Regulatory Affairs Specialist

Philogen S.p.A.; Venezia; In loco; EUR 45.000 - 70.000; Tempo pieno

Descrizione del lavoro

A leading biotech company in Italy is looking for a Regulatory Affairs Specialist. This role involves managing submissions to regulatory agencies, developing strategies for product registrations, and collaborating with various teams. The ideal candidate will have at least 5 years of experience in regulatory affairs, a science-related university degree, and a strong understanding of FDA and EMA requirements. Competitive salary and contract relative to experience offered.

Servizi

Competitive salary based on experience

Competenze

• At least 5 years’ experience in regulatory affairs.
• Understanding of FDA and EMA regulatory requirements.
• Experience with electronic submission tools preferred.

Mansioni

• Lead activities for product submissions to regulatory agencies.
• Develop content and timelines for regulatory submissions.
• Coordinate preparation of regulatory submissions worldwide.
• Train clinical staff in regulatory policies.

Conoscenze

Excellent written and oral communication skills

Thorough understanding of ICH GCP

An excellent level of English

Experience in Regulatory Life Cycle Management

Formazione

University degree in science

Descrizione del lavoro

Philogen S.P.A., a biotech company listed on the Milan Stock Exchange and a leader in the development of innovative anti-tumor therapies, is expanding its clinical activities and will be opening a new office in Milan.

Philogen S.P.A. would like to hire a highly motivated and qualified Regulatory Affairs Specialist who will report to the Regulatory Affairs Manager and will provide support in formulating and implementing regulatory strategies for the development of Company Products in close collaboration with other functions in the Clinical Department.

In particular, the selected candidate will carry out the following tasks :

• Lead and manage activities concerned with the submission and approval of products and product transfers to government regulatory agencies including US and EU regulatory bodies :
• Develop content, timelines and contingencies for submissions in collaboration with internal and external contributors
• Ensure that submissions are of high quality, meet all regulatory requirements and comply with corporate goals and directives
• Reviewing draft registration files and submitting new and amended registration dossiers to obtain and maintain registration
• Gathering, evaluating, and organizing information necessary for regulatory agencies and other third parties;
• Coordinate and participate in the preparation of different types of regulatory submissions (e.G. dossier, variations, scientific advice submissions, INDs) to competent authorities worldwide for approved and developmental products
• Provide regulatory feedback to project teams and senior management
• Participate in contacting competent authorities for respective projects / products and interact with internal departments
• Performing the registration, update and posting of results of Philogen studies in mandatory clinical trials and publication databases;
• Management of procedures related to Marketing Authorisation Applications for EMA and FDA;
• Managing the update of the Trial Master File and archiving of the documentation regarding the Competent Authorities and Ethics Committees of all Philogen studies in collaboration with the CTA;
• Prepare and revise controlled documents including clinical Forms, Templates and Standard Operating Procedure (SOPs) referred to the Regulatory Affairs;
• Training clinical staff in regulatory policies or procedures;
• Keeping up-to-date with changes in regulatory legislation and guidelines and evaluating applicable laws and regulations to determine impact on department activities;
• Preferably experience of but definitely an awareness of the key electronic submission tools

Requirements :

University degree in science (preferred)

At least 5 years’ experience in regulatory affairs

Experience in Regulatory Life Cycle Management and eCTD is an advantage, although not required

A thorough understanding of ICH GCP and regulatory requirements worldwide (particularly FDA and EMA)

Excellent written and oral communication skills.

An excellent level of English, both written and spoken.

We offer :

A contract and salary proportional to the experience of the successful candidate

Job location :

Milano / Siena - Italy

We invite interested candidates to submit their applications expressly authorizing the processing of personal data in accordance with Legislative Decree 196 / 2003. Our recruitment adheres to the provisions of Legislative Decree 198 / 2006, and we welcome applications from candidates of any gender orientation or expression, sexual orientation, age, ethnicity, or religious belief.