KV Clinical Research Pvt. Ltd. has announced an opening for the position of Clinical Research Coordinator (CRC) for its clinical research operations in Ranchi and Patna. Candidates with pharmaceutical or clinical research qualifications and at least 1 year of clinical research experience are invited to apply.

KV Clinical Research Pvt. Ltd. operates as a Site Management Organization (SMO) supporting clinical research activities. This opportunity can be relevant for B.Pharm, M.Pharm, Pharm.D, Diploma in Clinical Research, and M.Sc Clinical Research candidates looking to build their careers in clinical trial operations and site coordination.

Applicants who meet the eligibility requirements can submit their CV directly to the HR email address provided by the company.

KV Clinical Research CRC Job Overview

About the Clinical Research Coordinator Role

A Clinical Research Coordinator typically supports the day-to-day execution of clinical trials at the investigational site under the supervision of investigators and in accordance with the study protocol and applicable regulatory requirements.

CRC professionals commonly coordinate activities among investigators, study participants, sponsors, CROs, monitors, ethics committees, laboratories, and other stakeholders involved in clinical trials.

For this vacancy, KV Clinical Research specifically states that candidates should have 1+ year of clinical research experience.

Key Responsibilities

Based on standard CRC functions within clinical research sites, responsibilities may include:

• Supporting investigators in the day-to-day coordination of clinical studies.
• Coordinating study participant screening, enrollment, and follow-up activities.
• Maintaining clinical trial documentation and essential study records.
• Supporting informed consent documentation and study-related processes.
• Coordinating scheduled study visits according to the clinical trial protocol.
• Assisting with Case Report Form (CRF/eCRF) completion and study data documentation.
• Coordinating with sponsors, CROs, Clinical Research Associates (CRAs), investigators, and other study stakeholders.
• Supporting monitoring visits, audits, and inspection-readiness activities.
• Tracking study-related documentation and ensuring timely filing.
• Supporting documentation of adverse events and serious adverse events as applicable.
• Following the study protocol, SOPs, Good Clinical Practice (GCP), and applicable regulatory requirements.
• Supporting overall site-level clinical trial execution.

Note: The vacancy notice primarily provides the role, qualifications, locations, and experience requirement. The responsibilities above describe typical CRC activities and should not be interpreted as an exhaustive company-issued job description.

Qualification & Eligibility

Candidates applying for the KV Clinical Research Coordinator vacancy should have one of the qualifications mentioned in the recruitment notice:

• B.Pharm
• M.Pharm
• Pharm.D
• Diploma in Clinical Research
• M.Sc in Clinical Research

Applicants should also have at least 1 year of experience in Clinical Research.

Candidates with exposure to clinical trial documentation, site coordination, GCP, informed consent processes, CRF/eCRF handling, and communication with investigators or CRAs may find these skills relevant to a CRC position.

Experience Required

KV Clinical Research has specifically mentioned:

Experience: 1+ year in Clinical Research

Therefore, this particular Clinical Research Coordinator opening should not be presented as a fresher vacancy. Candidates with one year or more of relevant clinical research experience are the intended applicants based on the recruitment notice.

Job Locations

The CRC vacancies are available at:

Ranchi
Jharkhand, India

Patna
Bihar, India

Candidates should consider their willingness and ability to work at the applicable clinical research site before applying.

Why Consider a Career as a Clinical Research Coordinator?

A Clinical Research Coordinator role provides hands-on exposure to clinical trial execution at the site level. Professionals can develop practical knowledge of clinical study protocols, patient coordination, essential documents, GCP requirements, monitoring activities, CRFs, and clinical trial compliance.

Experience as a CRC may also provide a foundation for future opportunities in areas such as Clinical Operations, Clinical Research Associate (CRA), Site Management, Clinical Trial Assistant, Project Coordination, and other clinical research functions, depending on experience and additional skills.

Salary

The official vacancy notice does not disclose a salary.

For structured-data purposes only, an indicative market estimate of approximately ₹3,00,000–₹5,00,000 per year may be considered for CRC roles with early-career clinical research experience in India. Actual compensation offered by KV Clinical Research may differ depending on experience, location, skills, and company policy.

Candidates should confirm compensation directly with the employer during the recruitment process.

How to Apply for KV Clinical Research CRC Job

Eligible candidates can apply by sending their updated CV/resume to:

Email: hr@kvclinicalresearch.com

Mentioning “Application for Clinical Research Coordinator – Ranchi/Patna” in the email subject can help clearly identify the position being applied for.