Syneos Health
life sciences
SrCRA6monthFreelancer
“SrCRA- 6 month Freelancer at Syneos Health. Skills: Clinical Monitoring, Site Management, ICH-GCP. Monitor clinical studies. Ensure protocol compliance”
What You'll Achieve.
Accelerate customer success; Navigate complexity; Anticipate change; Accelerate progress; Achieve goals; Meet targets
Industry & Context.
Moderate level of critical thinking skills
Travel up to 75%
What They're Looking For.
Must Have
Knowledge of Good Clinical Practice/ICH Guidelines, Knowledge of other applicable regulatory requirements, Demonstrate good computer skills, Embrace new technologies, Ability to manage required travel of up to 75%
What You'll Do.
Monitor clinical studies
Ensure protocol compliance
Evaluate site performance
Communicate serious issues
Verify informed consent
Assess site processes
Conduct Source Document Review
Manage investigational product
Review Investigator Site File
Support subject recruitment
Enter data into tracking systems
Manage site-level activities
Provide site guidance
Support audit preparation
Perform training visits
Participate in business development
Support study lifecycle
Identify out of scope activities
Suggest potential sites
Identify operational efficiencies
Develop informed consent forms
Participate in bid defense meetings
How You'll Work.
Team & Collaboration
Collaborate with project team; Collaborate with Central Monitoring Associate; Collaborate with Sponsor; Collaborate with other affiliates; Collaborate with medical science liaisons; Collaborate with local country staff
Communication Scope
Excellent communication skills; Excellent presentation skills
Process & Methodology
Manage project objectives, Manage project deliverables, Manage project timelines
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