New CRA II & SCRA jobs in Covance Madrid : sponsor dedicated, ph I-III oncology clinical trials. Generous Welcome Bonus if you join us now! Top 5 pharmaceutical client Following the 2017 acquisition of Chiltern, Covance Functional Service Provider (FSPx or sponsor dedicated) model, boasts one of the world's largest dedicated FSP groups in the contract research organization (CRO) space with 4,600+ staff in 60+ countries WHERE WILL YOUR CURIOSITY TAKE YOU?
Covance Spain are living an unprecedented growth and we are in the position of offering a wide variety of Clinical Research Associate II (CRA II) and Senior Clinical Research (SCRA) job opportunities If your ambition is to work sponsor dedicated , we have the right job for you.
Experience the stability of working with just one sponsor company and being part of two families who are both interested in your development and welfare.
WHAT MAKE THESE JOBS SPECIAL? Generous Welcome Bonus if you start the recruitment process now! Career progression will be exceptional : unlike other CROs, there are not fixed boundaries between our teams : we offer flexibility with great opportunity togrowinto a variety of areas such as Project Management, Clinical Team Leadership, Line Management and cross border roles.
Unlike some CRA roles you will not be pushed to satisfy unrealistic u2018monthly visit' targets With us, you will become anexpert in oncologytrials, learning how to overcome the complexities and challenges of oncology drug development and how to prevent the pitfalls that derail many onco trials.
Competitive salary and benefits package, including lunch vouchers and flexi time We know how to do it!As a clinical service provider, Covance has been engaged in global FSP relationships with biopharmaceutical clients for 30 years in 57 countries : You will be joining a large team with a well organised structure and robust processes in place.
Our employees make a difference in the lives of millions of people u2026 and you will too. Join us and see why LabCorp / Covance have been named for the second consecutive year to FORTUNE u00B4s 2019 List of World u00B4s Most Admired Companies u00B4 and more than 90% of the top 20 global pharmaceutical companies are repeat customers.
computer literacy) Good organizational and time management skills, able to work highly independently OTHER INFORMATION These jobs are full time & permanent positions to be employed through Covance.
For more information please contact Carlos Villanueva on +34 648 853 615 or mailcarlos.villanueva covance.com Education / Qualifications : University or college degree, or certification in a related allied health profession from anappropriately accredited institution (e.
g., nursing licensure) Thorough knowledge of regulatory requirements Thorough understanding of the drug development process Fluent in Spanish & English, both written and verbal Experience : Extensive clinical monitoring experience in Spain is needed, minimum 2 years monitoring studies in Oncology / Infectious diseases / HIV with proven track record of pre-study, initiation, routine monitoring and closeout visits.
Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs Ability to resolve project-related problems and prioritize workload for self and team Advanced site monitoring &study site management skills Ability to work with minimal supervision Good planning and organization skills Good computer skills with good working knowledge of a range of computer packages Locations : Madrid, Spain