At PAREXEL, we believe that the power to work independently and intelligently should be yours every day. Your ability to understand our clients’ needs and achieve quality results is critical to our reputation as one of the best clinical research organizations (CROs) in the world.
As a Clinical Site Manager (CRA) within PAREXEL's Global Monitoring Operations Group, we support you with leading-edge technology, the highest caliber team members, and managers who know your strengths. If you're looking for flexibility and work-life balance, we're here to listen and help you move forward with your individual career path.
Check out the top traits we’re looking for and see if you have the right mix.
"One thing I enjoy about my job is when I see patients feel better with the new treatments; that is very gratifying. I always think about the pleasure our work can give patients and their loved ones."- Wagner – Associate Manager, Clinical Operations
We are one truly global team working together to propel each client´s journey ahead faster.
We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.
Work with industry leaders and subject matter experts.
The ability to innovate, ask “what if” and try new solutions without fear of failure.
Opportunity to work on a wide range of therapeutic areas and medical devices.
Competitive salaries and bonus structure based on individual metrics.
As a CSM, PAREXEL will offer you world class technology and training catered to your individual experience. You can anticipate less travel and a lower protocol load in comparison to industry peers. Your hard work will be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas, and an opportunity to advance your career in clinical research. If impact, flexibility, and career development appeal to you, please apply to learn more.
Your Key Accountabilities:
- Act as PAREXEL’s sole contact with assigned clinical sites
- Use your trial management expertise to oversee overall integrity of the study and problem-solving skills to promote positive working relationships with the site and staff
- Conduct qualification visits (QV), site initiation visits (SIV) and monitoring visits (MV) at assigned clinical sites; generate visit/contact report
- Review the performance of the trial at designated sites, ensuring the rights and well-being of human subjects are protected and are in accordance with protocol
- Evaluate the quality and integrity of the reported data, site efficacy, and drug accountability
- Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines Ensure compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s)
- Monitor completeness and quality of Regulatory Documentation and perform site document verification
- Substantial Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology
- Educated to degree level (biological science, pharmacy or other health related discipline)
- Demonstrates strong interpersonal, written, and verbal communication skills within a matrixed team
- Ability to work in a self-driven capacity, with a sense of urgency and limited need for oversight
- Client focused approach to work; flexible attitude with respect to work assignments and new learning
- Ability to manage multiple tasks, to evaluate a variety of unpredictable scenarios, and achieve project timelines; apply understanding of study protocol(s)
- Work ethically and honestly to promote the development of life changing treatments for patients
- Strong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS-Office products such as Excel and Word
Join the best minds in the industry and leverage your expertise to help advance treatments into the hands of those who need them most. This role is an excellent opportunity to enhance your skills and take the lead on client projects.
We look forward to speaking with you and determining how PAREXEL fits into your career journey!
EEO DisclaimerPAREXEL is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
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