Country Approval Specialist

📋 Description

• Prepare, review, and coordinate local Ethics Committee submissions under guidance and in accordance
• Support the preparation of local Ministry of Health or other regulatory submissions, where
• Coordinate with internal functional teams to align site start-up activities, submission activities
• Work toward established country and site submission cycle-time targets.
• Communicate with investigators, where required, regarding submission-related activities.
• Serve as a country-level contact for selected ethics or regulatory submission activities, as

🎯 Requirements

• Bachelor’s degree or equivalent qualification, preferably in a relevant scientific, healthcare
• 0–2 years of relevant experience, or an equivalent combination of education, training, and directly
• Strong written and verbal communication skills, with good English language and grammar proficiency.
• Excellent interpersonal and collaboration skills, with the ability to work effectively with
• Strong attention to detail and a commitment to accurate, high-quality documentation.
• Good negotiation, organizational, and planning skills.

🎁 Benefits

• Fully remote work arrangement within India.
• Full-time position with a standard Monday–Friday schedule.
• Opportunity to gain hands-on experience in clinical research, regulatory submissions, and country
• Exposure to global study teams and cross-functional collaboration.
• Professional development and opportunities to build expertise in clinical trial operations and
• Inclusive and collaborative work environment focused on innovation, scientific advancement, and