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Online Resumes with "Electronic Data Capture"
Objective: To succeed in a company environment that fosters growth and excellence which provides me job satisfaction and self development and helps me achieve personal as well as organization goals. Aspirations: To be actively involved in a position where I can utilize the skills that I have acquired in my career and to excel in my field through hard work, skills and perseverance so to make an effective contribution to c...
Two years’ experience with clinical responsibilities for medical device companies with Class II devices – including an in-vitro molecular diagnostics device to detect infectious disease and a dermatological radiofrequency device that ablates nerves to reduce forehead wrinkles. Qualifications include leading a recruitment effort to secure 65 patients in 3 months across 5 sites, experience conducting and monitoring GCP phase ...
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
I would like to emphasize my enthusiasm about working in clinical research. I have had multiple family members and friends die from cancer, complications from diabetes, heart disease, addiction and mental illness. Please review my entire attached CV/Resume to see the bulk of my professional positions in research. I find clinical trials to be rewarding and purposeful. It is my hope to continue being part of the on-going disc...
PROFESSIONAL SUMMARY: A CRA with strong eye for detail and exceptional ability to interpret and follow instructions Possesses the ability to collect accurate data in line with client specifications excellent analytical and organizational skills knowledgeable in FDA regulations, GCP/ICH guidelines, seeking to join an organization that makes research subjects' safety its first priority. CORE QUALIFICATIONS: * Over 5 years exp...
Clinical Data Management Services, with extensive phase I-IV pharmaceutical experience in the following therapeutic areas: Dermatologic, Pathologic, Oncology, Ophthalmic, Infectious Diseases. Excellent analytical skills in data review and experience validation of data base design and study start up. Hands on knowledge of medical clinical research terminology and transcription, (EDC) Electronic Data Capture Experience.
A goal-driven dependable and dedicated management professional with over 12 years' solid experience in Clinical Data Management operations at a non-profit organization. Has extensive knowledge of GCP ICH and FDA regulatory requirements regarding management of clinical trials data. Expertise in data management practices for paper studies as well as electronic data capture systems. Has a proven ability to effectively communic...
Initialized Managed stable and equine healthcare, trained jumpers, started young horses under saddle. training under saddle and exercised horses of various disciplines to include: jumpers dressage polo and racing. Prepped and exhibited thoroughbred yearlings for sales pavilion. Assisted in endoscopy exams and radiological soundness exams.
Tags for this Online Resume: Scottsdale, Clinical Research, Compliance, Clinical Research Coordinator (CRC), Device Trials, Documentation, Clinical Trial, Medication Trials, Data collection, Microsoft, Electronic Data Capture (EDC), Regulatory submission
Clinical Research Associate with experience in both pharmaceutical and medical device clinical trials, possessing strong communication skills with sound analytical and problem solving techniques. Demonstrated ability to work independently and in a team environment. Experienced with electronic data capture (EDC) review, entry and query resolution. Skilled in performing clinical trials activities (including site selection, de...
Summary: Over 16 years managing clinical trials and data collection activities. Manage as Point of contact for sponsors, project teams, and investigational sites to facilitate clinical studies Phase I-IV. Responsible for the review and approval of case report forms, electronic data capture systems, review of protocols, implementing study procedure manuals, and monitoring plans. Additionally manage site selection, study exec...
SUMMARY Expert level Project Management, Data Management & Standards, Database Analysis and Application Design with Oracle Applications in the Pharmaceutical Industry. Extensive knowledge of Clinical Life Sciences Domain. Experience working for Sponsors, Biotech, Service Provider and CRO. Leadership capabilities to manage complex projects from project initiation to implementation. Delivery experience between the Business an...
Tags for this Online Resume: Data Management, Oracle Clinical, Structured Query Language, Applications, Pharmaceutical, Protocol, Consulting, Oracle Inform, Central Designer, Standards Project Management, Oracle Database, Clinical Information Systems, Electronic Data Capture (EDC), SQL Developer, SDTM Mapping, CDISC
SUMMARY OF EXPERIENCE Dedicated Clinical Research Associate with more than 10 years of experience in Clinical research. Broad background in clinical trials management of phase I/II/III/IV trials in Ophthalmology, Rheumatology/Immunology, and Endocrine including the implementation of study protocols, monitoring of sites and on-site data management and collection. Significant expertise in Ophthalmology Terminology, Treatments...