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Online Resumes with "consents"
Clinical Research Coordinator or Monitor
I am very enthusiastic about beginning a career in clinical research. As you can see I have no direct experience in this field, however, my father was in a clinical trial study at Emory University for his prostrate cancer. I followed his participation in the study and was involved in his care during this time. In addition, as a home health care nurse, I treated several patients that were also involved in clinical trials in ...
Tags for this Online Resume: CRC, Phase II, Registered Nurse, CRA, Clinical Research Associate, Clinical Trials
Experienced Research Professional seeks CRA position!
Passionate, hard-working, intelligent, leader, compassionate, organized
Ideal Companies: I would enjoy working with any CRO or Sponsor who values and rewards excellence and a strong work ethic from their employees.
Tags for this Online Resume: Clinical Research Associate, CRA, Regulatory, Monitor, Auditor, GCPs
Enthusiastic New Graduate
Offering: Practical experience and education in social science research, effective communication and demonstrated diligence, interest in healthcare and human services. Long term goal is a graduate degree in health education and promotion.
Tags for this Online Resume: research assistant, case manager, psychology, non-profit
Goal-oriented, meticulous, highly organized
not only exceptional technical competency but also superior analysis, problem-solving abilities, leadership, communication and team member experience.
Ideal Companies: Companies that have more than 50 employees and been in business for awhile.
Tags for this Online Resume: sales and marketing, customer service, regulatory affair, research and development, management, sales, development
QA Lead Investigator, Process Specialist (Process Validation)
Over five years of diverse validation experience in the Pharmaceutical industry. Enthusiastic, ingenious, and results oriented professional. Highly effective in teamwork environment. Oriented towards resolution of problems. Knowledge of principal and supplemental FDA Regulatory Guidelines like: Solid Dosage Blend Uniformity, Dissolution Guideline, Stability Guidelines, cGMP, Conformance Standards, SUPAC and SOP’s. Expe...
Sr. Clinical research Associate/ Director of clinical research
Can undertake most of the tasks and works independently. Very much focussed on the timelines and quite goal tending. Willing to help others in their prioritized tasks. Excellent planning, design and implementation. Highly experienced in writing reports and data analyses.
Ideal Companies: Pharmaceutical industries, Biotech companies, Research institutes, hospitals and for profit mid to large companies.
Tags for this Online Resume: Director of clinical research, Manager of drug safety, Senior clinical research associate, Regional clinical research associate
Regulatory Affairs Assistant, Durham/RTP
Seeking a full-time position utilizing my written,organization skills in a government, health care, clinical research setting with an emphasis on regulatory affairs submissions, informed consent, and FDA requirements
Medical Statistician-15 years experience-Gloucester Health Authority, Dept of Environment,
My objective is to support all health professionals in understand clinical research from the correct methodology to data collection to data analysis. Can support in writing case report form, questionnaire design,inform consent form
Lead Project Manager- Clinical Trials
Proven expertise in managing teams, streamline project paths encompassing an understanding of scientific data, analysis and interpretation of results, clinical developability and commercial viability of projects.
Ideal Companies: Vertex Pharmaceuticals, Amgen Inc., Takeda Pharmaceuticals
I am MD by background with more than 5 years of clinical research experience
I am looking for a challenging job in a team-oriented environment.
Ideal Companies: Allergan, Genentech, Ista, Santen
RN Case Manager, 12 years in the Healthcare industry
12 years experience in healthcare, most recently in Clinical Case Management and Quality Control. Four years practicing in the case management and quality control industry combined with five years of a clinical background, provide the skills necessary to assist organizations in administration and management in quality cost effective health care. Increasing responsibilities in the areas of direct patient care, asses...
Tags for this Online Resume: RN, Case Manager, Triage RN, Telecommute RN, RN, CCM, RN, RUGS
Senior/ Lead Clinical Reseach Associate - over 15 years experience monitoring, site management, medical record review, training/mentoring junior CRAs. database locks. regional clinical team leader
My goal is to secure a regional, home-based position in which I can use my knowledge of all phases of clinical research to develop tools to collect data (CRFs/edit checks; to verify the data (site management/monitoring), clean data (database locks)and to insure patient safety by assuring all AE/SAEs are reported, protcols and infomed consent are IRBs approved and adherence to all ICH guidelines and regulations.
Tags for this Online Resume: Lead CRA, Data Manager, Sr. CRA, Regional CRA
