This opportunity is designed for fresh graduates seeking structured entry into clinical research operations within the pharmaceutical industry.
The role is based in Mumbai, with work locations at Malad and Dadar.
It matters because it provides hands-on exposure to regulated clinical trial coordination at the site and sponsor interface level.
About the Company
Meyer Organics Private Limited is an Indian pharmaceutical company engaged in the development, manufacturing, and marketing of branded formulations across multiple therapeutic segments.
The organization operates with a strong focus on compliance, documentation accuracy, and ethical clinical practices.
Meyer Organics supports clinical and medical services functions that align with national and international regulatory expectations.
Job Overview
- Job Title: Clinical Research Coordinator (CRC)
- Company: Meyer Organics Private Limited
- Employment Type: Contractual (6 months)
- Experience Level: Freshers
- Monthly Salary: ₹20,000
- Location: Malad / Dadar, Mumbai
- Application Deadline: 15 January 2025
Key Responsibilities
Core Responsibilities
Clinical Research Coordinators at Meyer Organics support the day-to-day execution of clinical research activities in alignment with approved study protocols.
The role involves close coordination with investigators, clinical teams, and internal medical services.
Accuracy, documentation discipline, and adherence to regulatory guidelines are central to this position.
Key responsibilities include:
- Assisting in the coordination of clinical trials at study sites
- Supporting investigators in protocol adherence and study procedures
- Maintaining essential trial documents and study files
- Ensuring timely and accurate data collection from clinical sites
- Supporting subject enrollment and visit scheduling activities
Area-Specific Responsibilities
Given the coordinator-focused nature of the role, emphasis is placed on operational and documentation activities.
Candidates will contribute to compliance monitoring and internal reporting processes.
Additional responsibilities include:
- Supporting informed consent documentation processes
- Assisting in adverse event documentation and follow-up
- Coordinating communication between sites and internal teams
- Supporting audit and inspection readiness activities
- Ensuring compliance with GCP and internal SOPs
Eligibility & Skills
Educational Eligibility
Candidates must hold one of the following qualifications:
- D.Pharm
- B.Pharm
- M.Pharm
- B.Sc in Life Sciences
- M.Sc in Life Sciences
Fresh graduates and recent pass-outs are eligible to apply.
Required Skills
Only role-relevant skills are expected at entry level.
The position focuses on foundational clinical research competencies rather than advanced specialization.
Essential skills include:
- Basic understanding of clinical research and trial processes
- Familiarity with Good Clinical Practice (GCP) principles
- Strong documentation and record-keeping ability
- Attention to detail and data accuracy
- Clear written and verbal communication skills
- Ability to follow standard operating procedures
Why This Role Matters
Clinical Research Coordinators play a critical role in ensuring that clinical trials are conducted ethically, accurately, and in compliance with regulatory standards.
For freshers, this position provides early exposure to the operational backbone of clinical research.
It bridges academic knowledge with real-world application by involving candidates in live study coordination.
The role builds a strong foundation in clinical documentation, protocol adherence, and site coordination, which are essential competencies across clinical research, pharmacovigilance, and regulatory functions.
Benefits & Exposure
Although contractual, the role offers meaningful professional exposure within a regulated pharmaceutical environment.
Candidates gain direct experience in clinical trial coordination rather than observational or theoretical assignments.
Key benefits include:
- Practical exposure to active clinical research operations
- Hands-on involvement in clinical documentation workflows
- Experience working with investigators and medical teams
- Understanding of regulatory and compliance-driven processes
- Structured entry into the clinical research domain
Career Path After This Role
Experience as a Clinical Research Coordinator creates multiple progression pathways within the life sciences industry.
After completing this role, candidates may pursue positions based on performance and interest.
Potential next roles include:
- Senior Clinical Research Coordinator
- Clinical Trial Assistant (CTA)
- Clinical Research Associate (CRA – with additional training)
- Pharmacovigilance Executive
- Clinical Data Coordinator
- Regulatory Affairs or Medical Affairs support roles
This role is particularly valuable for candidates planning long-term careers in clinical research and drug development.
How to Apply
Eligible and interested candidates should submit their updated CV via email.
Ensure that educational qualifications and contact details are clearly mentioned in the resume.
Application Email:
Career@meyer.co.in
Application Deadline:
15 January 2025
Only shortlisted candidates may be contacted for further steps.
