COVANCE TURKEY - CRAs (all levels) needed! Up to 5000 USD bonus for we
Nr ref.: /JOBS.pl
Covance is probably enhancing your quality of life without you even knowing it. We play an important role in bringing new therapies to market by helping to turn raw compounds into safe, effective, and approved drugs that help people live longer, more productive lives. Our mission - bringing medical miracles to market sooner - impacts the lives of millions of people all over the world. Our current growth of Clinical Development Services (CDS) in Eastern European countries brings new opportunities not only for clinical roles, but also another business functions.
CoSource, our insourcing division provides you with the opportunity to work directly for our clients. For these roles you will either work out of our client offices or field based - and see clinical trials from the clients' perspective. We work in partnership with global and smaller pharmaceutical companies and can support you in your career development.
As CRA you will be responsible for all aspects of study in Turkey: coordinating monitors, assistants, study budget and vendors:
Serve as lead monitor for a protocol or project and may assist in establishing monitoring plans as assigned; Review progress of projects and initiate appropriate actions to achieve target objectives; Organize and make presentations at Investigator Meetings; Interact with internal work groups to evaluate needs, resources and timelines; Act in the project role of as Local Project Coordinator or Lead CRA; Site administration responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP; Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor; Negotiate study budgets with potential investigators and assist the Covance legal department with statements of agreements as assigned; Assist with training, mentoring, and development of new employees, e.g. co-monitoring.
Required skills, experience:
Excellent site monitoring and management skills; Minimum 2-3 years (CRA) and 5 years (SrCRA) of relevant clinical research experience in pharmaceutical or CRO industries; Experience in leading projects - as a Lead CRA or local Project Manager; Experience in cardiology and neurology therapeutic areas; Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements; Ability to train and supervise junior staff; Ability to work under minimal supervision.
University Degree (life science) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology); Fluency in Turkish and English language.
In return, we offer you the opportunity to develop your career with an international organization; to pursue further training and to take advantage of our flexible conditions and attractive remuneration package.
We offer a special bonus up to 5000 USD for well experienced CRAs!
For more information and to apply online visit , quoting reference number: 45560BR.
Covance is committed to diversity in the workplace and is an equal opportunity employer. Your confidentiality and privacy are important to us.
Key words: Clinical trial, Clinical research, research monitoring, on-site monitoring, remote monitoring, clinical operations, GCP, ICH, SOP, CRO, Clinical Research Associate I, II, Senior CRA, Clinical Research Associate 1, 2, Clinical Monitoring Associate, Clinical Trial Monitor, Clinical Research Monitor, CRA I,II, Senior, CRA 2, CMA, CTA, in-house monitor, in-house CRA, home based, office based, Turkey, Istanbul