knowledge of clinical trial policies and procedures, study protocols, GCP guidelines, ICH guidelines, regulatory clinical trial documentation requirements, IRB documents submittal, sponsor electronic data capture systems for data...

Tags for this Online Resume: Chemotherapy, Clinical Research, Collection, Gastrointestinal, Oncology, PEDIATRIC, Protocol, Support

Clinical Research - 1 Years of Experience - Near 60091

Leverage Masters and Medical Degrees in clinical trials for new drugs and medical devices.

Tags for this Online Resume: AMICUS, Phlebotomy, Medical, Research, Cancer, clinical trials, regulatory, phase iii, phase ii, pharmaceutical, IRB, eCRF, Rave, ICF, Clinical Protocol, IB, Apheresis, Hematology, Leukemia Trials, GCP, Human Subject Protection, Medicine, HIPPA, Responsible Conduct of Research

Clinical Research

Tags for this Online Resume: Management, Audit, Budget Preparation, Budgeting, Cardiology, Data Management, Surgical, Clinical Research, Protocol, Research