Curaclin Research Freshers Hiring Clinical Research Coordinator Jobs in Bhubaneswar. Freshers can start careers in clinical trials management today.
Introduction
Curaclin Research has announced an excellent career opportunity for aspiring clinical research professionals by opening applications for the position of Clinical Research Coordinator (CRC) in Bhubaneswar, Odisha. This opportunity is ideal for B.Pharm, M.Pharm, and Life Sciences graduates who are looking to establish a successful career in clinical research, trial management, and regulatory compliance. Freshers with strong academic knowledge of clinical research processes and ICH-GCP guidelines are encouraged to apply. As one of the promising Pharma Jobs 2026, this position provides hands-on exposure to clinical trial coordination, regulatory documentation, patient management, and sponsor communication within a professional clinical research environment.
About Company
Curaclin Research is a clinical research and site management organization (SMO) dedicated to supporting high-quality clinical trials across various therapeutic areas. The organization works closely with investigators, sponsors, contract research organizations (CROs), and healthcare institutions to ensure the efficient execution of clinical studies while maintaining compliance with international regulatory standards.
With a strong focus on ethical research practices and patient safety, Curaclin Research provides comprehensive clinical trial management services including site coordination, regulatory support, patient recruitment, documentation management, and quality assurance. The organization follows International Council for Harmonisation Good Clinical Practice (ICH-GCP) guidelines and supports studies that contribute to the advancement of healthcare and medical science.
By offering practical training and exposure to real-world clinical trial operations, Curaclin Research serves as an excellent platform for pharmacy and life sciences professionals seeking long-term careers in clinical research and drug development.
About Pharmajobhub.in
Pharmajobhub.in is a leading platform for pharmaceutical, biotechnology, healthcare, clinical research, and life sciences career opportunities across India. The website regularly shares latest pharma jobs, B.Pharm jobs, M.Pharm jobs, pharmacovigilance jobs, regulatory affairs openings, production vacancies, quality assurance careers, clinical research jobs, and freshers pharma jobs from reputed pharmaceutical companies nationwide.
Job Details / Job Summary
| Particulars | Details |
|---|---|
| Company Name | Curaclin Research |
| Job Role | Clinical Research Coordinator (CRC) |
| Department | Clinical Research |
| Qualification Required | B.Pharm, M.Pharm, Life Sciences |
| Experience Required | Freshers Eligible |
| Salary Package | ₹2.8 LPA – ₹5.5 LPA (Expected) |
| Job Location | Bhubaneswar, Odisha |
| Employment Type | Full-Time |
| Industry Type | Clinical Research / Site Management Organization (SMO) |
| Shift Timing | General Shift |
| Gender Eligibility | Male & Female |
| Application Mode | Email Application |
| Selection Process | Resume Screening, Technical Interview, HR Discussion |
| Skills Required | Clinical Research, ICH-GCP, Documentation, Site Coordination, Patient Management |
| Official Notification Status | Active |
| Application Last Date | Apply As Soon As Possible |
Eligibility Criteria
Candidates applying for this Pharma Company Hiring opportunity should meet the following requirements:
- B.Pharm degree from a recognized institution.
- M.Pharm degree from a recognized university.
- Bachelor’s or Master’s degree in Life Sciences.
- Basic understanding of clinical trial processes.
- Knowledge of ICH-GCP guidelines and research ethics.
- Good communication and documentation skills.
- Ability to coordinate with multiple stakeholders.
- Freshers are eligible to apply.
- Prior clinical research or site management exposure will be an added advantage.
Required Skills
The ideal candidate should possess the following professional skills:
- Clinical trial coordination.
- Understanding of ICH-GCP guidelines.
- Regulatory documentation management.
- Investigator Site File (ISF) maintenance.
- Patient screening and recruitment support.
- Clinical data entry and query management.
- Audit and inspection readiness.
- Communication with Sponsors and CROs.
- Time management and organizational skills.
- Attention to detail and compliance awareness.
- Medical and scientific documentation skills.
- Problem-solving and analytical thinking.
These skills are highly valuable for professionals pursuing Clinical Research Jobs, Pharmacovigilance Jobs, Regulatory Affairs Jobs, Drug Safety Careers, and other healthcare research opportunities.
Roles and Responsibilities
Selected candidates will be responsible for supporting and coordinating clinical trial activities at the study site.
- Coordinate day-to-day clinical trial activities according to approved study protocols.
- Assist the Principal Investigator (PI) in study conduct and management.
- Support patient screening, enrollment, recruitment, and follow-up visits.
- Maintain Investigator Site Files (ISF) and regulatory documentation.
- Ensure compliance with ICH-GCP guidelines and regulatory requirements.
- Assist in clinical trial data entry and query resolution activities.
- Coordinate communication between sponsors, CROs, investigators, and study staff.
- Prepare and maintain essential trial documents.
- Support monitoring visits conducted by sponsors and CRO representatives.
- Assist during audits, inspections, and compliance reviews.
- Track study timelines and participant visits.
- Maintain confidentiality of patient and study-related information.
- Ensure protocol adherence throughout the study lifecycle.
- Support site readiness and documentation quality initiatives.
Salary Details
Curaclin Research offers competitive compensation packages depending on educational qualifications, skill level, and interview performance.
Expected Salary Range: ₹2.8 Lakhs to ₹5.5 Lakhs per annum
Additional Benefits
- Exposure to real-time clinical trial operations.
- Hands-on experience in site management.
- Training in regulatory documentation and compliance.
- Interaction with Sponsors, CROs, and Investigators.
- Professional development opportunities.
- Strong career pathway toward CRA and Site Management roles.
- Learning opportunities within the clinical research industry.
Selection Process
The hiring process generally consists of the following stages:
Step 1: Application Submission
Interested candidates must submit their updated resumes through the official email addresses.
Step 2: Resume Screening
The recruitment team reviews applications based on educational qualifications and suitability for the CRC role.
Step 3: Technical Evaluation
Shortlisted candidates may be assessed on clinical research concepts, ICH-GCP knowledge, and documentation practices.
Step 4: Personal Interview
Candidates interact with hiring managers and research professionals to evaluate communication skills and professional aptitude.
Step 5: HR Discussion
Compensation, joining timelines, and employment conditions are discussed.
Step 6: Final Selection
Selected candidates receive official communication regarding onboarding and joining formalities.
How to Apply
Interested and eligible candidates can apply by sending their updated resume to the following email addresses:
Email ID 1: hr.curaclinresearch@gmail.com
Email ID 2: bd@curaclinsmo.com
Application Guidelines
- Mention “Application for Clinical Research Coordinator” in the email subject line.
- Attach an updated resume in PDF format.
- Highlight clinical research projects, internships, or relevant coursework.
- Include educational qualifications and contact information.
- Mention current location and availability for joining.
Candidates are encouraged to apply at the earliest as applications may be reviewed continuously until suitable candidates are selected.
Frequently Asked Questions (FAQs)
1. What qualifications are required for the Clinical Research Coordinator position?
Candidates must possess B.Pharm, M.Pharm, or Life Sciences qualifications from a recognized institution or university.
2. Are freshers eligible to apply for this CRC job?
Yes, freshers with knowledge of clinical research processes and ICH-GCP guidelines are eligible to apply.
3. What salary can candidates expect at Curaclin Research?
The estimated salary package ranges between ₹2.8 LPA and ₹5.5 LPA depending on qualifications, skills, and interview performance.
4. How can I apply for the Curaclin Research Clinical Research Coordinator vacancy?
Interested candidates can submit their updated resume through the official recruitment email addresses provided in the notification.
