Associate Director, Clinical Affairs

buscojobs España; Almería; A distancia; EUR 70.000 - 90.000; Jornada completa

Descripción de la vacante

A leading company in the diagnostics field is seeking an Associate Director of Clinical Affairs to manage clinical studies and lead a team. The role involves ensuring compliance with regulations and fostering talent within the team. Candidates should have a strong background in the industry and excellent leadership skills. The position offers opportunities for professional growth and competitive benefits.

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.
• Proven ability to manage multiple projects across various sites.

Responsabilidades

• Manage delivery of diagnostic studies, ensuring excellence in planning and budgeting.
• Lead and develop the Clinical Study Leads team.

Conocimientos

Leadership

Project Management

Compliance Knowledge

Educación

University degree in 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.