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Online Resumes with "health authorities"
Innovative Professional
Skillful professional with highly developed communication skills and years of progressive success assisting organizations in achieving optimal operating and profit-generating status. Innovative, resourceful and inventive thought leader, adept at taking quantifiable risks to leverage strategic advantages and eclipse competition. Excellent understanding of changing business conditions to customize and integrate leading edge s...
Ideal Companies: Medium to large health or social services organization
Tags for this Online Resume: Executive Director, CEO
Pharmacovigilance Specilaist
Pharmacist with 16 years of experience in various roles ranging from clinical setting to regulatory activities
Ideal Companies: pharmaceutical
Tags for this Online Resume: pharmacovigilance, regulatory operations, regulatory submissions, drug safety, regulatory affairs
Clinical Safety physician 10 years experience all therapeutic areas, all phases of development I-IV, communicating with Health Authorities
Ideal job is to manager other safety physicians producing documents for Health Authorities
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
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
Senior Director, Chicago
To obtain a leadership position for regulatory affairs expertise in the pharmaceutical/biotech industry
Tags for this Online Resume: regulatory affairs, pharmaceutical, biotechnology, clinical , manufacturing
Regional Aboriginal Patient Advocate 5 years experience with 2.5 years as Interim and/or Acting Director for hospital based and regional focus program with the Winnipeg Regional Health Authority
My goal is to work in a leadership role which will enhance health care to Aboriginal peoples. My preferrence is to work with the federal government to achieve this using my expertise in Aboriginal health and Social Work values.
Diversified, what a great portfolio!
Self starter with intelligence and determination to find the answers and complete the tasks
Ideal Companies: Blue Cross, Blue Shield, University of Chicago, Rush St. Luke's, workers' compensation carrier
Tags for this Online Resume: compliance, regulatory, paralegal, insurance, training
Featured Profile
Principal Scientist/Analytical Project leader
Seek position in R&D as a analytical development team leader handling multiple projects, coordinate project activities with various departments (quality assurance, Reg. CMC, Clinical Manufacturing Unit, Drug supply management, technical operations and outside contract laboratories. Direct analytical method development and oversee analytical development for the formulation development at contract labs
Tags for this Online Resume:
Publications, Diagnostics, Pharmaceutical, Research, Research and Development, Support, Technical Support, Audit, Compliance, Medical
Energetic, results-oriented individual with established credibility and respect at FDA and EMA. An extraordinary record which includes the lead and approval on New Drug Applications (NDA) and Marketing Authorization Application (MAA)
Global Regulatory Affairs leader for a combination of RA functions. Provides clear and specific regulatory input using skills(scientist, regulator and lawyer) to provide strategic planning decisions and implementation enabling successful drug approvals. Strong leader, expertise in DD, alignment with business goals, creative, proficient with complex frameworks and integration of abstract concepts in clinical and CMC areas o...
Tags for this Online Resume:
Regulatory Affairs, small molecules, CDER, CBER, FDA, EMEA, IND, NDA, CTA, IMPD, proteins, anti-infectives, cardiovascular, pain, oncology, CMC, compliance, communicator, monoclonal antibodies , Biologics, Food and Drug, Global, eCTD, health authorities, alliance management, combination products, Biologics Biosimilars , Director , pharmaceutical , Leadership, Problem solving , Innovation, experienced, IND NDA CTA MAA, business goals , biologics - pharmaceutical , biosimilars
Compliance Manager - 4 Years of Experience - Near 08827
Qualification Summary-Operations Manager Global Regulatory Affairs and Operations:
I possess a unique combination of well-developed marketing, sales, and training management skills with 4 plus years’ experience performing regulatory and operations management activities supervising all International Documentation and labeling statutory and regulatory requirements for the exportation of all Johnson & Johnson Consumer, Inc. c...
Tags for this Online Resume:
FDA, Operations Manager, Regulatory Affairs, Telecommute, Export, Global, New Jersey
Principal Scientist/Analytical Project leader
Seek position in R&D as a analytical development team leader handling multiple projects, coordinate project activities with various departments (quality assurance, Reg. CMC, Clinical Manufacturing Unit, Drug supply management, technical operations and outside contract laboratories. Direct analytical method development and oversee analytical development for the formulation development at contract labs
Tags for this Online Resume: Publications, Diagnostics, Pharmaceutical, Research, Research and Development, Support, Technical Support, Audit, Compliance, Medical