Location: Guwahati, Assam
Position: Clinical Research Coordinator
Company: InfoClin Consultancy
Joining: Immediate joiner preferred
About InfoClin Consultancy
At InfoClin Consultancy, we are dedicated to advancing healthcare through high-quality clinical research services. With a strong focus on ethics, regulatory compliance, and patient safety, we collaborate with leading hospitals, research institutions, and pharmaceutical companies to deliver innovative clinical trial solutions. Our team comprises skilled professionals who are passionate about contributing to the growth of evidence-based medicine.
We now invite motivated individuals with a background in pharmaceutical sciences to join our team as Clinical Research Coordinators (CRC) at our Guwahati, Assam office. This role offers a unique opportunity to work in a professional and supportive environment where innovation and scientific rigor are highly valued.
Job Overview
The Clinical Research Coordinator (CRC) plays a vital role in the successful execution of clinical trials. Acting as the link between investigators, sponsors, ethics committees, and patients, the CRC ensures that each study is conducted efficiently, ethically, and in strict compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements.
This position demands not only technical knowledge but also a high level of organizational skills, attention to detail, and the ability to communicate effectively with multiple stakeholders. By joining InfoClin, you will contribute directly to the development of new therapies that have the potential to improve patient care and health outcomes.
Key Responsibilities
As a Clinical Research Coordinator, your role will involve a wide range of responsibilities, including but not limited to:
- Study Coordination: Manage and oversee the day-to-day operations of assigned clinical trials, ensuring smooth conduct from initiation to close-out.
- Patient Management: Assist in patient recruitment, screening, obtaining informed consent, and maintaining follow-up visits in line with study protocols.
- Data Collection & Documentation: Ensure accurate and timely data entry, query resolution, and maintenance of essential study documents such as source notes, case report forms (CRFs), and investigator files.
- Regulatory Compliance: Maintain adherence to ICH-GCP guidelines, institutional SOPs, and study-specific protocols. Support submission to ethics committees and handle regulatory correspondence.
- Collaboration: Act as a key liaison between investigators, sponsors, monitors, and other stakeholders involved in the trial.
- Monitoring & Reporting: Track patient progress, report adverse events, and ensure timely communication of study updates.
- Audit & Inspection Readiness: Prepare study sites for audits and inspections by maintaining complete and accurate documentation.
Candidate Profile
We are looking for dynamic and detail-oriented professionals with the following qualifications:
- Education: M. Pharm / B. Pharm (mandatory).
- Experience: Minimum of 1–2 years of proven experience working as a Clinical Research Coordinator in a hospital, CRO, or research organization.
- Preferred: Immediate joiners who are already familiar with trial site operations.
- Skills & Attributes:
- Strong understanding of clinical research protocols and regulatory frameworks.
- Working knowledge of ICH-GCP guidelines and ethical principles.
- Excellent organizational, interpersonal, and problem-solving abilities.
- Effective communication skills to coordinate with diverse stakeholders.
- Ability to manage time effectively and multitask under strict deadlines.
Benefits of Joining InfoClin
- Opportunity to work with a growing consultancy that values professionalism, ethics, and innovation.
- Hands-on exposure to multiple therapeutic areas and clinical research projects.
- Supportive work culture that encourages learning, development, and career progression.
- Chance to be part of meaningful research that directly impacts patient lives and healthcare outcomes.
Application Process
If you are passionate about clinical research and meet the qualifications, we encourage you to apply. Please send your updated CV with the subject line:
“Application for Clinical Research Coordinator – Guwahati”
Why Choose This Role?
Becoming a Clinical Research Coordinator at InfoClin Consultancy is not just another job—it’s a stepping stone into the ever-growing clinical research industry. With increasing demand for skilled CRCs in India and abroad, this role offers you professional stability, global exposure, and the chance to contribute to the discovery of new treatments and therapies. If you’re looking to advance your career while making a meaningful impact in the healthcare sector, this is the perfect opportunity for you.
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