THE FORCE CT GmbH

• Work in a flexible environment • Collaborate with diverse teams • Adapt to customer needs and problems

• Identify relevant tenders • Develop pricing strategies • Conduct discussions and negotiations with group purchasing organizations (GPOs) • Bring order to a structurally disorganized area

• Navigate challenges in regulatory strategy and life-cycle measures. • Handle complex regulatory topics with ease. • Communicate with health authorities (i.e. PMDA) and clients or partners. • Knowledgeable in regulatory procedures and guidelines in Japan for medicinal products and beyond. • Explore new product types.

• Establish systems and processes for PV activities • Monitor the performance of PV systems • Lead and support PV audits and inspections • Develop PV documentation across the product lifecycle

• Planning, coordination, and execution of medical and scientific research projects • Ensuring Good Clinical Practice (GCP) and regulatory requirements are followed • Assisting in study documentation, data collection, and data management • Coordinating communication between investigators, sponsors, CROs, and study teams • Writing Clinical Study Reports (CSR) and scientific publications • Handling safety case reports and query management