Clinical Support Specialist II Vacancy at Syneos Health – Apply Now

Syneos Health is hiring for the position of Clinical Support Specialist II at its Hyderabad location. This opportunity is ideal for professionals with 1 to 2 years of clinical operations experience who are looking to grow their careers in clinical research support, documentation management, and operational coordination. The role plays a critical part in supporting CRAs, regulatory teams, and project stakeholders to ensure smooth execution of clinical trials.

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🏢 About the Employer

Syneos Health is a global clinical research and biopharmaceutical solutions organization supporting the full lifecycle of drug development. The company integrates clinical operations, data management, regulatory support, and technology‑enabled solutions to deliver high‑quality clinical trials worldwide. Working at Syneos Health provides exposure to global studies, advanced technologies, and regulated clinical environments.

📊 Job Summary

• Company Name: Syneos Health
• Job Role: Clinical Support Specialist II
• Employment Type: Full‑Time
• Experience Required: 1 to 2 Years
• Functional Area: Clinical Operations / Clinical Support
• Job Location: Hyderabad

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📋 Key Duties

• Providing operational and administrative support to one or more clinical functionsCoordinating documentation and communications, including:
• Managing shared mailboxes
• Organizing project files
• Tracking action items and follow‑ups with cross‑functional teams
• Entering, maintaining, and reconciling data in approved clinical and project tracking systemsSupporting timeline and milestone trackingPerforming document management activities, including:
• Document creation, compilation, formatting, and version control
• Quality control (QC) checks
• Coordinating translation of documents using approved vendors and systems
• Utilizing AI‑enabled tools, dashboards, and automated reports for organizational and analytical support
• Supporting Trial Master File (TMF) filing and ensuring inspection‑ready documentation
• Delivering high‑quality outputs in alignment with project requirements and country‑specific regulations
• Ensuring compliance with SOPs, Work Instructions (WIs), and training requirements
• Maintaining accurate timesheet reporting
• Monitoring workload, scope, project hours, and budgeted effort, and escalating issues when required
• Maintaining ongoing awareness of clinical research practices through required training

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🎓 Eligibility Requirements

Candidates applying for this role should meet the following criteria:

• Bachelor’s degree or an equivalent combination of education, training, and experience
• 1 to 2 years of experience in clinical operations or a related function
• Experience providing operational and administrative support to:
  • Clinical Research Associates (CRAs)
  • Country Regulatory Specialists within site activation and regulatory submission activities

🧠 Core Skills

The following skills are essential for success in this role:

• Good understanding of clinical research, drug development, and clinical trial processes (startup, maintenance, closeout)
• Demonstrated knowledge of clinical operations and trial workflows
• Strong written and verbal communication skills in English
• Excellent documentation and organizational skills with attention to detail
• Effective problem‑solving abilities and proactive approach to improving efficiency and quality
• Ability to manage competing priorities in a fast‑paced environment
• Proficiency in Microsoft Office Suite (Outlook, Word, Excel, PowerPoint, Publisher)
• Willingness and ability to learn and adopt new technologies, including AI‑enabled tools and dashboards
• Ability to work independently and collaboratively within cross‑functional teams
• Quality‑driven mindset across all assigned activities
• Flexibility and adaptability in a changing clinical research environment

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⭐ Job summary

The Clinical Support Specialist II role is a critical backbone position within clinical operations. Professionals in this role ensure smooth coordination of documentation, timelines, and compliance activities that support CRAs and regulatory teams. The role offers excellent exposure to TMF processes, AI‑supported clinical workflows, and global trial operations, making it a strong stepping stone to advanced clinical operations or regulatory roles.

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🎯 Suitable Candidates

This opportunity is suitable for:

• Clinical operations professionals with 1–2 years of experience
• Candidates with exposure to TMF, documentation, or site activation support
• Individuals seeking growth in global CRO environments
• Professionals interested in operational excellence within clinical trials

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🎯 Best Fit Candidates

With experience and performance, professionals can progress into roles such as:

• Senior Clinical Support Specialist
• Clinical Trial Assistant (CTA)
• Clinical Operations Associate
• Regulatory or Project Coordination roles

You can explore future growth opportunity in clinical research

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💰 Expected Salary

• ₹4,00,000 – ₹7,00,000 per annum (CTC)
  (Based on industry standards for 1–2 years clinical operations experience)

Actual compensation depends on experience, skill set, and internal policies.

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🔗 Application Link

Interested candidates should apply only through the official company career website using the link provided below.

Important Disclaimer:This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official website before applying.

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