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Online Resumes with "Adverse Events"
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.
Challenge, teamwork, espirit de corps, interchangeability, versatility, and best of breed service / products are elements that would pique anyone's interest, including mine!
Multitasking people person, good communicator, hard working, eager to learn new things
Have the experience and the knowledge of the clinical trial processes (start-up through close-out), including FDA regulations
Social/Clinical Trials Research Assistant/Coordinator/Clinical Support Specialist
Tags for this Online Resume: ICH Guidelines, IND Application, Guidance on HIPAA Privacy in Research, Protocol Amendment, Quality Assurance (QA), Serious Adverse Events (SAE) or Serious Adverse Drug Reaction (serious ADR), Source Document, Randomization
I am looking for a rewarding full-time position where my RN degrees and Pharmaceutical/Medical Device experience can merge together towards a management position.
Profile: Certified Clinical Research Associate professional with extensive recent focus in CVS research and clinical trials. Combine resourcefulness and problem solving skills with clinical knowledge to consistently deliver improved research and production results. Team player dedicated to quality, continuous improvement and bottom-line objectives. QUALIFICATION HIGHLIGHTS • Knowledgeable in all areas of research including...
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.
Seeking for a challenging career in a progressive organization offering the opportunity for contributing my skills services to the organization and personal growth and to work sincerely with maximum effort using best talents and with a challenge to achieve required goals and targets, abiding to the decisions of seniors and to earn a good reputation what ever required.
Tags for this Online Resume: Develop, maintain and manage appropriate study documentation, Developing, writing and presenting the clinical trial protocols, Initiate, maintain and reconcile Trial Master File., Monitoring the trial throughout its duration which will involve visiting the Study centers on a regular basis to check the patient data in the case report forms (CRFs) and to sort out any problems which may arise., Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other Data collection tools by careful source document review Monitor data for missing of implausible data., Complete Serious Adverse Event (SAE) reporting, process production of Reports, narratives and follow up of SAEs and managing the clinical data intermilitently as per 21CFR USFDA guidelines, Monitor study sites independently according to protocol monitoring guidelines, S.O.P.s, GCP and ICH Guidelines., Independently perform CRF review; query generation and resolution against established data review guidelines on client data management systems as assigned Perform other duties as assigned by management., , maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned
Highly Experienced, Deidicated, Ethical, Compassionate Medical Professional with Diversified Background.
I am looking for a position working with clients with varying levels of medical attention. I am looking to Supervise and train medical staff to develop a team of consistant, high quality, cohesive team members who enjoy what they do. I am a skilled professional medical assistant, office supervisor with several years experience training, managing and hiring medical team members with a focus on developing a staff with indiv...
Tags for this Online Resume: Supervisor, Phlebotomist, Customer Service, Medical Assistant, Team Development, File Manager, Adverse Event Reporting, Office Inventory Control, Team Facilitator, Office Manager, Medical Office Manager, Patient Focused, Microsoft Office Proficient, Highly Able to learn new systems
I would like to find a position where I can use my strong scientific backgound and my healthcare industry experience either in a pharmacovigilance area or a regulatory affairs type position dealing with submission of various research documents to the FDA.
Tags for this Online Resume: Regulatory affairs, adverse event, Bilingual, Regulatory, product complaint, Spanish, medical terminology, market research, documentation, pharmaceutical, devices, women's health, osteoporosis