Country Study Operations Manager I - Spain - FSP

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Hiring Remotely in Spain
Remote
Pharmaceutical
The Role

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.

At Parexel FSP, people make a difference. We have a key mission: to prevent and treat disease by bringing important new medicines and therapies to patients in need. We achieve this important goal through the expertise, experience, innovation, and commitment of our employees around the world.

Our employees have the opportunity to do meaningful things around the world, while we support them locally in environments of challenge, collaboration, flexibility and industry-leading growth potential.
 

Parexel FSP is looking for a Country Study Operations Manager in Israel, 100% remote.
 

In this position, you will be responsible for studies and activities on a national level from inception, through execution to closure. You will be responsible for the management aspects of assigned studies, including vendor and budget management.
 

Expect exciting professional challenges, but with a healthy work-life balance. Your wellbeing is as important to us as our patients.

For each role, we look for professionals who have the determination and courage to always put the patient's wellbeing first. For us, this is a job with heart.
 

Some details of the role

- Implementation of commissioning and activation plans for sites at regional/national/research level.

- Responsibility for the recruitment strategy at country/study level.

- Responsibility for supporting the development of plans at survey level.

- Communicate with the local team and internal departments and the CRO partner, where applicable and as listed above, to ensure effective and timely delivery of agreed plans.

- Responsibility for the management and oversight of studies and/or country providers, including the monitoring and coordination of results delivered by providers.

- The Country Study Operational Manager I will be able to work independently and use their own judgement.
 

Experience required for this role:

- Required: BA/BS/BSc & 5+ years of relevant experience or MBA/MA/MSc & 3+ years of relevant experience.

- At least 4 years’ experience as Start Up Project Managers, Country Trials Managers, Site Activation Managers, and Clinical Trial Managers, Clinical Operations Leader.

- Experience in clinical trials management in Isreal is mandatory. 

- A scientific or technical degree is preferred with knowledge of clinical trial methodology.  

- Ability to manage, develop ideas and lead moderately complex projects and processes.

- Comprehensive knowledge of own discipline and good knowledge of other disciplines, applying skills to ensure study meets its goals.

- Supports an environment where innovation is standard taking appropriate risks to advance innovative processes

- Experience working at a senior level in a research start-up and site activation (at least in the last 2 years).

- Industry (pharma/biotech/CRO) experience.

- Oversight and leadership experience are needed.

- Experience from study start up through study conduct (end-to-end) is needed.

- Strong IT/technology skills and solid oral and written communication skills are needed to be successful with this client.

- Fluent in English, in addition to any local language requirement, if noted in the specific requisition

- Experience with country level oversight/management and leadership.

 

For more information, please contact [email protected]

 

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The Company
HQ: Durham, North Carolina
20,524 Employees

What We Do

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.

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