Jobs at Parexel
Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Site Monitor II - Poland - FSP
Job ID R0000032312 , PolandIf you want to be part of a leading CRO and transform scientific discoveries into new treatments, then Parexel FSP challenges you to live up to your potential by joining us at CRA, home-based, Poland.
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 success.
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 security and long-term prospects.
Our CRAs work from their home office base, supporting studies within their country or region. ‘Manageable sites, manageable protocols’ is our mantra. Expect exciting professional challenges in inspiring studies, but with time for your outside life.
The most significant aspect of this position is that
- You will be dedicated to a single client
- You will be responsible for all 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 as CRA in oncology (+3 years).
- Minimum 3 years’ experience in independent site monitoring of all 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, current GCP/ICH and country clinical research legislation and guidelines.
Our people and their passion are very important to us as they are the key to our success. That's why we provide you with an open and friendly working environment where we empower people and provide them with opportunities to develop their careers in the long term. In addition, you will have the opportunity to develop within your role and take on more responsibility or develop your skill set within other related Parexel FSP departments.
For an immediate interview, please contact marta.kuniewicz@parexel.com
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