MDL CRC Hiring Freshers | Life Sciences | Multiple Cities
- Micro Data Labs Hiring Clinical Research Coordinators | Freshers Eligible | Multiple Locations
- Company Overview
- Job Role & Responsibilities
- Clinical Research Coordinator (CRC)
- Key Responsibilities
- Skills Gained in This Role
- Eligibility / Qualifications
- Educational Qualification
- Experience
- Required Skills
- Preferred Knowledge
- Location & Salary
- Location
- Salary
- Application Process
- Email ID
- Important Application Instruction
- Vacancies Available
- Important Note
- Frequently Asked Questions (FAQs)
- 1. Are freshers eligible for the Clinical Research Coordinator position?
- 2. Which qualifications are accepted for this role?
- 3. How many vacancies are available?
- 4. Is prior CRC experience mandatory?
- 5. What are the key responsibilities of a Clinical Research Coordinator?
- 6. How should candidates apply?
- Summary Table
Micro Data Labs Hiring Clinical Research Coordinators | Freshers Eligible | Multiple Locations
Candidates looking to build a career in clinical research have an excellent opportunity with Micro Data Labs (MDL). The organization is currently hiring Clinical Research Coordinators (CRC) for multiple locations across India. Freshers with a Life Sciences, Pharmacy, Nursing, or related healthcare background are encouraged to apply.
This recruitment drive is focused on immediate joiners who are passionate about clinical trials, patient coordination, clinical data management, and healthcare research. The role offers exposure to clinical trial operations, Good Clinical Practice (GCP) guidelines, regulatory compliance, and study coordination activities, making it an excellent entry point into the clinical research and CRO industry.
Company Overview
Micro Data Labs (MDL) is involved in supporting clinical research activities and healthcare data management services. The company works closely with investigators, sponsors, healthcare professionals, and research sites to ensure smooth execution of clinical studies while maintaining regulatory compliance and data quality standards.
Clinical Research Coordinators play a critical role in managing study activities, ensuring protocol adherence, maintaining trial documentation, and supporting communication between study participants and research teams. This position provides valuable experience for professionals interested in careers in Clinical Research, Clinical Operations, Pharmacovigilance, Data Management, Regulatory Affairs, and Clinical Trial Management.
As clinical research continues to expand globally, qualified CRC professionals remain in high demand across pharmaceutical companies, biotechnology organizations, CROs, hospitals, and research institutions.
Job Role & Responsibilities
Clinical Research Coordinator (CRC)
The selected candidates will be responsible for supporting the day-to-day management of clinical trials while ensuring compliance with study protocols, ethical guidelines, and regulatory requirements.
Key Responsibilities
- Ensure smooth execution of daily clinical trial activities.
- Collect, record, verify, and update clinical trial data accurately.
- Maintain study-related documentation and regulatory files.
- Prepare and share weekly study progress reports with clients and stakeholders.
- Handle data queries and coordinate timely resolution of discrepancies.
- Support monitoring visits, audits, and regulatory inspections.
- Coordinate with investigators, sponsors, and site staff for study-related activities.
- Conduct patient follow-ups to ensure protocol compliance and visit adherence.
- Maintain data integrity throughout the clinical study lifecycle.
- Ensure adherence to Good Clinical Practice (GCP) guidelines.
- Assist in study documentation, reporting, and trial management activities.
Skills Gained in This Role
- Clinical Trial Management
- Clinical Data Collection
- GCP Compliance
- Clinical Documentation
- Patient Coordination
- Audit Readiness
- Regulatory Compliance
- Clinical Operations
- Healthcare Data Management
- Research Site Coordination
These skills are highly valuable for professionals planning careers in CROs, pharmaceutical companies, hospitals, biotechnology firms, and healthcare consulting organizations.
Eligibility / Qualifications
Educational Qualification
Candidates must possess a Bachelor’s degree in any of the following disciplines:
- Life Sciences
- Pharmacy
- Nursing
- Biotechnology
- Microbiology
- Biochemistry
- Clinical Research
- Biomedical Sciences
- Allied Healthcare Sciences
- Healthcare Management
- Medical Laboratory Technology
Experience
- Freshers Eligible
- Prior Clinical Research Coordinator experience preferred
Required Skills
- Good communication skills
- Strong documentation abilities
- Organizational and multitasking skills
- Knowledge of clinical trial processes
- Understanding of GCP guidelines
- Awareness of regulatory requirements
- Ability to work independently
- Attention to detail and data accuracy
Preferred Knowledge
Candidates with exposure to the following areas may have an added advantage:
- Clinical Trial Operations
- Clinical Research Documentation
- ICH-GCP Guidelines
- Healthcare Compliance
- Patient Recruitment and Retention
- Clinical Data Management
- Research Site Activities
Location & Salary
Location
Kanpur, Hyderabad, Amritsar, Ludhiana
Salary
₹2.8 LPA – ₹4.5 LPA (Approximate)

Application Process
Interested candidates should send their updated resume to the official email address.
Email ID
Important Application Instruction
Candidates must use the following email subject line format:
CRC ; Location Name ; Experience
Example:
CRC ; Kanpur ; 6 Months Experience
Applications submitted without the prescribed subject format may not be shortlisted.
Vacancies Available
- Kanpur – 1 Position
- Hyderabad – 1 Position
- Amritsar – 1 Position
- Ludhiana – 1 Position
Important Note
Only candidates who can join immediately and reside near the respective job locations are encouraged to apply.
Frequently Asked Questions (FAQs)
1. Are freshers eligible for the Clinical Research Coordinator position?
Yes. Freshers with relevant educational qualifications can apply.
2. Which qualifications are accepted for this role?
Candidates from Life Sciences, Pharmacy, Nursing, Biotechnology, Clinical Research, and related healthcare disciplines are eligible.
3. How many vacancies are available?
There are four vacancies, with one opening each in Kanpur, Hyderabad, Amritsar, and Ludhiana.
4. Is prior CRC experience mandatory?
No. Prior experience is preferred but not mandatory. Freshers can also apply.
5. What are the key responsibilities of a Clinical Research Coordinator?
Responsibilities include clinical trial coordination, patient follow-up, clinical documentation, data collection, audit support, and regulatory compliance activities.
6. How should candidates apply?
Candidates must email their resume to careers@microdatalabs.com using the specified subject line format.
Summary Table
| Company | Micro Data Labs (MDL) |
|---|---|
| Department Vacancies | Clinical Research Coordinator (CRC) – 4 Vacancies |
| Qualification | Life Sciences, Pharmacy, Nursing, Biotechnology, Clinical Research, Allied Healthcare |
| Experience | Freshers Eligible / Experienced Preferred |
| Location | Kanpur, Hyderabad, Amritsar, Ludhiana |
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