Job Opportunity: Clinical Research Coordinator (CRC) at Shivensis Research

Job Summary
Shivensis Research is seeking two dedicated and detail-oriented Clinical Research Coordinators (CRC) to join our team in Delhi/Gurugram. This position is perfect for professionals with a background in life sciences, pharmacy, or biotechnology who are eager to advance their careers in clinical trial management, Good Clinical Practice (GCP) compliance, and patient care. In this role, you will be instrumental in ensuring the smooth execution of neurology-focused clinical studies, working closely with investigators, CROs, and regulatory bodies to maintain the highest standards of research integrity.

Job Overview

• Position: Clinical Research Coordinator (CRC)
• Company: Shivensis Research
• Location: Delhi / Gurugram
• Employment Type: Full-time
• Vacancies: 2
• Experience Required: 1–2 years (Experience in Neurology clinical trials is highly preferred)
• Languages: Proficiency in Hindi and English is required

Responsibilities

As a Clinical Research Coordinator, your primary goal is to ensure that clinical trials are conducted efficiently and ethically. Your daily responsibilities will include:

• Trial Operations: Managing the day-to-day operations of clinical trial sites to ensure protocols are followed precisely.
• Patient Management: Assisting the Principal Investigator (PI) with patient recruitment, the informed consent process, and patient screening and enrollment.
• Compliance: Ensuring all research activities adhere to ICH-GCP guidelines, study protocols, and local regulatory requirements.
• Safety Monitoring: Diligently monitoring and reporting all Adverse Events (AE) and Serious Adverse Events (SAE) to relevant stakeholders.
• Collaboration: Acting as a bridge between the clinical site, Contract Research Organizations (CROs), and the Ethics Committee (EC).
• Regulatory Support: Assisting during site monitoring visits, audits, and regulatory inspections.
• Reporting: Preparing and submitting accurate, timely clinical trial reports and site updates.

Requirements

We are looking for candidates who possess a blend of technical knowledge and strong interpersonal skills:

• Education: A Bachelor’s or Master’s degree in Life Sciences, Pharmacy (B.Pharm/M.Pharm), or Biotechnology.
• Experience: 1–2 years of relevant experience in clinical trial coordination.
• Core Knowledge: A firm grasp of Good Clinical Practice (GCP) guidelines and a deep understanding of the clinical trial lifecycle.
• Soft Skills: Exceptional communication and organizational skills, with the ability to coordinate effectively across multidisciplinary teams.
• Specialization: Previous experience or academic focus within the field of Neurology is a significant advantage.

Benefits

Shivensis Research offers a supportive environment designed to foster your professional development within the healthcare sector:

• Competitive Compensation: An estimated salary of ₹2.5 – ₹4.5 LPA, commensurate with experience and industry standards.
• Skill Development: Gain hands-on exposure to complex neurology clinical trials and regulatory audit procedures.
• Career Advancement: This role serves as an ideal foundation for those looking to transition into roles such as Clinical Research Associate (CRA), Clinical Trial Manager, or Regulatory Affairs Specialist.
• Professional Networking: Opportunity to work directly with experienced investigators and major CROs, expanding your industry footprint.

How to Apply

If you are a motivated professional looking to make a meaningful impact in clinical research, we would love to hear from you. Please submit your updated resume and a cover letter detailing your relevant experience and qualifications to the Shivensis Research HR department via our official company career portal or by sending your application to our designated recruitment email address.

Shivensis Research is an equal opportunity employer committed to fostering a diverse and professional workplace.