Clinical Trial Manager - Part Time - FSP - (,, United Kingdom)
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Clinical Trial Managers at Parexel FSP play a pivotal role in supporting, coordinating, and delivering our clients’ regional and global clinical trials. This includes full involvement in study start-up, maintenance, and close-out, as well as vendor management and CRA oversight.
Our CTM's each work with one sponsor exclusively, in a truly collaborative partnership. We offer exceptional financial rewards, training, and development. Expect exciting professional challenges, but with a healthy work/life balance.
Some specifics about this advertised role
* 100% home based
* Part Time: 0.7 FTE
* Work on Phase I regional or global trials.
* Oncology specific clinical trials
* Biotech, sponsor dedicated opportunity
* Lead member of a strong study management team (trial dependent)
* Start-up planning and vendor management responsibilities
* Play a key role in handling high profile and sensitive operations, taking a study to the next level.
Due to the nature of our projects and sponsors, we hire more experienced Study Managers, who have already spent several years in the role, with global study experience.
What we look for in Clinical Trial Managers
Precise requirements for each CTM's role vary from sponsor to sponsor, but generally we look for people with at least 5 years’ direct experience as a global study manager.
* Past exposure to trial start-up, maintenance, and close activities.
* Experience of overseeing CRAs, vendors and deliverables globally.
* The ability to work effectively with a wide range of clinical, technical, biometric, and regulatory stakeholders, as well as with sponsors.
* In depth experience working within international Oncology trials.
* Demonstrated experience in managing per subject costs, vendor and ancillary, and monitoring costs projections and spend.
* Experience of following milestones for the region with the local team.
* Experience in Phase I trial and CRO management.
* Experience of coordinating the EC submission in participating countries.
Just finally, we value work-life balance. We aim to keep regular hours and maintain our lives outside the office. We’ll value your welfare just as highly as that of our patients. And our managers will listen to, and act on, any concerns.
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