Exec Director, Project Delivery - General Medicine

JR Spain; Barcelona; Presencial; EUR 60.000 - 100.000; Jornada completa

Descripción de la vacante

An established industry player is seeking an Executive Director for Project Delivery in Barcelona. This pivotal role involves overseeing project management teams, ensuring compliance with regulations, and mentoring staff. You will collaborate with various teams to deliver high-quality results that improve patients' lives. The company fosters a culture of authenticity and inclusivity, providing comprehensive benefits to support employee well-being. If you're passionate about making a difference in the biopharmaceutical sector and have a strong background in clinical research, this opportunity is perfect for you.

Formación

• Extensive clinical research experience in CRO, pharma, or biotech.
• Cross-functional project management experience in clinical trials.

Responsabilidades

• Oversees projects to ensure timely study launch and conduct.
• Collaborates with teams for operational input in proposals.

Conocimientos

Project Management

Clinical Research

Client Relationship Management

FDA Regulations Knowledge

Risk Assessment

Educación

BA/BS in Life Sciences

Nursing Degree

Herramientas

Microsoft Office Suite

Descripción del empleo

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Exec Director, Project Delivery - General Medicine, Barcelona

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Client:

Location:

Barcelona, Spain

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

818036964168459878432460

Job Views:

2

Posted:

31.03.2025

Expiry Date:

15.05.2025

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Job Description:

Description

Executive Director, Project Delivery

Come discover what our 25,000+ employees already know: work here matters everywhere. We’re a growing biopharmaceutical industry leader, offering endless opportunities to work with global experts and build your dream career. As part of Syneos Health, you’ll help us deliver results that matter—improving patients’ lives worldwide. To us, a patient isn’t just a number, they’re family, friends, and neighbors.

Why Syneos Health

#SyneosHealthLife means we’re committed to our Total Self culture—where everyone can be authentic. Our culture unites us globally, and every individual’s contribution makes a difference. We value your dedication to care, and we support your well-being through comprehensive health, mental, and financial benefits. We’re continuously building the company we all want to work for, embracing diversity of thoughts, backgrounds, and perspectives to foster a sense of belonging.

Equal Opportunities Plan

• Achieves equality of opportunity in employment practices
• Ensures our workforce is representative of all genders and respects every employee, providing equal working conditions

Job Responsibilities:

• Provides oversight for all assigned projects to ensure timely study launch, conduct, and closeout, according to contractual agreements and quality standards, SOPs, GCPs, ICH guidelines, and regulations.
• Forecasts, prioritizes, and directs staff to meet sponsor deliverables with quality and within scope and expectations.
• Collaborates with Therapeutic Strategy and Innovation teams for operational input in proposals and pricing, including operational strategies.
• Prepares and facilitates bid defense meetings with the team and Business Development.
• Oversees project management teams in managing financial aspects such as contracts, change orders, forecasting, and invoicing.
• Mentors project delivery staff in leadership, customer management, project management, compliance, and specific tasks.
• Troubleshoots project difficulties, manages escalations, and facilitates communication and team building.
• Develops knowledge of therapeutic trends, competitive landscape, and drug development.
• Supports risk assessment and mitigation to ensure patient safety, data integrity, and quality delivery.
• Participates in project risk review processes and shares lessons learned and best practices.
• Supports change management initiatives and maintains senior relationships with clients through regular meetings and forums.
• May have direct reports.

Qualifications:

• BA/BS in life sciences, nursing, or related field, with extensive clinical research experience in CRO, pharma, or biotech industries.
• Cross-functional project management experience within clinical trials is required.
• Experience in pharma/CRO, including client relationship management.
• Thorough knowledge of FDA regulations, drug development, and clinical monitoring.
• Proficiency with ICH/GCP guidelines and Microsoft Office Suite.
• Ability to manage multiple tasks in a dynamic, matrix environment, ensuring timely, quality project delivery.