Senior / Medical Director (Ophthalmology)

TFS HealthScience; Madrid; Presencial; EUR 100.000 - 140.000; Jornada completa

Descripción de la vacante

A leading Contract Research Organization is seeking a Senior / Medical Director in Ophthalmology to manage safety and medical matters, provide expert guidance on study designs, and support regulatory submissions. The role requires an MD with clinical experience, particularly in ophthalmology, and a strong understanding of GCP and regulatory standards. Join a team that values collaboration and innovation to make a difference in patients' lives.

Servicios

Competitive compensation package

Comprehensive benefits

Personal and professional growth opportunities

Formación

• At least 5 years’ experience in clinical practice.
• Experience serving on safety data review boards.
• Strong understanding of GCP and ICH guidelines.

Responsabilidades

• Provide advanced medical input on study design and trial protocols.
• Review safety data from a medical perspective.
• Contribute to regulatory submissions and safety-related documentation.

Conocimientos

Communication Skills

Regulatory Knowledge

Adaptability

Clinical Trial Expertise

Professional Credibility

Educación

Medical Doctor (MD)

Descripción del empleo

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.

Join Our Team as a Senior / Medical Director (Ophthalmology).

About this role

As part of our Ophthalmology team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals.

The Senior / Medical Director is a key member of the Project Delivery team, working independently to manage safety and medical matters in line with company policies, standard operating procedures (SOPs), and regulatory requirements. With deep medical expertise, this role serves as the primary authority on medical issues—providing clear, informed guidance and answering complex questions related to medical, legal, and regulatory concerns.

Key Responsibilities

Expert Guidance : Provide advanced medical input on study design, measurement strategies, and trial protocols, including safety sections and investigator brochures.

Comprehensive Safety Oversight : Review safety data such as adverse events, labs, vital signs, ECGs, and clinical trial reports from a medical perspective.

Regulatory & Risk Support : Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management Plans.

Medical Monitoring & Signal Detection : Serve as a medical monitor in trials, perform literature reviews, and contribute to signal detection and interpretation.

Regulatory Document Contributions : Offer expert medical insight into regulatory submissions and safety-related documentation.

Team & Client Engagement : Mentor junior medical staff, support SOP / tool development, and join Commercial Operations in client meetings and presentations.

Qualifications :

• Medical Qualifications : Medical Doctor (MD) with specialist medical training in Ophthalmologyand at least 5 years’ experience in clinical practice.
• Clinical Trial Expertise : Experience serving on safety data review boards or equivalent roles in clinical research.
• Regulatory Knowledge : Strong understanding of GCP, ICH guidelines, pharmacovigilance legislation, and internal SOPs.
• Adaptability : Comfortable working in fast-paced environments with shifting priorities and deadlines.
• Communication Skills : Excellent verbal and written communication, able to convey complex ideas clearly to diverse audiences.
• Professional Credibility : Trusted medical professional with a strong foundation in both clinical and research settings.

What We Offer

We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in the lives of patients

A Bit More About Us

Our journey began over 27 years ago in Sweden, in the city of Lund. As a full-service, global Contract Research Organization (CRO), we build solution-driven teams working towards a healthier future. Bringing together over 800 professionals, TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.

Our core values of Trust, Quality, Passion, Flexibility, and Sustainability are our guiding light serving as the framework for decision-making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments, resulting in high employee engagement and satisfaction. By aligning on these fundamental values, we cultivate a unified force, geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. Together we make a difference.