Clinical Research Coordinator: The clinical research industry is rapidly expanding, creating exciting opportunities for life science and pharmacy graduates. One such highly sought-after role is that of a Clinical Research Coordinator (CRC)—a critical position responsible for managing and executing clinical trials at the site level.
Recently, Ethyra Global Research Solutions announced openings for the position of Clinical Research Coordinator (CRC) across multiple locations in India, including Amravati, Indore, Jabalpur, and Bhopal. This opportunity is particularly valuable for both freshers and experienced professionals aiming to build or advance their careers in clinical research.
In this blog, we’ll explore everything you need to know about this opportunity, the CRC role, required skills, career growth, and how you can apply successfully.
What is a Clinical Research Coordinator (CRC)?
A Clinical Research Coordinator (CRC) plays a pivotal role in the successful execution of clinical trials. They act as a bridge between investigators, sponsors, patients, and regulatory authorities.
Company: Ethyra Global Research Solutions
Locations: Amravati | Indore | Jabalpur | Bhopal
Role: Clinical Research Coordinator (CRC)
CRCs ensure that clinical studies are conducted in compliance with ICH-GCP (International Council for Harmonisation – Good Clinical Practice) guidelines, regulatory requirements, and study protocols.
About the Hiring Organization
Ethyra Global Research Solutions is actively seeking detail-oriented and motivated individuals to support site-level clinical trial operations. The organization focuses on maintaining high standards in research quality, compliance, and patient safety.
Key Responsibilities of a Clinical Research Coordinator
The CRC role is dynamic and involves a wide range of responsibilities. Let’s break them down in detail:
1. Trial Coordination & Site Management
- Oversee daily clinical trial activities at the site
- Coordinate with investigators, sponsors, and CROs
- Ensure timely execution of study protocols
- Manage study timelines and milestones
2. Informed Consent & Patient Recruitment
- Explain study protocols to potential participants
- Obtain Informed Consent Forms (ICF) ethically and legally
- Screen and recruit eligible patients
- Maintain patient confidentiality and safety
3. Documentation & Data Management
- Maintain accurate source documents
- Complete Case Report Forms (CRFs)
- Manage Site Master File (SMF) documentation
- Ensure data integrity and accuracy
4. Compliance with ICH-GCP Guidelines
- Ensure adherence to regulatory standards
- Follow ethical guidelines in clinical research
- Prepare for inspections and audits
5. Monitoring Visits & Audit Support
- Assist during sponsor monitoring visits
- Facilitate audits and inspections
- Address queries raised by monitors
- Ensure corrective and preventive actions (CAPA)
Eligibility Criteria for CRC Position
This opportunity is open to candidates from diverse educational backgrounds in life sciences and pharmacy:
Educational Qualifications:
- B.Sc (Life Sciences)
- M.Sc
- B.Pharm
- M.Pharm
- Pharm.D
Experience:
- Freshers are welcome
- Experienced professionals can also apply
Preferred Skills:
- Basic knowledge of GCP guidelines
- Understanding of clinical trial processes
- Good communication and organizational skills
- Attention to detail
Job Locations
The available positions are spread across key cities in Madhya Pradesh and Maharashtra:
- Amravati
- Indore
- Jabalpur
- Bhopal
This provides flexibility for candidates seeking opportunities in central India.
Why Choose a Career as a Clinical Research Coordinator?
A CRC role is one of the best entry points into the clinical research industry. Here’s why:
1. High Demand Industry
Clinical research is growing globally, increasing demand for skilled professionals.
2. Strong Career Growth
- CRC → Senior CRC
- Clinical Research Associate (CRA)
- Clinical Trial Manager (CTM)
3. Hands-On Experience
You gain direct exposure to:
- Patient interaction
- Regulatory compliance
- Real-world clinical trials
4. Global Opportunities
Experience in CRC roles opens doors to international clinical research careers.
Skills That Will Give You an Edge
To stand out as a CRC candidate, focus on developing:
- Knowledge of ICH-GCP guidelines
- Clinical trial documentation skills
- Communication and interpersonal abilities
- Time management and multitasking
- Problem-solving mindset
How to Apply for the CRC Position
Interested candidates can apply directly via email:
📧 [email protected]
Tips for Application:
- Create a professional CV highlighting clinical knowledge
- Mention any certifications (GCP, Pharmacovigilance, Clinical Research)
- Add internships or project experience
- Write a concise and impactful cover letter
