CV, Curriculum Vitae and Online Resumes Search

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Online Resumes with "Clinical Research Professional"

Clinical Research - 3 Years of Experience

Summary * Highly qualified clinical research professional with over 17 years' experience, including Phase I-IV domestic and international studies (including EU, Eastern EU, South America, Asia, and Canada) in a wide range of therapeutic areas. * Experienced in all stages of study development from start up to close out with ability to view study progress by each data point or from a more global prospective. * Skilled at effe...

Tags for this Online Resume: Clinical Research, Oncology, PEDIATRIC

Clinical Research - 20 Years of Experience - Near 33467

SUMMARY A highly experienced and innovative clinical research professional with over 25 years of progressive and comprehensive experience as a study coordinator, SMO assistant site director and associate director successful management of multiple projects, mega trials and teams simultaneously while meeting or exceeding specified timelines in a remote environment. Most recently created and trained a dedicated Informed Consen...

Tags for this Online Resume: Management, Inventory, Pathology, Research, Accounting, Clinical Research, Documentation, General Accounting, Health Insurance Portability And Accountability Act, ICH

Clinical Research - 15 Years of Experience

SUMMARY A highly experienced Clinical Research professional with considerable experience in all stages of clinical trial processes, gained within the Biotech, CRO and Pharmaceutical environments. Key experiences areas: CNS- Psychiatric/Migraine/Alzheimer/Seizure/Movement Disorders Epilepsy, Cardiovascular- Statins, Type 1 & 2 Diabetes, Infectious Disease- HIV, AIDS, Autoimmune (NMO), Medical Device-stents, valves, glucomete...

Tags for this Online Resume: Clinical Programs, Clinical Research, Research, Protocol, Cardiovascular, Management, COPD, Distribution, Oncology, Vendor Management

Experienced Clinical Research Associate

As an experienced clinical research professional, I am looking to use my degree in Clinical Trials Research and 10+ years of experience as a successful leader at the department and study levels, to enhance my knowledge and skill set as an in-house CRA or to expand my career as a Clinical Research Associate, responsible for monitoring investigative sites.

Clinical Research - 16 Years of Experience - Near 94547

SUMMARY of QUALIFICATIONS 16 years of experience as a Clinical Research professional in Biotech and Pharmaceutical industries. Well-rounded skill, as a CRA in Clinical Operations processes, Clinical Development, Regulatory, TMF and Data Management. Skilled in data audit/review Study start up, Study conduct, Vendor management, and Site monitoring activities extensive knowledge of GCP-ICH, GLP, GMP guidelines familiar with Ex...

Tags for this Online Resume: Protocol, Assessments, Audit, Clinical Research, Documentation, Pediatrics, Research, Clinical Management, Distribution, oncology, phase, trial, clinical, protocol, pharmaceutical, gcp, ich

Clinical Research - 20 Years of Experience - Near 27517

SUMMARY Clinical Research Professional with more than 20 years experience in Phase II-IV clinical site management, regulatory compliance and monitor training for major pharmaceutical companies. Demonstrated expertise in electronic systems including CTMS, EDC, IVRS, CRF design, query management and corporate communications. Proven success in all aspects of clinical trials from study start up through close out in phase IIb-IV...

Tags for this Online Resume: Protocol, Clinical Research, Research, Audit, Training, Clinical Research Associate

Clinical Research - 16 Years of Experience - Near 07052

SUMMARY: Clinical research professional with experience conducting and managing sponsor related clinical trials Phases I-IV following GCP and ICH requirements and guidelines. Clinical trial experience in various indications including Oncology (Solid Tumors, Prostate, Lymphoma and Renal Cell Carcinoma) and Cardiovascular (myocardial infarction, acute ischemic stroke, and Venous Thrombo-Embolism). Strong team player experienc...

Tags for this Online Resume: Management, Billing, Direct Patient Care, Integrate, Inventory, Inventory management, Medical, Medical Billing

Senior Clinical Research Associate - 20 Years of Experience - Near 92596

COVER LETTER: Dear Hiring Manager: My goal is to obtain a position where I can utilize my clinical research experience, sound knowledge of Good Clinical Practice (GCP), good judgment and analytical skills, attention to detail, creativity, international experience, interpersonal skills and reliability that are well suited to the needs of the Company and the Senior Clinical Research Associate position. My sound academic train...

Tags for this Online Resume: Analytical Skills, Clinical Research, Problem Solving, Problem Solving Skills, Public Health, Reliability, Research, Regional Clinical Research Associate, Data Queries, Audit, Clinical Trial, GCP, Protocol, Data Management, ICH, Phases I-IV

Clinical Research - 1 Years of Experience - Near M1W 2T1

Foreign-trained medical doctor and clinical research professional with CRA Professional Development Clinical Site Monitoring & ICH GCP Training. Experienced in clinical study files review to ensure accuracy of all the documented data including ME & AEs. Comprehensive knowledge of clinical research methodology and proficient in Phase I-IV clinical studies and ICF processing and study protocols. Excellent time management and ...

Tags for this Online Resume: Toronto, Canada, Strong Clinical Trials & Medical Management background, Detail Oriented, Data Review, Clinical Trials Supervision, Team player, Quick Learner, Certified CR Professional with Medical Background, Compliance, Documentation, clinical, research, phase i, phase ii, clinical trials, phase iv, pharmaceutical, cro

Clinical Regional Monitoring - 3 Years of Experience - Near 0000

PROFESSIONAL SUMMARY Clinical Research Professional with various project experience from concept to development. Talents include in-depth knowledge of ICH guidelines SAE reporting and GCP auditing. Integral team-player with excellent communication skills CORE QUALIFICATIONS * Patient Recruitment & Screening * Detailed Documentation * Serious Adverse Event Reporting * Communicating with IRB for study proposal, approval and u...

Tags for this Online Resume: Clinical Research, Data Entry, Research, Audit, Communication Skills, Compliance, Documentation, Excellent Communication Skills, Good Clinical Practices, ICH

Clinical Research - 5 Years of Experience - Near 20720

A Clinical Research Professional position with a pharmaceutical/biotechnology firm or Research Organization where I can utilize my medical and clinical research training and experience along with my strong technical and procedural skills in clinical studies and data management to work as part of a team to reduce the time it takes for a new drug to go from IND through NDA to the market by adherence to GCP and FDA rules and ...

Tags for this Online Resume: phase iii, clinical, phase i, research, pharmaceutical, cro, regulatory, clinical trials, phase ii, phase iv