Associate Director, Clinical Affairs

buscojobs España; País Vasco; A distancia; EUR 70.000 - 100.000; Jornada completa

Descripción de la vacante

A leading company in the healthcare sector is seeking an Associate Director of Clinical Affairs to oversee clinical studies and manage a team of Clinical Study Leads. This role involves ensuring compliance with regulations while fostering talent and improving processes. The ideal candidate will have extensive experience in the in vitro diagnostic devices industry and strong leadership skills. Opportunities for professional growth and competitive benefits are offered in a dynamic international environment.

Servicios

Pension

Private Healthcare

Dental Care

Gym Membership

Flexible Working

Bonus Schemes

Formación

• At least 5 years of experience in in vitro diagnostic devices or clinical affairs.
• Strong knowledge of ISO13485, CLSI guidance, and ICH GCP.

Responsabilidades

• Manage delivery of diagnostic studies, ensuring excellence in planning.
• Lead and develop the Clinical Study Leads team.
• Continuously evaluate and improve clinical processes.

Conocimientos

Leadership

Project Management

Regulatory Compliance

Educación

University degree in a health-related field

Advanced degree preferred

Descripción del empleo

Associate Director, Clinical Affairs, remoto

Client : Qiagen

Location : remoto, Spain

Job Category : Other

EU work permit required : Yes

Job Reference : 283006469706612736032460

Job Views : 6

Posted : 31.03.2025

Expiry Date : 15.05.2025

Job Description :

Overview : At QIAGEN, our mission is to make improvements in life possible through advancements in science and healthcare. We are a global company with over 6000 employees across more than 35 locations. We value passionate professionals and are always seeking new talent to join our dynamic, international teams. If you want to make a real impact and advance your career, consider joining us.

Role : The Associate Director of Clinical Affairs will serve as an ambassador for the global clinical function. Responsibilities include managing a team of Clinical Study Leads, overseeing clinical studies for diagnostic assays and platforms, and collaborating with internal and external stakeholders to ensure high-quality, timely, and budget-compliant studies. Leadership duties involve team development, resource planning, and process improvements.

Key Responsibilities :

• Manage delivery of diagnostic studies within the business area, ensuring excellence in planning and budgeting.
• Lead and develop the Clinical Study Leads team, fostering talent and establishing a framework for growth.
• Continuously evaluate and improve clinical processes, ensuring compliance with evolving regulations and guidance.

Position Requirements :

• University degree or equivalent in a health-related field; advanced degree preferred.
• At least 5 years of experience in the in vitro diagnostic devices industry or related fields, including clinical affairs.
• Willingness to travel internationally (15-20%).
• Proven ability to manage multiple projects across various sites.
• Strong leadership skills with the ability to influence without authority and build rapport.
• Excellent knowledge of industry standards, including ISO13485, CLSI guidance, and ICH GCP.

What We Offer :

We provide opportunities for professional growth in an international environment, along with competitive benefits such as pension, private healthcare, dental care, gym membership, flexible working, bonus schemes, and more. We are committed to diversity and equal opportunity employment.

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