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Online Resumes with "Regulatory Documents"
High energy and friendly office professional with high aptitude for making friends and providing aid. Customer service expert with dedication to being a team player
Seasoned Clinical Research Professional with 10+ years experience in Clinical Research, including, CRA, Lead CRA, and Project Management duties. THerapeutic areas include oncology, endocrine/metabolism, and CNS.
A job where our can continue to use my extensive and professional environmental experience with an organization that works with the Air Force.
Ideal Companies: SAIC
I am looking for a permanent/full time position as a business analyst, QA analyst, assistant project manager, or IT work lead.
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.
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.
Provide quality manuscripts, regulatory documents, and medical information documents in support of the development of innovative pharmaceutical products.
I have an eclectic background with very strong focus on customer service. With my most recent company, I have risen through the ranks from novice airline sales representative to air and hotel Quality Management in less than two years. Before that I worked hard and learned quickly, progressing from a pharmaceutical research office's temporary receptionist to the company's youngest Senior Research Coordinator. My strong wor...
I am seeking a regulatory documentation position where I can expand my experience and skills.
I am seeking to end my present consulting status and return to an in-house position where continuity of projects is more realized. I have over 15 years experience writing regulatory medical documents that comprise CFR21 356h NDA/BLAs and eCTDs deliverables to the FDA/EU/Canadian regulatory authorities. I have written approximately 85 CSRs and can confidently say that ~40 of these were NCEs, early phase I/II and some pha...
Tags for this Online Resume: Regulatory Medical Writer Manager level
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.
Elaboration of regulations, policies and perform risk management for health products recalls, market withdrawals and safety alerts, nationally and internationally.
Ideal Companies: U.S.Food and Drug Administration (FDA)