Global Study Manager (Oncology) France FSP

When our values align theres no limit to what we can achieve.

At Parexel we all share the same goal - to improve the worlds 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 were committed to making a difference.

About Parexel

Parexel is a leading global clinical development partner delivering insightsdriven clinical and consulting solutions to the life sciences industry. With 22000 employees worldwide we partner with biopharmaceutical companies and research sites to design and deliver patientfocused clinical trials that broaden access and make research a care option for anyone anywhere.

We work with focus agility and shared purpose moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking adapt quickly to change and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industryleading innovation With Heart.

About the Role

We are seeking experienced Global Study Managers (GSM) with strong oncology trials experience to join our team in a remote capacity in France. As a GSM you will be responsible for global study activities from start up through conduct and study close.

The Global Study Operations Manager has responsibility for study management aspects of assigned studies including vendor and budget management.

You will support clinical research activities that advance new treatments for patients and collaborate with global crossfunctional teams.

Youll join a fastpaced growthoriented environment focused on making a meaningful impact through the set-up execution and delivery of assigned trials and contribute to delivery of the sponsors pipeline through accurate planning and efficient execution of trials that bring speed and value to participating subjects and sites.

With diverse teams and continuous learning opportunities the Global Study Manager can explore career paths and expand skills across clinical research.

These will be fully remote home-based positions.

Key Responsibilities

• Global Study level implementation of Start-up and Site Activation Plans

• Responsible for global/regional study level Recruitment Strategy

• Responsible to support the development of global study level plans

• Communication with both global and local teams 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 vendor management and oversight including follow up and coordination of vendor deliverables

Candidate Profile

Youll thrive in this role if you bring:

• Extensive experience in clinical trial project management across international trials

• Global experience working in clinical research healthcare or a regulated environment

• The ability to collaborate across teams and communicate clearly

• A patientfocused mindset and strong attention to detail

• The ability to work independently and exercise your own judgement

Required Qualifications

• M.S/M.A/Ph.D or B.A/B.S/nursing degree is essential. (Masters is preferred)

• Minimum of 5 years relevant experience in clinical trial management

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

• Strong communication organization and problemsolving skills

• Fluency in English both written and spoken

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

If this job doesnt sound like the next step in your career but perhaps you know of someone whod be a perfect fit send them the link to apply!

We believe in flexibility growth and creating space for people to do their best work. Join us and be part of a team where your contributions help shape the future of clinical research.