CV, Curriculum Vitae and Online Resumes Search

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Online Resumes with "study protocols"

Toxicologist - 19 Years of Experience - Near 60134

SUMMARY I am a highly motivated individual that is driven to succeed, with proven strategic decision making ability and acute attention to detail, underscored by a career highlighted with numerous promotions and high level positions in successful industry and contract research laboratory (CRO) environments in an international setting. I have had great success at aligning cross-functional research and development teams to su...

Tags for this Online Resume: Analytical Chemistry, Applications, Attention to Detail, Compliance, Data Analysis, Data Management, Due Diligence, Good Clinical Practices, protocol, pharmaceutical, ich, GLP

Research Assistant - 15 Years of Experience - Near 20144

To secure a position where my vast experience in biomedical facility regulations, development of animal study protocol, technical skills, animal health and welfare will be of benefit.

Ideal Companies: Pfizer, Convance

Tags for this Online Resume: Animal Research Technician, Doctor of Veterinary Medicine, Documentation, Quality Assurance, Test, bedding, Good Laboratory Practices, Health and Welfare, Research, Water Supply, clinical, research, pharmaceutical, regulatory, cro, clinical trials, phase i, phase ii, phase iv, phase iii

Clinical Regional Monitoring - 20 Years of Experience - Near 18929

Seeking an opportunity with a Pharmaceutical, Biotechnology company or CRO as a Senior Lead Clinical Research Associate, Lead CRA, CRA Manager/Trainer (Mentor) and/or CRO Oversight Monitor to employ my 27 years of clinical research monitoring, management skills and CRA mentoring as well as19 years of Respiratory/Pulmonary and Cardiopulmonary critical care clinical medicine. Clinical Research Experience: Projects/Therapeutic...

Tags for this Online Resume: Pharmaceutical, Clinical Research, Research, Rheumatology, Biomedical Industry, Pharmaceutical Industry, Cardiology, Critical Care - Neurology, Critical Care - Respiratory, Neurology, oncology, clinical, phase, gcp, protocol, trial, ich

SAS Programmer - 3 Years of Experience - Near 76010

A certified SAS programmer with Master's degree in Biostatistics is seeking a position in which the statistical analysis knowledge and SAS programming skills can be utilized. CORE QUALIFICATION * More than 4 years' experience in analyzing data for both pharmaceutical study and public health research. * Experiences in survey data collection, cleaning and mining. * Proficient in statistical methods: linear regression, ANOVA, ...

Tags for this Online Resume: SAS, Structured Query Language, Active Directory Application Mode (ADAM), Base SAS, Data Analysis, Database, Macro (Predefined Code)

Biologist - 20 Years of Experience - Near 94806

Career Summary * Lab Manager with over 25 years of optimizing efficiencies. * Able to coordinate initiatives (both scientific and administrative) within research laboratories strives to propel professionalism while minimizing the efforts produced within the workplace. * Adept at supporting and collaborating with other team members to implement the most appropriate policies, procedures, and protocols for assignments. AREAS O...

Tags for this Online Resume: Administrative Assistant, Critical Care - Neurology, Neurology, Research, Radiation, Complaints, Water Supply, Adobe, Adobe Acrobat, Adobe Illustrator

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 Research - 6 Years of Experience - Near 80918

Pursuing a challenging career in an organization where I can apply my talents and education in a medical/scientific-related field. Qualification Highlights Proficient use of Databases: iMedidata RAVE, RTOG, GOG, Inform, Oncore, CTSU, SWOG, Clincapture. Oversee RNs are strictly following X-Chart requirements of study protocols. Reviews Expectancy Reports of all associates in our department to ensure data timelines are met. R...

Tags for this Online Resume: Clinical Research, Research

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

Director of Quality - 20 Years of Experience - Near 91709

SUMMARY OF QUALIFICATIONS * Over twenty years of experience managing regulatory affairs (RA)/quality assurance (QA), quality control (QC)/research & development (R&D) departments in pharmaceutical, medical device and dietary supplement manufacturing industries. Implemented Quality Management Systems meeting domestic and international regulatory requirements and ISO registration. Reviewed pre-clinical, clinical and pharmacok...

Ideal Companies: Pharmaceutical, Medical Device, Biomedical

Tags for this Online Resume: Quality, Quality Assurance, Quality Control, Manufacturing, Regulatory Affairs, Microbiological Testing, Test, ISO, Pharmaceutical, ADA

Clinical Research - 20 Years of Experience - Near 32828

My career objective is to become a part of your Organization and to apply my experience and knowledge during the conduct of clinical trials, with emphasis on safety, efficacy in accordance to ICH-GCP, FDA and study protocol guidelines. Further, I will always strive to accomplish efficiency and savings for clients, by developing effective monitoring tools

Tags for this Online Resume: Microsoft-Office, ICH-GCP, FDA-guidelines, CTMS, EDC, RAVE, Monitoring, Clinical trials, Cardiovascular, Management, Auditing

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 SAS Programming

SUMMARY * A Certified SAS Programmer with over six years of working experience in SAS applications for Clinical Research and Analysis. * Experienced working with Pharmaceutical companies and CROs. * In depth experience and knowledge in various SAS products such as BASE /SAS, SAS /MACROS, SAS/STAT, SAS/ACCESS, SAS/SQL in Windows and UNIX environments. * Worked extensively by using base/SAS, SAS/macro, SAS procedures (proc so...

Ideal Companies: Mrs.

Tags for this Online Resume: Cancer, Protocol, SAP, SAS, Oncology, PDF, Proc, Programming, Statistical Analysis, Structured Query Language