Clinical Trial Coordinators Required Hyderabad I’SHNOVA Clinicals

I’SHNOVA Hiring Freshers – Junior Clinical Trial Coordinator | B.Pharm/M.Pharm/MSc Life Sciences | Secunderabad

I’SHNOVA Clinical Trial Company is inviting applications for the position of Junior Clinical Trial Coordinator at its Old Alwal office in Secunderabad. This is a full-time, on-site opportunity specifically open to freshers who have completed B.Pharm, M.Pharm, or MSc Life Sciences. Candidates currently pursuing their degree are not eligible.

This role is ideal for pharmacy and life sciences graduates looking to begin their career in clinical research, clinical trials management, and regulatory-compliant healthcare operations. With structured exposure to patient coordination, clinical data management, and ICH-GCP compliance, this position offers practical entry into the growing clinical research industry.

The offered salary is ₹15,000 per month, and importantly, there are no agreements or employment bonds required.

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Company Overview

I’SHNOVA Clinical Trial Company operates in the field of clinical research and site-level trial management. The organization focuses on conducting ethically compliant and scientifically sound clinical studies in alignment with ICH-GCP guidelines and regulatory requirements.

Clinical trial coordinators form the backbone of any successful clinical research study. They ensure accurate documentation, patient safety, regulatory compliance, and seamless communication between investigators, sponsors, and participants. At I’SHNOVA, fresh graduates are trained in real-time clinical trial processes, making it a valuable starting point for those aspiring to build a career in clinical research, pharmacovigilance, regulatory affairs, or clinical data management.

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Job Role & Responsibilities

As a Junior Clinical Trial Coordinator, you will support ongoing clinical studies at the site level under the supervision of senior clinical research professionals.

Patient Coordination

• Assist in screening potential study participants as per protocol inclusion and exclusion criteria.
• Support patient recruitment activities.
• Coordinate informed consent processes in accordance with ethical guidelines.
• Schedule patient visits and ensure adherence to study timelines.

Data Management

• Enter clinical trial data accurately into Case Report Forms (CRFs) or electronic data capture systems.
• Ensure completeness and accuracy of source documentation.
• Support query resolution and maintain data integrity throughout the study.

Regulatory Compliance

• Ensure study activities comply with ICH-GCP guidelines and approved study protocols.
• Follow standard operating procedures (SOPs) during trial conduct.
• Maintain confidentiality and patient data protection standards.

Documentation & Record Maintenance

• Maintain and update the Investigator Site File (ISF).
• Organize essential regulatory documents and trial-related records.
• Prepare files for audits or internal quality checks.

This position provides foundational exposure to clinical trial operations, regulatory documentation, medical research ethics, and healthcare compliance practices.

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Eligibility / Qualifications

Educational Qualification (Completed Degree Mandatory)

B.Pharm, M.Pharm, MSc Life Sciences

Relevant Specializations: Pharmacology, Pharmaceutics, Clinical Research, Biotechnology, Microbiology, Biochemistry, Life Sciences.

Candidates currently pursuing their degree are not eligible for this full-time position.

Experience

• Freshers are eligible.
• Basic knowledge of clinical research processes and ICH-GCP guidelines is preferred.

Key Skills

• Strong attention to detail and documentation accuracy.
• Good communication skills for patient interaction.
• Basic understanding of clinical trial protocols.
• Ability to maintain organized records and regulatory files.
• Willingness to work in an office-based clinical research environment.

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Location & Salary Details

• Location: Old Alwal, Secunderabad (On-site / Office-based)
• Employment Type: Full-time
• Salary: ₹15,000 per month
• Agreements/Bonds: Not required

This is an entry-level opportunity suited for graduates seeking hands-on experience in clinical trials, site management, and healthcare research operations.

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Application & Selection Process

Interested candidates must email their updated CV or resume to:

Email: employmentishnova@gmail.com

Selection Process

1. Initial Submission – Send resume to the HR department via the mentioned email ID.
2. Eligibility Check – Only candidates who have completed B.Pharm, M.Pharm, or MSc Life Sciences will be shortlisted.
3. Technical Call – Shortlisted candidates will receive communication via email and attend an initial technical discussion.
4. Final Interview – Selected candidates will attend a face-to-face subject interview with the Department Manager at the office.

All official communication will be sent from employmentishnova@gmail.com.

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Frequently Asked Questions (FAQs)

1. Is this role open to freshers?

Yes. This position is specifically designed for fresh pharmacy and life sciences graduates.

2. Are candidates pursuing their degree eligible?

No. Only candidates who have completed their degree are eligible.

3. Is there any employment bond or agreement?

No. There is no bond or service agreement required.

4. What is the salary offered?

The salary is ₹15,000 per month.

5. What type of experience will I gain in this role?

You will gain practical exposure to patient coordination, clinical data management, regulatory documentation, and ICH-GCP compliance within a clinical trial environment.

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Summary

Company	I’SHNOVA Clinical Trial Company
Vacancies	Junior Clinical Trial Coordinator
Required Education	B.Pharm, M.Pharm, MSc Life Sciences
Experience	Freshers Eligible

Tagged as: Pharma Jobs in Hyderabad