At Ferrer we use business to fight for social justice.
We have long been a company that looks to do things differently; instead of maximizing shareholder returns, we reinvest much of our profit in initiatives that give back to society.
Back where it belongs.
We go beyond compliance and are guided by the highest standards of sustainability, ethics and integrity.
As such, since 2022, we are a B Corp. Founded in Barcelona in 1959, Ferrer offers transformative solutions for life-threatening diseases in more than one hundred countries.
In line with our purpose, we have an increasing focus on pulmonary vascular and interstitial lung diseases and rare neurological disorders.
Our 1,800-strong team is driven by a clear conviction:
our business is not an end in itself, but a way to change lives. We are Ferrer.
Ferrer for good.
Who we are
At Ferrer we are a group of people who believe in the power of purpose.
And our purpose is to make a positive impact in society and bring about change in an unjust world.
We are the 24/7 activists fighting for a sustainable planet, equal opportunities for all and a healthy workplace.
We reject greenwashing and empty promises - we are about action.
That is why in 2022 we became a B Corp company. Founded in Barcelona in 1959, our products are present in more than a hundred countries, and we have a team of over 1,800 people.
Professionals that we empower to become leaders of change and to build meaningful careers.
The Role
As Clinical Development Director, you will hold ultimate responsibility for the design, execution, and analysis of clinical trials (Phase I-IV), ensuring compliance with Ferrer's QMS, ICH/GCP EU & US standards, local regulations, and allocated budgets.
Leading a multidisciplinary team, you will oversee all clinical research functions, including project management, safety, monitoring, regulatory, and biometry.
This role is critical in driving clinical excellence and ensuring that Ferrer's clinical programs align with strategic goals, supporting the organization's mission to bring innovative solutions to market. The position will report to the Chief Scientific Officer, member of the Executive Committee of the Company.
What will the role do?
1. Lead the design, execution, and analysis of Phase I-IV clinical trials, ensuring compliance with Ferrer QMS, ICH/GCP, and local regulations.
2. Develop and oversee clinical development plans, including study protocols, safety oversight, and adherence to budgets and timelines.
3. Manage and optimize clinical operations, including resource allocation, vendor management, and monitoring activities.
4. Supervise and mentor a multidisciplinary clinical team, fostering professional growth and high performance.
5. Provide clinical support to corporate functions such as Regulatory, Pharmacovigilance, Legal, BD, and Quality.
6. Build and maintain relationships with investigators, research sites, and KOLs to enhance trial design and execution.
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