FAQs
What is the primary responsibility of the Associate Director, Trial Clinical Delivery Lead?
The primary responsibility is to ensure the success of Phase I-IIIb Clinical Development studies by overseeing study, country, and site-level activities, serving as the primary contact for site management and operational issues.
What qualifications are required for this position?
A graduate degree in Medical or Life Sciences or equivalent is required, along with over 10 years of clinical research experience within CRO, pharma, or biotech.
Is experience in specific therapeutic areas necessary for this role?
Yes, desired experience in Oncology, Neurology, or Immunology is preferred.
What skills are essential for the Associate Director position?
Essential skills include adaptability, critical thinking, communication, analysis, risk assessment, and problem-solving abilities.
Will travel be required for this role?
Yes, travel may be required, with an expectation of up to 20%.
In what regions can this position be based?
This position can be based in any city in Spain.
What strategies will the Associate Director implement to enhance study performance?
They will implement operational excellence strategies, foster data-driven planning and accountability, collaborate on patient-directed recruitment strategies, and lead process improvement initiatives.
What qualities do you look for in an ideal candidate?
An ideal candidate should possess strong communication skills, the ability to work independently, effective task management capabilities, and expertise in clinical development principles and regulatory environments.
What is the company's stance on diversity and inclusion?
The company celebrates all dimensions of diversity and is committed to creating access and opportunities for all, fostering a culture of inclusion and belonging.
How can I apply for this position?
You can apply for the position by submitting your application through the company's career portal or designated application process.