The clinical research industry in India continues to witness remarkable growth as pharmaceutical companies and Contract Research Organizations (CROs) expand their research operations nationwide. This increasing demand has created exciting career opportunities for pharmacy professionals looking to build a successful career in clinical trials.

If you are a PharmD, B.Pharm, or M.Pharm graduate with 1–3 years of clinical research experience, here’s an excellent opportunity. Med Express Clinical Research Solutions Pvt. Ltd. (MECRS India) has announced Clinical Research Coordinator (CRC) vacancies at Chhatrapati Sambhajinagar (Aurangabad), Maharashtra.

This article covers the complete eligibility criteria, job responsibilities, preferred qualifications, and application process.

Job Highlights

Particular	Details
Company	Med Express Clinical Research Solutions Pvt. Ltd. (MECRS India)
Job Role	Clinical Research Coordinator (CRC)
Number of Vacancies	02
Location	Chhatrapati Sambhajinagar,Maharashtra
Qualification	PharmD / B.Pharm / M.Pharm
Experience	1–3 Years
Preferred Experience	Oncology Clinical Trials
Application Mode	Email
Email ID	hr@mecrsindia.com

About Med Express Clinical Research Solutions (MECRS India)

Med Express Clinical Research Solutions Pvt. Ltd. (MECRS India) is a leading Site Management Organization (SMO) that supports clinical trial operations across multiple therapeutic areas.

The organization works closely with:

Pharmaceutical companies
CROs
Hospitals
Principal Investigators

MECRS ensures clinical trials are conducted according to Good Clinical Practice (GCP) guidelines while maintaining high standards of patient safety, documentation, and regulatory compliance.

Working with an SMO provides excellent exposure to every stage of clinical trial management.

Clinical Research Coordinator (CRC) Responsibilities

Selected candidates will be responsible for coordinating day-to-day clinical trial activities.

Protocol Management

Understand study protocols thoroughly
Coordinate study visits
Ensure protocol compliance
Maintain study timelines

Patient Screening & Recruitment

Assist investigators in patient recruitment
Screen patients based on inclusion/exclusion criteria
Coordinate patient visits
Maintain participant records

Informed Consent Process

Explain study procedures
Ensure informed consent documentation
Maintain ethical standards
File signed consent documents

Clinical Documentation

Maintain essential clinical research documents including:

Investigator Site File (ISF)
Source Documents
Case Report Forms (CRFs)
Trial Master File (TMF)
Regulatory Documents

Laboratory & Investigational Product Management

Coordinate biological sample collection
Maintain sample shipment records
Monitor temperature logs
Handle Investigational Product (IP) accountability

Safety Reporting

Monitor Adverse Events (AE)
Report Serious Adverse Events (SAE)
Support investigators during safety reporting
Maintain regulatory compliance

Why Oncology Experience is Preferred

Candidates with Oncology Clinical Trial experience will have an added advantage because oncology studies involve:

Complex study protocols
Advanced treatment schedules
Intensive patient monitoring
Strict safety reporting
RECIST assessment knowledge
Long-term patient follow-up

Even candidates without oncology experience but possessing strong CRC knowledge and GCP understanding are encouraged to apply.

Eligibility Criteria

Applicants should possess one of the following qualifications:

PharmD
B.Pharm
M.Pharm

Experience Required

1–3 Years as Clinical Research Coordinator
Experience in clinical trial site operations
Knowledge of ICH-GCP Guidelines
Good documentation skills

Desired Skills

Candidates with the following skills will stand out:

GCP Knowledge
Clinical Documentation
Patient Coordination
Communication Skills
Regulatory Compliance
EDC System Exposure
Site Coordination
Time Management
Attention to Detail

Job Location

Chhatrapati Sambhajinagar (Aurangabad), Maharashtra

The city has become one of Maharashtra’s emerging pharmaceutical and healthcare hubs with growing opportunities in:

Clinical Research
Hospitals
Pharmaceutical Manufacturing
Biotechnology
Oncology Centers

How to Apply

Interested candidates should send their updated resume to:

Email: hr@mecrsindia.com

Recommended Email Subject

Application for Clinical Research Coordinator – Your Name – 2 Years Experience

Before applying, make sure your CV includes:

Therapeutic Areas Worked
Clinical Trial Experience
Audit Experience
GCP Training
EDC Experience
Current Organization
Notice Period

Why Join MECRS India?

Working as a Clinical Research Coordinator at MECRS offers:

Exposure to global clinical trials
Hands-on site management experience
Career growth in clinical research
Opportunity to work with experienced investigators
Strong learning environment
Exposure to oncology studies

Important Note

Only candidates meeting the required qualification and experience criteria are likely to be shortlisted. Candidates with prior oncology clinical trial experience will receive preference during the selection process.

Apply Now

Interested and eligible candidates can email their updated CV to:

📧 hr@mecrsindia.com

Apply as early as possible since only 02 vacancies are available.

Frequently Asked Questions (FAQs)

Is this job open for freshers?

No. Candidates should have 1–3 years of Clinical Research Coordinator experience.

Which qualifications are eligible?

PharmD
B.Pharm
M.Pharm

Is Oncology experience mandatory?

No, but it is highly preferred.

What is the job location?

Chhatrapati Sambhajinagar (Aurangabad), Maharashtra.

How can I apply?

Send your updated CV to hr@mecrsindia.com.

Med Express Clinical Hiring 2026: Urgent Vacancies for Clinical Research Coordinators (CRC) in Chh. Sambhajinagar