Senior Regulatory Affairs Consultant - Life Sciences

NNIT

Follonica

In loco

EUR 90.000 - 130.000

Tempo pieno

11 giorni fa

Ricevi più risposte dai datori di lavoro

Invia un CV specifico per questa offerta in pochi minuti.

Descrizione del lavoro

NNIT is seeking a Senior Consultant in Regulatory Affairs to join our European regulatory team. You will own client engagements and drive regulatory projects, including IDMP data transformation, PMS/RIM integration, and RFP contributions. Expect a mix of consultancy delivery, business development, and mentoring junior staff.

Fluency in English is required; a second language (German, Danish, Italian, or French) is desirable. Travel up to 20% is expected as part of a multinational team.

Competenze

Bachelor’s degree in Pharmaceutical Compliance or Regulation; relevant consulting/industry experience welcomed.
Significant experience in Regulatory Affairs within Life Sciences/pharma.
Experience in IDMP and related data transformation, PMS, and XEVMPD.
Proven consulting experience, ideally in a large life sciences-focused firm.
Familiarity with PMS, Postman API, and RIM systems is an asset.

Mansioni

Own client engagements and manage specific Regulatory Affairs projects.
Contribute to business development, presales and RFP delivery.
Lead project delivery in advisory roles and mentor junior consultants.

Conoscenze

Regulatory Affairs

Consulting

Project leadership

Business development

Client relations

Documentation

Formazione

Bachelor’s degree in Pharmaceutical Compliance or Regulation

Masters degree (preferred)

Strumenti

Power BI

Postman API

RIM systems

Python scripting

Descrizione del lavoro

Fluency in English is required; a second language (German, Danish, Italian, or French) is desirable. Travel up to 20% is expected as part of a multinational team.

Ottieni la revisione del curriculum gratis e riservata.

o trascina qui il file.