Description
Syneos Health is seeking a Site Activation Specialist II to join their Clinical Solutions team. The successful candidate will be responsible for ensuring quality deliverables at the country level, following project requirements and applicable country rules. Key responsibilities include:
- Monitoring project timelines and milestones, and escalating issues as needed
- Reviewing and complying with Standard Operating Procedures (SOPs) and Work Instructions (WI)
- Supporting continuous improvement of quality in Site Start-Up (SSU) components
- Preparing and submitting regulatory authority applications and other local regulatory authorities or hospital approval submissions
- Acting as a liaison and facilitator between investigational sites and functional leads
The ideal candidate will have:
- A Bachelor's Degree
- Detailed understanding of clinical trial process across Phases II-IV and ICH GCP
- Ability to understand clinical protocols and associated study specifications
- Strong organizational skills with ability to handle multiple tasks effectively
- Strong written and verbal communication and interpersonal skills
Syneos Health offers a range of benefits, including career development and progression opportunities, supportive and engaged line management, technical and therapeutic area training, and a total rewards program.