Clinical research co-ordinator

NovoBliss Research®️ Private Limited; Ahmedabad District; On-site; INR 500,000 - 700,000; Full time

Job summary

NovoBliss Research® Private Limited is hiring a Clinical Research Coordinator in Ahmedabad, India. This full-time, on-site role involves planning and executing clinical studies while adhering to strict protocols and regulations.

The ideal candidate has a strong background in clinical research, excellent organizational skills, and is proficient in English. Responsibilities include participant recruitment, study management, and data handling, ensuring compliance with Good Clinical Practice (GCP) guidelines.

Qualifications

• Experience in clinical research and clinical trials.
• Familiarity with regulatory guidelines.
• Ability to implement study protocol requirements.

Responsibilities

• Coordinate participant screening, recruitment, and enrollment.
• Ensure adherence to study protocols and regulatory requirements.
• Maintain accurate source documents and case report forms.

Skills

Clinical research experience

Knowledge of Good Clinical Practice (GCP)

Data collection and documentation

Strong communication skills

Organizational skills

Education

Bachelor’s or Master’s degree in Life Sciences

Clinical research certification

Tools

MS Office

Job description

NovoBliss Research® Private Limited, based in Ahmedabad, India, is a CDSCO-registered and ISO 9001:2015 certified Contract Research Organization (CRO) specializing in scientifically validated clinical safety and efficacy studies for consumer healthcare products. The organization conducts research across multiple sectors, including nutraceuticals, pharmaceuticals, cosmetics, dental, OTC, and personal healthcare products. As a member of the Advertising Standards Council of India (ASCI) and the Indian Society for Clinical Research (ISCR), NovoBliss Research® maintains high ethical and regulatory standards. Founded by Dr. Nayan Patel and Dr. Maheshvari Patel, the company is committed to advancing global clinical research with a strong focus on scientific rigor, innovation, and integrity. Through robust study design, streamlined data collection, and in-depth analysis, NovoBliss Research® delivers precise, efficient, and high-quality research outcomes.

Role Description This is a full-time, on-site Clinical Research Coordinator role based in Ahmedabad. The Clinical Research Coordinator will support the planning, initiation, and execution of clinical studies, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Responsibilities include coordinating participant screening, recruitment, and enrollment; obtaining and documenting informed consent; and scheduling and managing study visits and follow-ups. The role involves maintaining accurate source documents and case report forms, managing study supplies, and assisting with sample collection, processing, and shipment as required. The coordinator will collaborate with investigators, sponsors, and cross-functional teams, support ethics committee submissions, track study timelines, and contribute to data entry, query resolution, and preparation of study reports and documentation.

Qualifications

• Demonstrated experience in clinical research and clinical trials, including familiarity with Good Clinical Practice (GCP) and relevant regulatory guidelines.
• Strong understanding of study protocols and ability to implement protocol requirements consistently during all study phases.
• Hands-on experience with informed consent processes, including explaining study procedures, risks, and benefits to participants and documenting consent accurately.
• Solid research skills, including data collection, documentation, and basic analysis for clinical studies.
• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, or a related healthcare field (clinical research certification is an advantage).
• Excellent organizational and time-management skills, with the ability to manage multiple studies or tasks simultaneously.
• Strong written and verbal communication skills in English; proficiency in local languages is beneficial for participant interaction.
• High attention to detail, integrity in handling confidential data, and a commitment to ethical research conduct.
• Proficiency in basic computer applications (e.g., MS Office) and familiarity with