Clinical Study Specialist: Accelerate Global Trials
Behavioral Health Market Context
Apply Nowvia Learn4Good
Job Description
on patient outcomes? We’re looking for a highly organized, detail-driven Clinical Study Specialist (CSS) to support the execution of innovative clinical programs across global teams.
In this role, you’ll be at the operational heart of clinical trials—collaborating with cross-functional teams, supporting study execution, and ensuring everything runs smoothly from start-up through close-out.
What You’ll Do
As a Clinical Study Specialist, You Will
• 📊 Deliver clear, actionable reports and metrics to support study oversight
• 📅 Coordinate and manage clinical study team meetings (agendas, materials, minutes)
• 🔍 Support feasibility assessments and site selection activities
• 📄 Assist in the review and management of key study documents (ICFs, CRFs, etc.)
• 📚 Maintain study manuals, reference binders, and version-controlled documentation
• 🎓 Prepare materials for investigator meetings and training sessions
• 🚀 Track site activation, enrollment, and monitoring progress—flagging risks early
• 🌐 Maintain investigator/site data and support clinical trial registry updates
• 🗂️ Reconcile and maintain Trial Master File (TMF) documentation
• 🤝 Coordinate with sites, vendors, and internal stakeholders
• 📈 Contribute to data review processes, including Blind Data Review Meetings
• 🔄 Track study close-out activities and ensure compliance
• 💡 Identify and recommend process improvements
Note:
Up to 25% travel may be required.
What You Bring
Required
• Bachelor’s degree (or equivalent) with 2+ years of relevant industry experience OR advanced degree with 1–2 years of experience
• Strong attention to detail and ability to manage multiple priorities
• Excellent communication and relationship-building skills
• Problem-solving mindset with a proactive approach
• Familiarity with clinical development processes and medical terminology
• Working knowledge of ICH/GCP guidelines
Technical Skills
• Experience with clinical systems (CTMS, EDC, IWRS/IVRS)
• Proficiency in Microsoft tools (Teams, Office, Project, SharePoint)
Why Join Us?
• 🌍 Work on global, impactful clinical programs
• 🤝 Collaborate with experienced and supportive teams
• 📈 Grow your career in a fast-paced, innovative environment
• 🧠 Contribute ideas that shape processes and improve outcomes
Ready to Make an Impact?
If you’re a proactive, detail-oriented professional who thrives in a collaborative clinical environment, we’d love to hear from you.
👉 Apply now and help bring life-changing therapies to patients worldwide.
#kpslife#J-18808-Ljbffr
In this role, you’ll be at the operational heart of clinical trials—collaborating with cross-functional teams, supporting study execution, and ensuring everything runs smoothly from start-up through close-out.
What You’ll Do
As a Clinical Study Specialist, You Will
• 📊 Deliver clear, actionable reports and metrics to support study oversight
• 📅 Coordinate and manage clinical study team meetings (agendas, materials, minutes)
• 🔍 Support feasibility assessments and site selection activities
• 📄 Assist in the review and management of key study documents (ICFs, CRFs, etc.)
• 📚 Maintain study manuals, reference binders, and version-controlled documentation
• 🎓 Prepare materials for investigator meetings and training sessions
• 🚀 Track site activation, enrollment, and monitoring progress—flagging risks early
• 🌐 Maintain investigator/site data and support clinical trial registry updates
• 🗂️ Reconcile and maintain Trial Master File (TMF) documentation
• 🤝 Coordinate with sites, vendors, and internal stakeholders
• 📈 Contribute to data review processes, including Blind Data Review Meetings
• 🔄 Track study close-out activities and ensure compliance
• 💡 Identify and recommend process improvements
Note:
Up to 25% travel may be required.
What You Bring
Required
• Bachelor’s degree (or equivalent) with 2+ years of relevant industry experience OR advanced degree with 1–2 years of experience
• Strong attention to detail and ability to manage multiple priorities
• Excellent communication and relationship-building skills
• Problem-solving mindset with a proactive approach
• Familiarity with clinical development processes and medical terminology
• Working knowledge of ICH/GCP guidelines
Technical Skills
• Experience with clinical systems (CTMS, EDC, IWRS/IVRS)
• Proficiency in Microsoft tools (Teams, Office, Project, SharePoint)
Why Join Us?
• 🌍 Work on global, impactful clinical programs
• 🤝 Collaborate with experienced and supportive teams
• 📈 Grow your career in a fast-paced, innovative environment
• 🧠 Contribute ideas that shape processes and improve outcomes
Ready to Make an Impact?
If you’re a proactive, detail-oriented professional who thrives in a collaborative clinical environment, we’d love to hear from you.
👉 Apply now and help bring life-changing therapies to patients worldwide.
#kpslife#J-18808-Ljbffr
Qualifications
- •Up to 25% travel may be required
- •Bachelor’s degree (or equivalent) with 2+ years of relevant industry experience OR advanced degree with 1–2 years of experience
- •Strong attention to detail and ability to manage multiple priorities
- •Excellent communication and relationship-building skills
- •Problem-solving mindset with a proactive approach
- •Familiarity with clinical development processes and medical terminology
- •Working knowledge of ICH/GCP guidelines
- •Experience with clinical systems (CTMS, EDC, IWRS/IVRS)
- •Proficiency in Microsoft tools (Teams, Office, Project, SharePoint)
Benefits
Responsibilities
- •In this role, you’ll be at the operational heart of clinical trials—collaborating with cross-functional teams, supporting study execution, and ensuring everything runs smoothly from start-up through close-out
- •As a Clinical Study Specialist, You Will
- •📊 Deliver clear, actionable reports and metrics to support study oversight
- •📅 Coordinate and manage clinical study team meetings (agendas, materials, minutes)
- •🔍 Support feasibility assessments and site selection activities
- •📄 Assist in the review and management of key study documents (ICFs, CRFs, etc.)
- •📚 Maintain study manuals, reference binders, and version-controlled documentation
- •🎓 Prepare materials for investigator meetings and training sessions
- •🚀 Track site activation, enrollment, and monitoring progress—flagging risks early
- •🌐 Maintain investigator/site data and support clinical trial registry updates
- •🗂️ Reconcile and maintain Trial Master File (TMF) documentation
- •🤝 Coordinate with sites, vendors, and internal stakeholders
- •📈 Contribute to data review processes, including Blind Data Review Meetings
- •🔄 Track study close-out activities and ensure compliance
- •💡 Identify and recommend process improvements
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