Country Clinical Trial Manager / Local Trial Manager - Register your interest - FSP - Home Based

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.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Register your interest for future opening with us as a Local/Country Clinical Trial Manager in Italy.

In this role, you will be responsible for study and country level activities from start up through conduct and study close and have responsibility for study management aspects of assigned studies, including vendor and budget management.

This will be a fully remote home-based position.

Some specifics about this advertised role

• Regional/Country/Study level implementation of Start-up and Site Activation Plans

• Responsible for country/study level Recruitment Strategy

• Responsible to support the development of study level plans

• Communication with the local team and internal stakeholders and CRO partner as applicable and as listed above to ensure efficient and timely study delivery of the agreed plans

• Responsible for study and/or country vendor management and oversight including follow up and coordination of vendor deliverables

• The Country Study Operational Manager will be able to work independently and exercise their own judgement.

Who are Parexel

• Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.

• We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.

• You’ll be an influential member of the wider team.

What we are looking for in this role

• Minimum of 5 years of relevant end to end clinical trial management experience.

• Experience with customization or localisation of patient facing documents is essential

• Excellent leadership, communication, and organizational skills. Able to multi-task under limited direction and on own initiative.

• M.S/M.A/Ph.D or B.A/B.S/nursing degree is essential.

• Prior and demonstrable experience working at a senior level within Study start up preferred.