Clinical Research Coordinator - Experienced

NovoBliss Research®️ Private Limited; Ahmedabad District; On-site; INR 350,000 - 550,000; Full time

Job summary

NovoBliss Research Private Limited in Ahmedabad, India, seeks a Clinical Research Coordinator to manage studies end-to-end on-site. You will recruit and screen participants, oversee consent, maintain study documentation, and ensure adherence to protocols and regulatory requirements.

Responsibilities include data collection, progress monitoring, sponsor communication, and supporting ethics submissions, audits, and QA activities onsite in Ahmedabad.

Qualifications

• Demonstrated clinical research experience including trials and coordination.
• Strong understanding of informed consent and human subject protection.
• Ability to interpret study protocols, SOPs, and regulatory requirements.
• Solid data collection, documentation and basic data analysis skills.
• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, or related field.
• Knowledge of GCP, ICH guidelines, and local regulatory frameworks (CDSCO).
• Excellent organizational and communication skills; on-site Ahmedabad teammate.

Responsibilities

• Coordinate clinical studies from initiation to close-out.
• Recruit, screen, and schedule study participants.
• Oversee informed consent procedures and study documentation.
• Collect and enter data; monitor study progress and safety.
• Communicate with investigators and sponsors; support ethics submissions.
• Assist audits and quality assurance activities; ensure regulatory compliance.
• Work on-site in Ahmedabad; collaborate with multidisciplinary teams.

Skills

Clinical research experience

Informed consent processes

Regulatory knowledge (GCP/ICH/CDSCO)

Study protocol interpretation

Data collection and analysis basics

Team collaboration and communication

On-site coordination in Ahmedabad

Education

Bachelor’s or Master’s degree in Life Sciences/Healthcare

Job description

Company Description NovoBliss Research® Private Limited, based in Ahmedabad, India, is a CDSCO-registered and ISO 9001:2015 certified Contract Research Organization specializing in scientifically validated clinical safety and efficacy studies for consumer healthcare products. The organization conducts studies across diverse sectors, including nutraceuticals, pharmaceuticals, cosmetics, dental, OTC, and personal healthcare products. The company is committed to advancing global clinical research through scientific excellence, innovation, and integrity. Robust study design, streamlined data collection, and insightful analysis support its focus on precise, efficient, and safe research outcomes.

Role Description The Clinical Research Coordinator is a full-time, on-site role based in Ahmedabad. This position involves coordinating and managing clinical studies from initiation to close-out, including participant recruitment, screening, and scheduling. The coordinator will oversee informed consent procedures, maintain study documentation, and ensure adherence to study protocols and regulatory requirements. Daily responsibilities include data collection and entry, monitoring study progress, communicating with investigators and sponsors, and assisting with ethics committee submissions. The role also requires ensuring participant safety, resolving operational issues, and supporting audits and quality assurance activities.

Qualifications

• Demonstrated clinical research experience, including exposure to clinical trials and study coordination.
• Strong understanding of informed consent processes and ethical guidelines in human subject research.
• Ability to interpret and implement study protocols, SOPs, and regulatory requirements.
• Solid research skills, including data collection, documentation, and basic data analysis.
• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, or a related healthcare field.
• Knowledge of GCP, ICH guidelines, and local regulatory frameworks (e.g., CDSCO requirements).
• Excellent organizational, time management, and communication skills.
• Attention to detail, ability to work collaboratively with multidisciplinary teams, and readiness to work on-site in Ahmedabad.