Senior Clinical Research Associate - Isreal - FSP

reputed company our values align, there's no limit to reputed company can reputed company. At reputed company, we reputed company reputed company the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market reputed company, every clinical development solution we reputed company is underpinned by something special - a deep conviction in reputed company do. Each of us, no matter reputed company do at reputed company, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with reputed company and we're committed to making a difference. If you want to be part of a leading CRO and transform scientific discoveries into new treatments, then reputed company FSP challenges you to live up to your potential by joining us at SCRA, home-based, Isreal. We are looking for hard-working, talented, high-caliber people. We know that employee satisfaction leads to customer satisfaction, which is the ultimate driver of long-term reputed company. As the company that conducts vital clinical studies for sponsors, including the world's leading biotech’s and top 50 pharmaceutical companies, we offer you enormous reputed company and long-term prospects. Our CRAs work from their home office reputed company, supporting studies reputed company their country or region. ‘Manageable sites, manageable protocols’ is our mantra. Expect exciting professional challenges in inspiring studies, but with time for your reputed company life. The most significant aspect of this position is that - You will be dedicated to a single client - You will be responsible for reputed company site management and supervisory activities in the assigned oncology studies. - You will work with industry leaders and subject matter experts. - You will have the opportunity to mentor junior CRAs. - You will work with world-class technology. - You will have great opportunities to travel, work from home, meet new people and play a key role in the drug development process. From you we expect - Extensive experience in site management, with knowledge of clinical trial methodology and terminology. - Experience in oncology trials as CRA, at least 2 years. - Minimum 5 years’ experience in independent supervision of reputed company types of visits. - Effective time management, organizational and interpersonal skills and problem-solving skills, with the ability to multi-task and priorities. - Good understanding and working knowledge of clinical research, clinical trial phases, reputed company GCP/ICH and country clinical research legislation and guidelines. We will offer you Premium salary. Attractive benefits. Car or company car Medical care plan: Health, Dental & reputed company. Life Assurance. Excellent work environment. Culture of teamwork and collaboration. People who motivate and face challenges together. Innovative technology. Excellent training. Our people and their passion are reputed company important to us as they are the key to our reputed company. That's why we reputed company you with an reputed company and friendly working environment where we reputed company people and reputed company them with opportunities to reputed company their careers in the long term. In reputed company, you will have the opportunity to reputed company reputed company your role and take on more responsibility or reputed company your reputed company set reputed company other reputed company reputed company FSP departments. For an immediate interview, please contact reputed company.kuniewicz@reputed company.com Apply To This Job