http://www.europetalent.com en-us info@europetalent.com http://www.europetalent.com/images1/gtsmall.JPG http://www.europetalent.com http://www.europetalent.com/home/Assistant-and-Interpretor-English-Ukranian-jobs-in-Kiev-Ukraine-292.html 1. Internet Data research (Processd Food, Animal Feed, Restaurants, Bakery, Logistics, Media, Homeshopping, Cinema, Retail, Travel, Resources) 2. Translation of Ukrainian data to English 3. Interpretation during field survey and meetings if necessary. 4. Other assistance for the Project Team. Working time : Mon~Fri 9am~6pm, Sat 9am~1pm Job duration : 17th March~End of April 2008 Ukrainian, English, Russian(option) Residing in Kiev Educational Background : BA (Business administration, Economy preferred) Work Experience : N/A Current Residence of the candidate : Kiev, Ukraine Language : Ukrainian, English (Russian Option) Skills : Web researching, MS Office (Word, Powerpoint, Excel) http://www.europetalent.com/home/Assistant-and-Interpretor-English-Ukranian-jobs-in-Kiev-Ukraine-292.html http://www.europetalent.com/home/Clinical-Research-Associate-jobs-in-Kiev-Ukraine-273.html Clinical Research Associate Responsible for monitoring all types of clinical trials; assures adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures. ESSENTIAL JOB FUCTIONS: COMMUNICATION •Maintains timely and effective communication among team members and site staff. REGULATORY DOCUMENTATION •Assures compliance with CFR, State regulations, ICH and GCP guidelines and INC Research and sponsor SOPs. •Maintains current regulatory documentation according to Essential Regulatory Document Guidelines (ERDG) and Trial Master File (TMF) Plan. •Participates in TMF and on-site audits as requested. MONITORING Assumes responsibility for site management and site staff performance including: •Monitors all types of clinical trials. •Participates in all types of site visits. •Assures Principal Investigator (PI) integrity. •Assures compliance with all protocol requirements. •Assures effective patient identification and recruitment plan is in place. •Assures timely reporting of AEs/ SAEs and Protocol Violations. •Regularly perform Investigational Product (IP) accountability. •Regularly review the status of contents of the site Regulatory Binder. DATA HANDLING •Performs source document verification (SDV) according to contractual requirements. •Assures timely completion and submission of CRFs according to Clinical Monitoring Plan (CMP) and / or Data Management Plan (DMP). •Assures timely and accurate completion of Data Clarification Forms (DCFs). •Performs clinical data listings reviews as needed. REPORTING AND TRACKING •Completes and submits visit trip reports according to SOP requirements. •Maintains awareness of key study performance indicators for own sites, e.g. patient enrollment, SAEs. •Updates study and patient status information and serves as (CTMS) resource for PM/LCRA. •Tracks Investigator payments/ milestones, if requested. •Documents and tracks the resolution of all outstanding site-specific protocol-related issues from visit to visit. ADMINISTRATIVE •Attends investigator’s meetings as requested. May assist with preparation. •Assists with the preparation of study start up materials and tools, as requested. •Attends clinical monitoring staff meetings, project team meetings, clinical committees, and clinical training sessions according to the project Communication, Monitoring and / or Training Plans. OTHER RESPONSIBILITIES •Performs other work related duties as assigned. •Demonstrated basic understanding of SOPs, WI, FDA and local regulations as well as ICH guidelines •Demonstrated basic understanding and knowledge of ongoing protocol and disease related terminology for study the individual is currently responsible •Basic knowledge of the Drug Development process •Ability to handle most aspects of site selection, site initiation, site monitoring and close out visit with minimal supervision •Extensive travel may be required (more than 50%). EDUCATION/SKILL/EXPERIENCE REQUIREMENTS: Requires a B.A. / B.S. in the science/health care field, nursing degree, or equivalent related experience. Preferably a minimum of one year clinical or research experience in CNS, Oncology, Pediatrics and/ or other related research experience. Ability to handle multiple tasks to meet deadlines in a dynamic environment is essential. Requires strong organizational, documentation and interpersonal skills as well as a willingness to work within a team-oriented environment. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint), email, and voicemail is required. Must have valid, current driver’s license and ability to secure corporate credit card. PHYSICAL REQUIREMENTS: Position requires: ordinary ambulatory skills and physical coordination sufficient to move about office locations; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of medium weights up to 50 pounds; arm, hand and finger dexterity, including ability to grasp and type for prolonged periods of time; visual acuity to use a keyboard, computer monitor, operate equipment, and read materials for prolonged periods of time; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time. The noise level in the work environment is low. Proven Knowledge of ICH/GCP Monitoring EDC CNS Oncology Infectious Diseases and Peadtrics all advantage http://www.europetalent.com/home/Clinical-Research-Associate-jobs-in-Kiev-Ukraine-273.html http://www.europetalent.com/home/Web-Developer-jobs-in-Kiev-Ukraine-127.html Our client, a technology start-up backed by a seasoned team of professionals, is seeking to recuirt a Web Developer. Working directly with on-site project manager as well as outsourced service providers like web designers, the Web Developer will be responsible for creating and modifying code that supports a number of business processes, including main web sites, business software, and database operations that support the Company operations. He/She will be coding mainly in PHP/MySQL environment but familiarity with VB/MS Access is also required. Responsibilities include: • Extensive PHP/MySQL coding for new projects or modifications in existing code. • Comprehensive assistance during product development life cycle including design, code development, system integration, testing, documentation and code maintenance. • Providing work estimates and deliver challenging, stable, and maintainable coding projects on schedule Compensation: Dependent on profile and experience. However, the successful candidate can expect an attractive performance-linked bonus, plus a basic salary. At least 2 years experience of focused web application development. • Very strong knowledge of PHP, MySQL, HTML and JavaScript. • Experience and familiarity with VB/MS Access. • Bachelor's degree in Computer Science (or equivalent degree/experience/certification) • Knowledge of Linux environment. • Working knowledge of SQL and database concepts. • Familiarity with Microsoft Tools. • Organization and detail-orientation, excellent oral and written communication skills. Personal attributes: • Ideal candidate would have a high level of intellectual ability, a structured and logical mind, great sense of curiosity, and incredible drive and energy. • He/she would have an insatiable appetite for technology and related issues (particularly in the online domain). • The candidate should ideally have blue-chip experience and training in a structured and professional environment. • Entrepreneurial experience / working with a start-up a plus. Ideal age range: 23-28 http://www.europetalent.com/home/Web-Developer-jobs-in-Kiev-Ukraine-127.html