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Online Resumes with "Clinical monitoring"
Clinical In-house Monitoring - 15 Years of Experience - Near 27514
Experienced monitor, study coordinator, study start-up specialist and medical researcher seeking position where knowledge of medical terminology, clinical trials experience, regulatory knowledge, organizational strengths, and strong people abilities can add to a company's overall quality and growth. Since 1998 I have been in Clinical Research. I have a strong background in clinical monitoring, study coordinating and quality...
Clinical Data Management - 9 Years of Experience - Near 01821
SUMMARY * I am certified-RAVE Study Builder- Certification Sponsored by Cognizant & Medidata USA. I have 12 years of experience in Project Management, Clinical Data Management, Technical Support and Team Management,Overall 10 years of progressive experience in Clinical Data Management domain from study start up till DBL activities. I am experienced with all aspects of data management including project management, edit check...
Tags for this Online Resume: Management, Data Management, Pharmaceutical Industry, Quality, Quality Control, Team Lead, Document Management, Audit, Training, Quality Assurance
Clinical Research Associate
Tags for this Online Resume: Clinical Research Associate, Clinical Research Associate, Clinical Trials Specialist, Clinical Trials Specialist, Clinical Monitoring Associate, Clinical Monitoring Associate, Clinical Trials Associate, Clinical Research Coordinator, In-house Clinical Research Associate, In-house Clinical Research Associate
Clinical Research Associate- 3 years Experience
To obtain a position as Clinical Research Associate (CRA) with a pharmaceutical / biotechnology firm where my knowledge and experience along with my strong technical and procedural skills in clinical monitoring can be utilized and challenged to meet the growing needs for clinical trials of new drugs and medical devices in multiple therapeutic areas. Also, to contribute to reducing the time it takes for a new drug to progres...
Clinical Monitoring Project Lead
Case Manager - 1 Years of Experience - Near 21224
SUMMARY: 30 years Clinical Research experience and home-based monitoring experience 12 years Oncology monitoring experience 12 years Pediatric Nurse experience 10 years Inform EDC experience and 6 months IMedidata experience 4 years as CRA trainer/mentor 3 years as Local Site Liaison/co-Clinical Monitoring Lead/Clinical Monitoring Lead THERAPEUTIC AREA EXPERIENCE: Oncology-12 years Non-Small Cell Lung-Phase III Colon-Phase ...
Tags for this Online Resume: Audit, Protocol, Clinical Research, Research, Nursing, Management, Monitoring, Therapy, Oncology, SAN (Storage Area Network)
Clinical Research - 8 Years of Experience - Near 60169
Professional Summary A certified professional Clinical Research with 4 years of experience in Clinical Research coordination and a year experience as Clinical Study Associate. Expertise in QC of documents, remote Monitoring and supporting the management by handling the tasks of multiple clinical research studies managing eTMF's & designing Clinical Portfolio's from Sponsor end. Expert in liaising between different departmen...
Tags for this Online Resume: Document Management, Monitoring - Remote and onsite, Clinical Research coordinator, Device trials, clinical Research, Project Management, QC and QA, Pharmacovigilance, Ethics and compliance, regulatory, Clinical study Associate, Multiple therapeutic areas experience, Phase 1-4 trials, Audits and Inspection readiness, Multiple software and application experience - Veeva VAULT , Impact , Quest , Sentinel,Tesla, EDC experience- RAVE Medidata, IRT system experience Clinpace , Endpoint
Clinical Research Professional
I am looking for a career opportunity in research or any science related field.
Ideal Companies: Any research company, FBI, CIA
Tags for this Online Resume: clinical, research, project management, biology, medical , science, monitoring, clinical trials, regulatory, quality assurance, laboratory
Clinical Research - 17 Years of Experience - Near 78745
Experienced with data entry and management of various EDC's to include IMPACT, Medidata/RAVE and CTMS * Therapeutic experience includes: Infectious Disease, Oncology, CNS, General Medicine, Mens Health, Cardiology and Dermatology * Received IAoCR (International Accreditation of Clinical Research) accreditation in February 2017 * Taught Continuing Education courses in Computer Skills at Austin Community College in 2000 - 200...
Tags for this Online Resume: Attention to Detail, Cardiology, Clinical Research, Communication Skills, Data Entry, Dermatology, Management, Medical, Oncology, Problem Solving, clinical, phase iv, Clinical monitoring, Phase I-IV, CRO, phase i, phase ii, clinical trials, pharmaceutical, cro, phase iii
Case Manager - 6 Years of Experience - Near 10031
Accomplishments are: - Ongoing training in Inpatient Utilization Procedures to audit and review medical records - Conduct on-site/off site review of medical records for quality of care and utilization. - Review process including DRG validation and Interqual criteria approval. - Utilized review criteria with the use of InterQual, 3M coding book and grouper, SIMS Plus. - Increased knowledge base on medical comorbidities in ad...
Tags for this Online Resume: Infrastructure, Support, Technical Support, Services, Public Health, Reviews, Quality, Acquired Immune Deficiency Syndrome (AIDS), physical therapist
Clinical Research Associate
Proficient in clinical nursing practice Excellent interpersonal relationship building abilities Strong verbal, written and computer skills Proven problem solving and decision making ability
Sr. Clinical Research Associate - 22 years Experience - remote - Austin, TX
A top-performing Senior Clinical Research Associate with extensive experience in clinical research, GCP, ICH, Regulatory, and clinical site management/monitoring. Solid background in critical care nursing for in-depth understanding of medical terminology for records review. Highly skilled in spearheading internal teams through clinical research and document management to ensure accuracy and adherence with study specific str...
Ideal Companies: Pharmaceutical, Biotech, Medical Device, CRO
Tags for this Online Resume: Clinical Research, Management, Protocol, Research, Documentation, Medical, Allergy, Monitoring, Reporting Tools, Cardiology, clinical, trial, gcp, protocol, pharmaceutical, regulatory, medical device, CNS, EDC, contract, remote, CRO
