Associate Director, Clinical Risk Management

Johnson; Madrid; Presencial; EUR 90.000 - 130.000; Jornada completa

Descripción de la vacante

Johnson & Johnson in Madrid is seeking an Associate Director, Cross Therapeutic Area Clinical Risk Management to join our R&D Quality CRM team. You will lead risk identification, assessment, and mitigation for clinical trials, ensuring data integrity, patient safety, and regulatory compliance across multiple jurisdictions.

The role requires strong collaboration with trial teams and program leadership, delivering risk-based oversight, inspection readiness, and continuous improvement of risk

Formación

• Experience leading clinical risk management for trials or programs.
• Experience coordinating across trial teams and risk owners.
• Strong understanding of regulatory expectations and quality systems.

Responsabilidades

• Identify and assess key risks in protocols and study setup; advise on mitigations.
• Lead regular risk reviews with Risk Owners to track mitigation progress.

Conocimientos

Clinical Risk Management

Quality Assurance

Regulatory Compliance

Cross-functional Collaboration

Risk Assessment

Descripción del empleo

Associate Director, Clinical Risk Management

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Quality

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Quality

Job Sub Function:

Clinical Quality

Job Category:

Professional

All Job Posting Locations:

Beerse, Antwerp, Belgium, Madrid, Spain

Job Description:

Johnson & Johnson is currently seeking an Associate Director, Cross Therapeutic Area Clinical Risk Management to join our R&D Quality CRM team located at a J&J office in Spring House, PA; Horsham, PA; Titusville, NJ; Raritan, NJ; Beerse, Belgium; Basel, Switzerland; High Wycombe, UK; Madrid, Spain.

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):

United States - Requisition Number: R-083139

Switzerland - Requisition Number: R-085157

United Kingdom - Requisition Number: R-085163

Belgium/Madrid - Requisition Number: R-085167

Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

Job description to follow:

The Associate Director, Cross TA Clinical Risk Management, works with the trial teams and/or Program teams to coordinate the identification, assessment, and mitigation of quality risks that could impact ontrial data integrity, patient safety,well –being, or rights.Throughout the duration of the trial/program, this Associate Director executes data-driven, risk-based trial oversight activities to deliver quality in the execution of clinical trials (and/or programs), compliance with regulatory requirements and internal procedures, and tomaintaina continued state of inspection readiness.

Key responsibilities:

• Actively and independently participates in all study activities, contributing to the identification and assessment of key risks in the clinical protocol/set-up and advising clinical team members on effective mitigation strategies for complex clinical trials, compounds and programs.
• Leads regular review of risk areas in collaboration with Risk Owners, to evaluate progress of risk mitigations and risk reduction, and to identify potential new risks or additional mitigation needs (