eTMF Specialist I – Regulatory & TMF (Hybrid)

CTI; Lisboa; Ibrido; EUR 40.000 - 68.000; Tempo pieno

Descrizione del lavoro

CTI Clinical Trial and Consulting Services is a global CRO focused on advancing treatments for chronically and critically ill patients. We are seeking a Regulatory and TMF coordinator to support regulatory documentation and TMF management.

Ideal candidate has a Bachelor’s degree in allied health and 2–4 years’ pharmaceutical or CRO experience in regulatory affairs and TMF activities. This role offers a collaborative, team-based environment with opportunities for growth and international exposure.

Competenze

• 2-4 years pharmaceutical or CRO Clinical Regulatory and/or document / TMF management experience

Formazione

Bachelor's degree in allied health field such as nursing, pharmacy, or health science or equivalent relevant experience

Descrizione del lavoro

CTI Clinical Trial and Consulting Services is a global CRO focused on advancing treatments for chronically and critically ill patients. We are seeking a Regulatory and TMF coordinator to support regulatory documentation and TMF management.

Ideal candidate has a Bachelor’s degree in allied health and 2–4 years’ pharmaceutical or CRO experience in regulatory affairs and TMF activities. This role offers a collaborative, team-based environment with opportunities for growth and international exposure.