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Online Resumes with "ICF "
Clinical Pharmacovigilance/Drug Safety - 2 Years of Experience - Near 27713
Tags for this Online Resume: FDAguidelines, Medical writer, ICH GCP, Essential documents, Regulatory guidelines, E3 guidelines, Investigator brochure, ICF
Case Manager - 2 Years of Experience - Near 03253
Active case manager working in the insurance industry for an MCO of state Medicaid program is looking to expand her experience to include the hospital-based and/or medical office-based case manager role.
Ideal Companies: Dartmouth Hitchcock Medical Center, Concord Hospital, Catholic Medical Center
Tags for this Online Resume: Educator, MSN, Rehab, Med-Surg, NCQA, Adult, Pediatric, Patient Care, Nursing, Home Care, Support, Technical Support, ICU, Critical Care, FACETS, CCMS, BSN, diligent, organized, prioritize, patient education, assessment/reassessment, strategize, utilize strengths, overcome barriers, goal achievement, utilize resources, interdisciplinary, teamwork
Clinical Research Associate
SUMMARY: To apply my knowledge of FDA Good Clinical Practice guidelines/ICH guidelines, extensive site/field Clinical Director, Site Lead Study Management, in addition to my experience with various therapeutic areas of medicine, to a position as a Clinical Research Associate. AREAS OF EXPERTISE * Management * Interview candidates and either make a selection decision or recommend individuals for hire. * Able to manage multip...
Tags for this Online Resume: Clinical Research, Research, Accounting, Acquired Immune Deficiency Syndrome (AIDS), Advertising, Amazon Elastic MapReduce, Audit, Basic First Aid, BLS, Budgeting
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 Regional Monitoring - 10 Years of Experience - Near 20912
20/20, Addis Ababa University (CRO), Addis Ababa, Ethiopia, March 2005 to July 2006 Senior Clinical Research Associate - Opthalmology Studies, National Blindness, Low-Vision & Trachoma * Oversaw $3.5M study across 14 regional states to explore blindness, low-vision, and trachoma demonstrated sharp organizational skills in managing team of clinical data managers verifying data, and performing systematic networking of databas...
Tags for this Online Resume: Clinical Research, Research, Protocol, Collection, Critical Care - Neurology, Management, Neurology, Oncology, Quality, Quality Assurance
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
Communications Teacher - 14 Years of Experience - Near 07080
Profile I am a Certified Master Spiritual Coach, Certified Transformational & Wellness Coach - ICF Approved and also a Certified NLP - Master Practitioner. I always had an intense zeal for understanding people and their behavior. Being Intrigue and Self Determined to explore human lives has brought me a long way in understanding the different aspects of a human life. Over 14 years of professional experience across various i...
Tags for this Online Resume: Coaching, Planning, Management, Process Improvements, Product Launch, Quality, Quality Assurance, Assessments, LMS, Customer Service
Certified Clinical Research Coordinator - 13 Years of Experience - Near 34202
Seasoned Certified Clinical Research Coordinator with 13 years' experience as a CRC, including experience in marketing, advertising, and regulatory document completion and submission. Completed my duties with great attention to detail, compassion, professionalism, confidentiality, and care. Seeking a position in healthcare/clinical research/pharmaceutical industry that will allow me to continue to exercise these skills and ...
Tags for this Online Resume: Clinical Research, Research, Good Clinical Practices, Protocol, Advertising, Documentation, Marketing Management, NPI, Training, Accounts Payable, clinical, trial, phase, gcp, protocol, pharmaceutical, GCP, IRB, CRF, ich, AE, SAE, SUSAR, Inclusion and Exclusion Criteria, ECG, Biological, PK, PG, Substudy, ICF, EDC, Rater, concomitant medications, IP, IP accountability, regulatory documents, master file
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
General - 10 Years of Experience - Near 38703
To assist dually diagnosed individuals with mental health and substance abuse issues to return to their communities as viable, productive, citizens. Also assist people with developmental disabilities in becoming active in their community through therapies, counseling, active treatment, supportive interventions, and social services. 20+ years in the field of Developmental Disabilities, inclusive of nine years of Managing an ...
Tags for this Online Resume: Computer Aided Software Engineering, Management, human services
Regional Home-Based CRA
Tags for this Online Resume: oncology, phase, clinical, trial, gcp, protocol, pharmaceutical, Cardiovascular, CRO, Neurology, Bone, immunotherapy, monitoring, Initiation, close-out, Remote, query, onsite, SOP, ICH, GCP, investigator, IRB, sponsor, CTMS, CNS, Endocrinology, Haematology, ICF, Informed Consent, EDC, SDV, InFORM, MediData Rave, eTrial, eDiary, MedWatch, Adverse Event AE, SAE, 1572 Statement of Investigator, IB, Trip Report
