Description
Syneos Health is seeking a Site Activation Specialist II to join their team in Madrid. As a Site Activation Specialist II, you will be responsible for ensuring quality deliverables at the country level, following project requirements and applicable country rules.
Job Responsibilities
- Responsible for quality deliverables at the country level, following project requirements and applicable country rules with moderate oversight from the SSU Country Manager.
- Monitor basic financial aspects of the project and track milestone progress in real-time.
- Review and comply with Standard Operating Procedures (SOPs) and Work Instructions (WI) in a timely manner.
- Support continuous improvement of quality in all Site Start-Up (SSU) components at the country level.
- Ensure all relevant documents are submitted to the Trial Master File (TMF) as per Company SOP/Sponsor requirements.
- Act as a liaison and facilitator between investigational sites and functional leads for related tasks and/or issues.
- Provide support with site selection, contract and budget negotiations, and local regulatory authority submissions.
Qualifications
- Bachelor's degree
- Over 2 years of experience in a similar role
- 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
What We Offer
- Opportunity to work with a leading life sciences services organization
- Collaborative and dynamic work environment
- Professional development and growth opportunities
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