Safety Scientist II/ III, EMEA

ThermoFisher Scientific; España; A distancia; EUR 52.000 - 78.000; Jornada completa

Descripción de la vacante

Thermo Fisher Scientific is seeking a Pharmacovigilance Scientist to oversee signal detection and product safety activities, coordinating across trials and post-marketing programs. You will mentor colleagues, help develop processes and tools, and lead small projects under senior supervision.

The role requires a Bachelor's degree and 5+ years in pharmacovigilance, with strong data interpretation, medical writing, and English communication. Office-based in Spain with Monday–Friday schedule.

Formación

• Bachelor's degree required; 5+ years in pharmacovigilance preferred.
• Expertise in pharmacovigilance across major markets.
• Strong data interpretation and medical-writing skills.
• Solid project management abilities with multitasking across projects.

Responsabilidades

• Contribute to signal detection and product safety tasks across product life cycles.
• Lead small FSP projects under supervision.
• Mentor junior colleagues and develop processes/tools.
• Coordinate client communications, audits, and reviews.
• Ensure compliance with regulations and company policies.
• Collaborate across teams and systems to deliver safety deliverables.

Educación

Bachelor's degree

5+ years pharmacovigilance experience

Herramientas

Microsoft Office

Descripción del empleo

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

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 detailed, goal-oriented team members manage the safety profile of new drugs in clinical trials, oversee case-processing activities through all phases of development and perform regulatory reporting and medical monitoring tasks.

We hire the best, develop ourselves and each other, and recognise the power of being one team. We offer continued career advancement opportunities, award-winning training and benefits focused on the health and wellbeing of our employees.

A Day in the Life:

Responsible for the planning, coordination and delivery of signal detection and product safety scientist activities, with a focus on tasks which are low to high in complexity or which concern low to high complexity products. Additionally supports mentoring of more junior colleagues, development of processes/tools/systems, and may serve as lead on smaller FSP-type projects.

Essential Functions:

• Serves as a creator/contributor for signal detection and product safety scientist tasks which are low to high in complexity, or which concern low to high complexity products.

• Serves as a creator/contributor for signal detection and product safety scientist tasks which are ultra-high in complexity, or which concern ultra-high complexity products, under supervision by a more experienced team member.

• Conducts quality review for signal detection and product safety scientist tasks which are low to high in complexity, or which concern low to high complexity products.

• Advises clients on safety related issues under supervision by a more experienced team member.

• Leads small FSP projects.

• Supports training and mentoring of junior colleagues.

• Contributes to development of processes, tools and systems.

• Participates in bid defence and proposal development activities.

• Works within multiple company and client systems. Interacts with project team members and clients.

• Ensures that tasks are conducted in accordance with company policies and procedures, contractual agreements, and applicable regulations.

• Participates in departmental initiatives; Serves as a subject matter expert in designated area.

• Responsible for routine project implementation and coordination for assigned projects, including leading kick-off meetings, coordination of communications and data requests, participation in client meetings, audits and inspections, and review of metrics and budgets.

• Works on complex issues where analysis of situations or data requires an in-depth evaluation of variable factors.

• Having wide-ranging experience, uses professional concepts and company objectives to resolve complex issues in creative and effective ways.

• Determines methods and procedures on new assignments and may coordinate activities of other personnel (i.e., Team Lead). Exercises' judgment in selecting methods, techniques and evaluation criteria for obtaining results.

• Frequent contacts with internal personnel and outside customer representatives.

Keys to Success:

Education and Experience:

Bachelor's degree

Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).

Knowledge, Skills and Abilities:

• Expertise in pharmacovigilance requirements relating to marketed products and clinical trials across all major markets

• Excellent attention to detail, data interpretation and medical-scientific writing skills

• Advanced critical thinking and problem-solving skills with ability to evaluate and elevate appropriately Solid project management skills with the ability to manage multiple projects simultaneously and ability to redress issues proactively with limited management intervention

• Ability to motivate, mentor and provide guidance to less experienced staff, routinely exhibiting robust and proactive scientific expertise

• Proficient at complex project administration including budget activities and forecasting

• Excellent oral and written English language communication skills, including paraphrasing skills

• Advanced computer skills with the ability to work within multiple systems; advanced skills in Microsoft Office products (including Outlook, Word, and Excel)

• Ability to maintain a positive and professional demeanor in challenging circumstances and to proactively plan for likely scenarios using personal experience

• Ability to work effectively within a team to attain a shared goal

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.

Thermo 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.

Thermo 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.