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Online Resumes with "Medidata Rave"

Senior Clinical Data Manager

Over 15 years of broad knowledge and experience in clinical database and project management activities in Roche pharmaceutical company. A result-oriented professional who effectively meet project commitment with strong interpersonal communications and ability to interface well with all level of organization. Mentors and support members of study management group. Highly skilled in EDC (Rave) and Oracle clinical data manageme...

Tags for this Online Resume: Medidata Rave, Oracle Clinical, Hyperion, Spotfire, Excel, Word

Senior Clinical Data Manager with 19 years of experience, Buffalo, NY - remote dm

Seasoned Clinical Data Manager with experience in complex projects and in managing multiple large, international clinical trials for Phases I - IV to GCP/ICH standards in biotech, pharmaceutical and non-profit venues. Ability to work within a complicated matrix environment while also independently self disciplined. Possesses solid project management skills with the ability to anticipate problems relating to projects and to ...

Tags for this Online Resume: EDC Leader, Medidata Rave, InForm, DM/Study Recovery Specialist, Mentor, Trainer

Clinical Data Manager with the Clinical Research expertise

I am a Clinical Research Associate with expertise in clinical study design, clinical database design, and managing multiple projects. I am exploring Clinical Data Management opportunities.

Tags for this Online Resume: Clinical Data Manager, Medidata Rave, CTMS, Clinical Data Associate, Clinical Research Associate

Featured Profile

clinical data coordinator-1.3 yrs of experience

• Independently and proactively perform all clinical data cleaning activities on assigned projects. • Thorough understanding of Clinical data management process. • Trained in Clinical Data Management systems Oracle Clinical (OC), Oracle Clinical-RDC (OC-RDC), Inform 4.3, MedidataRave.

Experienced Clinical Trial Manager located on the Central Coast of California

Tags for this Online Resume: California, Project Management , Oncology, Data Management, Project Oversight, Expert MS Office Applications User, OC RDC, iMedidata RAVE

Clinical In-house Monitoring - 13 Years of Experience - Near 08068

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

Tags for this Online Resume: Princeton, Study startup, In house CRA, CTA, Inform, Medidata Rave

Clinical Data Management - 7 Years of Experience

A Clinical Research Professional having around 7 plus years of experience in the industry. Have sound experience in Drug trials (pharmaceutical trails), phase I-IV studies with drug trials, Microbiology techniques, and Molecular diagnostics techniques. Having strong verbal and written communication skills, a great team player and fun to work with.

Tags for this Online Resume: Denver,, MEDIDATA RAVE, SPOTFIRE, EDC, Project management, risk based monitoring, centralised monitoring, QUERY MANAGEMENT, Research, Management, Medical, Database, Good Clinical Practices, ICH, Query, Support, Research, Management, Medical, Project Management, Query, Support, Test, User Acceptance Testing

Clinical Research - 4 Years of Experience - Near 60148

Tags for this Online Resume: Medidata RAVE, InForm, OC RDC, Serious adverse event (SAE) reconciliation, lab reconciliation, IVRS , , Microsoft Excel proficiency, Study lead, Client interaction

Developer - 7 Years of Experience

PROFESSIONAL SUMMARY * Over 9 years of Clinical SAS programming experience in a Pharmaceutical industry involving different Phases (I, II & III) of clinical trials. * Experienced in working closely with statisticians to provide SAS programming in analyzing clinical trials data and generating Statistical Analysis Files, Tables, Listings, Summaries and Graphs/Figures (TLFs) for the Integrated Summary of Safety (ISS) and Integ...

Tags for this Online Resume: Microsoft Windows, SAS, Structured Query Language, Unix, Microsoft Windows 7, Windows 7, PDF, Proc, Extensible Markup Language (XML), Microsoft Excel

Clinical Data Management - 14 Years of Experience - Near 28411

I am a Clinical Data Manager with 14 years experience in all aspects of clinical trial from early development to post approval. I am interested in using my extensive experience to join a Data Management group.

Tags for this Online Resume: Remote, Medidata Rave, Work from hom, Clinical Research, Early Development, Phase I-IV

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