Regulatory Affairs Lead- FSP

Thermo Fisher Scientific; Lugo; Presencial; EUR 50.000 - 90.000; Jornada completa

Descripción de la vacante

Thermo Fisher Scientific is seeking a Regulatory Affairs Lead in Lugo, Spain, to manage clinical trials and provide strategic regulatory direction. The ideal candidate will have extensive experience in regulatory affairs, especially within EU regulations. You will work closely with clients to ensure compliance and lead a team of professionals, fostering a collaborative environment to achieve successful project outcomes.

Servicios

Flexible working culture

Extensive benefits package

Collaborative environment

Formación

• 8+ years of relevant experience in regulatory affairs.
• Strong understanding of global and EU regulatory requirements.
• Excellent written and verbal English communication skills.

Responsabilidades

• Lead regulatory strategy for clinical trials across multiple countries.
• Provide regulatory expertise and guidance throughout product development.
• Ensure compliance with local and international regulatory standards.

Conocimientos

Attention to detail

Interpersonal skills

Analytical skills

Problem-solving skills

Educación

Bachelor's degree

Herramientas

Microsoft Word

Microsoft Excel

Microsoft Power Point

Descripción del empleo

Join to apply for the Regulatory Affairs Lead- FSP role at Thermo Fisher Scientific

Join to apply for the Regulatory Affairs Lead- FSP role at Thermo Fisher Scientific

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Our Global Regulatory Affairs team is expanding! We are looking for a Regulatory Affairs Lead position to work for one of our key clients.

This a client dedicated role for a Regulatory Affairs Lead role : clinical expert role to support clinical trial new indications, including the early indications, early development and late development, and that can support later development. Global experience is a plus, EU CTR experience will be important.

The Reg Affairs Lead will act as the lead over several countries / projects in providing innovative solutions including regulatory expertise and client interface to provide strategic regulatory intelligence, and guidance supporting product development from preclinical through registration and product optimization. They will provide strategic, expedient and efficient preparation of client deliverables that meet current local, regional and ICH regulatory and technical requirements. They will also act as liaison with internal and external clients in the provision and marketing of these services.

Essential Functions :

• Provides senior review of regulatory documents and submissions created within or outside of the company in order to ensure high quality standards that meet or exceed client expectations, local and regional requirements.
• Acts as subject matter expert in providing regulatory strategy advice to internal and external clients on projects of moderate complexity. Provides internal clients with up-to-date legislation and guidance as it becomes available.
• Participates in project management activities to support the provision of regulatory services, and acts as liaison with internal and external clients in the provision of marketing these services.
• Provides matrix / project leadership, training and guidance to junior team members to support understanding of regulations, impact on study, assessment of risk, etc., and to achieve a specific goal and / or project deliverables.
• May provide input on performance reviews to management.
• Ensures adherence to project budgets, time schedules, and scope of work.
• Ensures compliance with relevant organizational and regulatory SOPs and WPDs.
• Contributes to business development activities, including project budgeting / forecasting.

Qualifications :

Education and Experience :

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years).
• In some cases an equivalency, consisting of a combination of appropriate education, training and / or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities :

• Excellent English language (written and oral) communication skills as well as local language where applicable
• Great attention to detail and quality as well as excellent editorial / proofreading skills
• Strong interpersonal skills to work effectively in a team environment and act as a liaison with other departments
• Strong computer skills including the use of Microsoft Word, Excel, Power Point; capable of learning new technologies
• Solid organizational, time management, and planning skills to create and follow timelines, conduct long-range planning, adapt to changing priorities and handle multiple projects
• Capable of working independently and exercising independent judgment to assess sponsor regulatory needs and work with project team members to producing compliant deliverables
• Strong understanding of global / regional / national country requirements / regulatory affairs procedures for clinical trial authorization, licensing, lifecycle management; expert knowledge of ICH and other global regulatory guidelines; good understanding of a regulatory speciality areas, clinical, in particular Clinical Trial Applications (CTA) including proven experience in submissions according to EU Clinical Trial Regulation.
• Experience in Global CTAs would be an advantage.
• Strong understanding of medical terminology, statistical concepts, and guidelines
• Excellent analytical, investigative and problem-solving skills
• Solid understanding of budgeting and forecasting
• Able to preform Line Managment responsibilities

What we offer :

As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD Clinical Research Services truly value a work-life balance. We’ve grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organisation but with a local feel.

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Apply today! Fisher Scientific is an EEO / Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Seniority level

Seniority level

Not Applicable

Employment type

Employment type

Full-time

Job function

Job function

Quality Assurance, Product Management, and Engineering

Pharmaceutical Manufacturing and Biotechnology Research

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