Study Operations Manager I - Spain - FSP
Spain, Remote 求人ID R0000029854 Category Clinical TrialsAbout this Role
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 Study Operations Manager in Spain for 4 - 6 months contract, 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:
- Minimum of 2 - 3 years relevant experience in clinical trial management.
- Excellent leadership, communication, and organizational skills. --
- Ability to multi-task under limited direction and on own initiative.
- Master's/Bachelor’s degree/Doctorate or Bachelor's degree/Nursing is essential.
- Experience working at a senior level in a research start-up and site activation.
For more information, please contact marta.kuniewicz@parexel.com
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