Principal Reg Affairs Specialist (Remote) Lazio

Principal Reg Affairs Specialist (Remote)
Roma
Lazio, Lazio

Principal Reg Affairs Specialist (Remote)

Thermo Fisher Scientific

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 are currently seeking a Principal Regulatory Affairs Specialist to join our global Regulatory Affairs department Regulatory Science team. This is a fantastic opportunity to further develop your regulatory career and expertise in a global clinical trial setting.

On this role you will be a pivotal team member with regulatory affairs responsibilities, leading discussions, and coordinating regulatory strategies globally on assigned (Phase 1 to 4) clinical trials, studies, and projects.

The following skills are required to be successful in this position:

Preparation and assembly of global regulatory submissions

Interacting with sponsors

Review and assess clinical trial regulatory documents

Review and assess scientific literature

Manage project teams and preparation

Participate in launch meetings, review meetings, and project team meetings

Experience with bid defense meetings

Education and Experience:

Bachelor's degree or advanced degree preferred, or equivalent and relevant formal academic/vocational qualification. Previous experience that provides the knowledge, skills, and abilities to perform the job around 8+ years.

Knowledge, Skills and Abilities:

Excellent command of the English language (written and oral) as well as local language where applicable

Excellent attention to detail and quality as well as excellent editorial/proofreading skills

Exceptional interpersonal skills to work effectively in a team environment and act as a liaison with other departments

Advanced computer skills including the use of Microsoft Word, Excel, PowerPoint; capable of learning new technologies

Strong 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 produce compliant deliverables

Excellent understanding of global/regional/national country requirements/regulatory affairs procedures for clinical trial authorization; expert knowledge of ICH and other global regulatory guidelines

Excellent analytical, investigative, and problem-solving skills

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. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Apply today!

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.

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