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Online Resumes with "document review"
Fast paced work environment full of challenge and reward. A place where talents, training and experience are appreciated and compensated. An environment where the term phrase "team player" is not just a cliche. An employer who understands that "value and quality" of an applicant is not just found on the parched paper of a resume presentation but sometimes is also found in those applicants who the least of them. Would really...
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
Title Examiner on Legal Documents pertaining to property for Insurance purposes for more than 12 years.
To learn what needs to be done, then learn as much as can to move up as knowledgeable as possible, without stepping on anyones toes.
To obtain career stability with a mid level solid company proven good ethics and values as their strongest asset.
Managed R&D lab and developed team of 30 chemists. Duties included documentation and internal audits, report reviews, SOP and method validation reviews and employee recruitment and training. • Ensured on-time release of product to meet clinical trial timelines for Oxycodone and Acetaminophen Capsules, USP and Oxycodone tablets by meeting with development team on a weekly basis. • Ensured other approved products passed F...
To establish myself in a positive career where excellent communication skills, a high degree of professionalism, and a desire for mutual as well as individual growth is expected and rewarded.
Ideal Companies: Companies focused on providing a meaningful service to people
Looking for a company where I can utilize my experience working for the owner, architect and contractor to assist the company in constructing first class facilities and allows me to continue my professional growth through practical and educational training.
Ideal Companies: Engineering News Record Top 150 Construction/Project Management Companies
I'm notlooking for a particular style of company. I would prefer to work with a company that can put the skills I have to work for them. Accounting, Adminitstrative, and Customer Service.
my goal is to work as a quality control
Seeking a paralegal, legal assistant or document review position deploying over 15 years’ legal team experience, trial preparation, organizing, analysis, legal research, writing, training, administrative skills, and helping clients succeed.
Tags for this Online Resume: CaseMap
Continual learning of various positions in clerical and lifetime learner.
Ideal Companies: I like working for small and large companies.
Quality Bio-Pharmaceutical professional with ISO/GMP/TQM experience and strong data management in inventory control & distribution. Ability to design, develop and improve process systems. Bi-lingual in Spanish and English. Additional skills and knowledge include: Package & Labeling Design; Documentation Editing; Contract Facility Audits; Statistical Analysis; Return Destruction Processing; Charting Trending; Contract Vende...
Ideal Companies: Open to all Medical device and bio pharmaceutical companies