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Online Resumes with "Regulatory documents"
Manager preclinical studies, prepare clinical regulatory documents IRB/ICB submissions IND applications
My career objectives are to focus on clinical coordinator, study manager, quality assurance, and regulatory. For the last six years I have worked in preclinical testing drugs, getting them from pre-IND to IND submission and into the clinic. The next logical career move is to work in clinical.
Ideal Companies: All companies are ideal.
Tags for this Online Resume: Clinical Coordinator, Study Manager, Regulatory, Generate Protocols, Generate Case Report Forms, Preclinical study manager, Clinical, Stereotactic Neurosurgery, Tumor Models, Subcontracts, Office Manager
Clinical Research Coordinator
To gain experience in all aspects of clinical trials while having an immediate impact on the progression of medicine.
Tags for this Online Resume: clinical research, regulatory documents, regulatory affairs, clinical research associate, clinical research coordinator, laboratory
Patient Access Director, Health Care Director and Administrator, Rancho Cucamonga
Seeking an Executive Level position responsible for innovative organization management, administrative surveillance, staff development, regulatory documentation, consulting, leadership training and program development in the private and/or public sector where my 30 years of administrative, managerial, technology and teaching skills can be utilized.
Clinical Research Associate
SUMMARY OF QUALIFICATIONS • Foreign graduate Medical Doctor and licensed RN with more than 22 years of clinical and research experience. US citizen. Fluent in English, Russian and Romanian • Extensive training in Good Clinical Practices, ICH Guidelines, SOPs through various Sponsors • In depth therapeutic and protocol knowledge as per Sponsor’s assignment. Excellent organizational and problem-solving skills.
Ideal Companies: Biotech companies
Tags for this Online Resume: research associate, biotech, CRA, Las Vegas, pharmaceutical, health
Regional Clinical Monitoring, Kansas City, MO
To monitor clinical trials of all phases using extensive knowledge of drug development and regulatory processes. Experience: - study site selection and set up – preparation of pre-study regulatory documentation - preparation of site monitoring reports in accordance with specific timelines - follow-up and resolution of sites issues - identifies and assists sites with DCF resolution - maintains regular contact with ...
Tags for this Online Resume: Clinical Trial Manger, Clinical Research Associate (CRA), Medical Writer (MW), Project Manager, Clinical Research Scientist, Clinical Operation
Regulatory Specialist II, Tampa, Florida
I have over 10 years of experience working as a Regulatory Specialist. I love all aspects of clinical research. I enjoy reading a protocol and learn how that particular study may help certain group of people. My goal is to find a position where I be responsible for providing guidance to study personnel regarding regulatory and IRB issues, Good Clinical Practices, and FDA Regulations. To be in charge with maintaining and r...
Tags for this Online Resume: Clinical Research, Regulatory Specialist II, Pharmaceutical Clinical Trials, CRA
Registered Nurse - Drug Safety Associate,Coder, Product Surveillance/Product Safety
I am seeking for a stable and well established company that is growing. Also,what I am looking for in a new job is for employers that care about their employees and acknowleges them for their good hard work. I would also hope that good training is provided so that the individual such as myself can be productive for the company and contribute towards it's success rate. I would also hope that it was a warm welcoming environm...
Ideal Companies: Cephalon Pharmaceutical, Teva Pharmaceutical, Azur Pharmaceutical, GlaxoSmithKline, United BioSource
Tags for this Online Resume: Registered Nurse, Drug Safety Associate, Coder, Safety Surveillance, Adverse Event Coordinator
entry level healthcare administration
To utilize my skills and knowledge towards a challenging career in Industry that offers security and Professional growth while being innovative and driven.
Tags for this Online Resume: Regulatory documentation, Quality Assurance documentation, administrative procedures, good communication skills, fluency in 4 languages
Registered Nurse, Clinical Research Coordinator, pharmaceutical trials, consultant, experienced
As my career goals are on target with my education and expertise, I am now seeking a non-traditional nursing role where my experience and education have provided me with knowledge in a wide range of areas with many prospects that require skills I have acquired over a long career. I am ready to move in a new direction using my passion for research, law, creativity, travel, information technology, consulting, advising and the...
Ideal Companies: Stanford, Amgen
Tags for this Online Resume: Registered Nurse, Research, Medical Records Reviewer, BSN, Coordinator , Consultant, Sales, Entrepreneur, Clinical Research Coordinator
Clinical Research Professional - Specializing in Study Start Up
I am ready to take my career to the next level. I am a Clinical Research professional specializing in Study Start Up with experoence in: ICFs, Site Regulatory Packages, ICH-GCP, Feasibility and Contract Negotiation.
Tags for this Online Resume: ICH-GCP, Study Start Up, Informed Consent, Contract Site Agreements, Feasibility , Regulatory Documents
