Empregos para ich em Coimbra

### **RA Technician*** Country: PORTUGAL* Workplace:* Type of contract: Permanent* Date publish: 23/03/2026* Timetable:* Vacancies: 1#### **Job description**At SF CDMO, we are looking for an individual eager to grow within our RA team in Castanheira do Ribatejo, Lisbon.RESPONSIBILITIES:Support the global review and analysis of technical documentation,...

Bluepharma is seeking a Formulation Scientist to lead oral solids development within a QbD framework. You will work on formulation and process development, ensuring compliance with GMP/ICH and robust documentation. Responsibilities include planning experiments, scaling up for manufacturing for pre-clinical and clinical trials, and collaborating across teams...

Syneos Health is seeking a Sponsor Dedicated Medical Writer II/Sr for remote-based work in Portugal. The role focuses on leading medical writing deliverables across studies, coordinating with data management, biostatistics, regulatory and medical affairs teams. Strong knowledge of FDA/ICH guidelines and AMA style is required. Responsibilities include...

Who We Are Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20 pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end-to-end clinical trial solutions across all phases, offering Phase I-IV and...

Location: Portugal (home-based) Contract type: Freelance FTE: 0.5 - 0.75 Start: immediately Duration: around 4 month About the Role We are looking for a Freelance Site Activation Specialist based in Portugal to support country-level clinical trial start-up and site management activities. This role focuses on feasibility, site identification,...

Syneos Health is seeking a Sponsor Dedicated Medical Writer II/Sr for remote-based work in Portugal. The role focuses on leading medical writing deliverables across studies, coordinating with data management, biostatistics, regulatory and medical affairs teams.Strong knowledge of FDA/ICH guidelines and AMA style is required. Responsibilities include drafting...

At Medinfar, your work has a real impact: helping to bring healthcare to everyone. Join a team driven by purpose, innovation, ethics and sustainability. **Together, we take better care.** **Your role at Medinfar**: The **_Qualification and CSV Technician_** plays a critical role in GMP operations by supporting the qualification of equipment, facilities,...

At Medinfar, your work has a real impact: helping to bring healthcare to everyone. Join a team driven by purpose, innovation, ethics and sustainability.👉 Together, we take better care.Your role at Medinfar:The Qualification and CSV Technician plays a critical role in GMP operations by supporting the qualification of equipment, facilities, utilities and...