Selected candidates will work closely with Principal Investigators, sponsors, ethics committees, and study teams to ensure clinical studies are conducted efficiently while maintaining regulatory compliance and participant safety.
Job Overview
| Particulars | Details |
|---|---|
| Position | Clinical Research Coordinator |
| Company | PFC Pharna |
| Location | Hyderabad, Bengaluru |
| Job Type | Full-Time |
| Experience | Fresher |
| Category / Department | CDM |
| Application Mode | Online |
💡 Editor's Note / Preparation Tip
Clinical Research Coordinators play a vital role in ensuring that clinical trials are conducted ethically, safely, and in compliance with regulatory standards. This opportunity at PFC Pharma Focus offers professionals the chance to strengthen their expertise in patient coordination, study management, regulatory documentation, and Good Clinical Practice while contributing to high-quality clinical research. Candidates with prior CRC experience who are looking to expand their careers in clinical operations and site management may find this role particularly rewarding.
📝 Job Description
🚀 PFC Pharma Focus Hiring for Clinical Research Coordinators | Hyderabad, Bengaluru & Bhubaneswar | 1–2 Years
Clinical Research Coordinator
PFC Pharma Focus
Qualification: B.Pharm, M.Pharm, BDS, MDS, BAMS, BHMS, PG Diploma, or other relevant Life Sciences specializations
Experience: 1–2 Years
Job Locations: Hyderabad (Banjara Hills), Bhubaneswar
Employment Type: Full-Time | Permanent
Industry: Pharmaceutical & Life Sciences
Department: Clinical Research / Research & Development
Application Mode: Online
🎓 Eligibility Criteria
Applicants should possess:
• B.Pharm in Clinical Pharmacy, Pharmacology, or related specialization.
• M.Pharm candidates are also eligible.
• Other relevant qualifications such as BDS, MDS, BAMS, BHMS, PG Diploma, or related Life Sciences specializations may also apply.
• 1–2 years of Clinical Research Coordinator experience.
• Good understanding of clinical research processes and regulatory requirements.
📍 Job Locations
• Hyderabad – Banjara Hills
• Bengaluru – Bommasandra
• Bhubaneswar – Nayapalli
Candidates willing to work at any of the above locations are encouraged to apply.
🌟 Why Join PFC Pharma Focus?
• Opportunity to work on global clinical research projects.
• Hands-on experience in clinical operations and site management.
• Exposure to regulatory documentation and GCP compliance.
• Work alongside experienced investigators and sponsor teams.
• Excellent learning environment for career growth in clinical research.
• Gain expertise in patient management, trial coordination, and clinical operations.
📢 Stay updated with the latest opportunities in Clinical Research, Pharmacovigilance, Medical Writing, Regulatory Affairs, SAS Programming, Biotechnology, and the Pharmaceutical Industry through
🎯 Key Responsibilities
- ✓ As a Clinical Research Coordinator, you will:
- ✓ Coordinate study start-up activities within project timelines.
- ✓ Prepare and maintain essential clinical trial documentation.
- ✓ Ensure study sites are ready before Site Initiation Visits (SIV).
- ✓ Coordinate Ethics Committee submissions and regulatory approvals.
- ✓ Assist investigators with patient pre-screening and recruitment.
- ✓ Support patient enrollment and retention throughout the study.
- ✓ Conduct protocol-specific patient visit activities.
- ✓ Perform electronic data entry and resolve data queries.
- ✓ Coordinate sponsor monitoring visits and site audits.
- ✓ Maintain accurate study records and documentation.
- ✓ Ensure compliance with study protocols, ICH-GCP guidelines, and applicable regulations.
- ✓ Support adverse event documentation and safety reporting.
💡 Required Qualifications & Skills
🚀 Career Guidance & Interview Insights
To help you succeed, we've compiled original preparation guides, resume keywords, and growth analytics for this category of role.
This Clinical Research Coordinator role is a chance to contribute directly to life sciences, patient care, or pharmaceutical advancements. You will work within strict compliance frameworks, ensure rigorous quality standards, and collaborate with technical or medical experts. It is a career path that blends scientific excellence with a deep sense of social purpose.
Healthcare and pharmaceutical professionals grow through specialized scientific experience. Entry-level starts as Lab Technician, Chemist, or Quality Associate, progressing to Senior QA/QC Analyst. Advancement leads to Lab Supervisor, Clinical Project Manager, and senior management roles like Quality Director, VP of Regulatory Affairs, or Chief Scientific Officer.
Expected Technical & Behavioral Questions:
- Q1: How do you ensure compliance with WHO/GMP guidelines during laboratory operations?
Answer Tip: Mention strict adherence to Standard Operating Procedures (SOPs), detailed batch records, regular equipment calibration, and sanitization cycles. - Q2: What steps do you take when a quality deviation is detected in a product batch?
Answer Tip: Outline immediate isolation of the batch, raising a deviation report, root cause analysis (RCA), and initiating CAPA (Corrective and Preventive Action). - Q3: How do you manage safety protocols while handling toxic chemicals?
Answer Tip: Discuss using Material Safety Data Sheets (MSDS), wearing appropriate Personal Protective Equipment (PPE), proper ventilation, and chemical spill kits.
To pass automated ATS (Applicant Tracking System) screening and catch the recruiter's eye, tailor your resume with the following tips:
- Keywords to include: Quality Control (QC), GMP Compliance, FDA Regulations, SOP Documentation, HPLC/GC analysis, Batch Validation, Clinical Trials, Pharmacovigilance.
- Format: List laboratory skills and instruments handled (e.g. HPLC, spectrophotometer) in a dedicated technical matrix.
- Quantify Results: E.g., 'Validated 15 batch formulations under GMP guidelines with zero quality defects.'
Estimated compensation for this role type in India is ₹2,40,000 - ₹3,80,000 per annum (Fresher analyst). The actual salary package offered depends on factors such as company size, work mode (remote or on-site), individual technical proficiency, and negotiations during final HR rounds.
Key credentials: GMP Certified Professional (ASQ), Certified Clinical Research Coordinator (CCRC), or specialized laboratory training certificates in high-performance liquid chromatography (HPLC) and safety standards.
Frequently Asked Questions
1. What is the job role being offered?
The position is for Clinical Research Coordinator (CRC).
2. Which locations have openings?
Openings are available in Hyderabad, Bengaluru, and Bhubaneswar.
3. What experience is required?
Candidates should have 1–2 years of Clinical Research Coordinator experience.
4. Which qualifications are eligible?
B.Pharm, M.Pharm, BDS, MDS, BAMS, BHMS, PG Diploma, and other relevant Life Sciences qualifications.
5. Is this a permanent position?
Yes. It is a full-time permanent opportunity.
6. What are the major responsibilities of a Clinical Research Coordinator?
Responsibilities include study coordination, patient recruitment, regulatory documentation, ethics submissions, site management, data entry, sponsor coordination, and maintaining GCP compliance.
7. Is knowledge of GCP important for this role?
Yes. A good understanding of Good Clinical Practice (GCP) and clinical research regulations is highly preferred.
8. Will candidates interact with investigators and sponsors?
Yes. The role involves close coordination with Principal Investigators, sponsors, ethics committees, and clinical trial teams.
9. What skills can help candidates succeed in this position?
Clinical trial coordination, patient management, EDC systems, documentation, communication skills, regulatory compliance, and teamwork.
10. Why should candidates consider this opportunity?
This role offers valuable exposure to global clinical trials, strengthens clinical operations experience, and provides long-term career growth in the clinical research industry.
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