Clinical Trials Assistant (CTA)

Sunfox Technologies
πŸ‘œ 0 - 3 years
πŸ“ Dehradun
πŸ’Ό Full-Time
Posted on May 31, 2026

Brief Summary:

Sunfox Technologies is actively hiring a Clinical Trials Assistant (CTA) for its Dehradun office.

This is an excellent opportunity for Freshers and Early-Career Professionals who want to build a rewarding career in Clinical Research, Clinical Trial Management, TMF Management, Regulatory Compliance, and Healthcare Innovation.

Job Description:

πŸš€ WE’RE HIRING | Clinical Trials Assistant (CTA) | Sunfox Technologies | Dehradun πŸš€

Are you looking to start your career in Clinical Research, Clinical Trials, Regulatory Documentation, and Clinical Operations? πŸ§ͺπŸ“‹βœ¨

πŸ“’ Sunfox Technologies is actively hiring a Clinical Trials Assistant (CTA) for its Dehradun office.

This is an excellent opportunity for Freshers and Early-Career Professionals who want to build a rewarding career in Clinical Research, Clinical Trial Management, TMF Management, Regulatory Compliance, and Healthcare Innovation.

If you are passionate about clinical trials, research operations, trial documentation, and healthcare technology, this opportunity can provide valuable industry exposure and long-term career growth.

🏒 Company: Sunfox Technologies
🌐 Website: https://sunfox.in
🏭 Industry: Healthcare Technology / Clinical Research / Medical Devices
πŸ‘‰ Role: Clinical Trials Assistant (CTA)
πŸ’Ό Experience: 0–3 Years
πŸŽ“ Qualification: B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Life Sciences, Nursing, or Related Healthcare Fields
πŸ“ Location: Dehradun, Uttarakhand
🏒 Work Mode: On-site
πŸ•’ Employment Type: Full-Time, Permanent
πŸ’° Salary: β‚Ή15,000 – β‚Ή18,000 per Month

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πŸ’Ό Short Job Description
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Sunfox Technologies is seeking motivated candidates to support clinical research operations and clinical trial activities.

The selected candidate will assist in clinical study coordination, Trial Master File (TMF) management, regulatory documentation, site communication, compliance activities, and clinical trial execution.

This role offers excellent exposure to:
βœ… Clinical Trial Management
βœ… Clinical Research Operations
βœ… TMF Management
βœ… Regulatory Documentation
βœ… Clinical Site Coordination
βœ… Healthcare & Medical Device Research

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πŸ”§ Key Responsibilities
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βœ” Assist in planning, coordinating, and executing clinical trials from initiation through close-out
βœ” Support Clinical Research Associates (CRAs) and Clinical Trial Managers in daily study operations
βœ” Maintain and organize Trial Master Files (TMF) according to regulatory requirements
βœ” Track study timelines, site activities, and clinical data collection progress
βœ” Coordinate with investigators, research sites, and vendors to ensure smooth study execution
βœ” Prepare and review clinical trial documents, protocols, reports, and regulatory submissions
βœ” Ensure compliance with ICH-GCP guidelines and applicable regulatory standards
βœ” Support audit readiness and inspection preparation activities
βœ” Manage study supplies, communication records, and tracking logs

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πŸ›  Required Skills & Qualifications
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πŸŽ“ Educational Qualification
βœ… Bachelor’s Degree in Life Sciences
βœ… Master’s Degree in Life Sciences
βœ… Bachelor of Pharmacy (B.Pharm)
βœ… Master of Pharmacy (M.Pharm)
βœ… Pharm.D
βœ… Nursing Degree
βœ… Related Healthcare or Clinical Research Qualifications

πŸ’Ό Experience Requirements
βœ… 0–3 years of experience in Clinical Research or Clinical Trials
βœ… Freshers with relevant internships in Clinical Research are welcome to apply

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🎯 Required Skills
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βœ… Understanding of Clinical Trial Processes
βœ… Knowledge of ICH-GCP Guidelines
βœ… Strong Documentation and Organizational Abilities
βœ… Excellent Communication and Coordination Skills
βœ… Proficiency in Microsoft Word, Excel, and PowerPoint
βœ… Attention to Detail and Compliance-Focused Mindset

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⭐ Preferred Skills
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βœ” Experience with TMF Management Systems
βœ” Exposure to Clinical Trial Software Platforms
βœ” Understanding of Regulatory Submissions
βœ” Clinical Documentation Management Experience
βœ” Ability to Work in a Fast-Paced Clinical Research Environment

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✨ Salary & Benefits
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πŸ’° Salary: β‚Ή15,000 – β‚Ή18,000 per Month

🎁 Employee Benefits
✨ Provident Fund (PF)
✨ Paid Time Off
✨ Leave Encashment
✨ Professional Growth Opportunities in Clinical Research
✨ Exposure to Clinical Trial Operations and Regulatory Processes
✨ Hands-on Experience with Trial Documentation and Compliance Activities
✨ Learning Opportunities in a Growing Healthcare Technology Organization

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🏒 About Sunfox Technologies
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Sunfox Technologies is a rapidly growing healthcare technology company focused on innovation and improving healthcare outcomes through advanced medical technologies and research-driven solutions.

The company works at the intersection of healthcare, technology, clinical research, and medical innovation, helping improve patient care through cutting-edge healthcare solutions.

πŸš€ Core Focus Areas:
βœ… Healthcare Technology Innovation
βœ… Clinical Research & Clinical Trials
βœ… Medical Device Development
βœ… Digital Health Solutions
βœ… Regulatory & Compliance Excellence
βœ… Patient-Centric Healthcare Solutions

Sunfox Technologies provides an excellent platform for aspiring clinical research professionals to gain practical industry exposure while working on meaningful healthcare initiatives.

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πŸš€ Career Growth Opportunities
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This role serves as an excellent entry point for professionals aspiring to become:

βœ… Clinical Research Associate (CRA)
βœ… Clinical Trial Coordinator
βœ… Clinical Trial Manager
βœ… Regulatory Affairs Associate
βœ… Clinical Operations Specialist

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πŸ“© Apply Now
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Interested candidates can apply by sending their updated resume to:
πŸ“§ careers@sunfox.in

πŸ’¬ Join WhatsApp Group:
Join Now

⚑ If you’re looking to launch your career in Clinical Research, Clinical Trials, Regulatory Affairs, and Clinical Operations, Sunfox Technologies offers an excellent opportunity to gain hands-on experience, develop industry-relevant skills, and grow within the healthcare and medical technology sector.

Required Skills:

βœ… Understanding of Clinical Trial Processes βœ… Knowledge of ICH-GCP Guidelines βœ… Strong Documentation and Organizational Abilities βœ… Excellent Communication and Coordination Skills βœ… Proficiency in Microsoft Word, Excel, and PowerPoint βœ… Attention to Detail and Compliance-Focused Mindset

About Sunfox Technologies

Sunfox Technologies is a rapidly growing healthcare technology company focused on innovation and improving healthcare outcomes through advanced medical technologies and research-driven solutions.

The company works at the intersection of healthcare, technology, clinical research, and medical innovation, helping improve patient care through cutting-edge healthcare solutions.

πŸš€ Core Focus Areas:

βœ… Healthcare Technology Innovation
βœ… Clinical Research & Clinical Trials
βœ… Medical Device Development
βœ… Digital Health Solutions
βœ… Regulatory & Compliance Excellence
βœ… Patient-Centric Healthcare Solutions

Sunfox Technologies provides an excellent platform for aspiring clinical research professionals to gain practical industry exposure while working on meaningful healthcare initiatives.

βœ‰ How to Apply / Contact Info

To apply for this position or make inquiries, please reach out directly to the employer at the contact email address below:

careers@sunfox.in
βœ” Verified