HBCHRC Visakhapatnam Trial Coordinator Recruitment 2026: Walk-in Interview for Trial Coordinator Post
The Homi Bhabha Cancer Hospital and Research Centre (HBCHRC), Visakhapatnam has invited eligible candidates to attend a Walk-in Interview for the post of Trial Coordinator. This recruitment offers an excellent opportunity for candidates interested in clinical research, healthcare project management, clinical trials, patient coordination, and medical research administration.
The Trial Coordinator position is ideal for individuals who want to work in a professional healthcare research environment and contribute to medical advancements through scientific studies and clinical research programs. Selected candidates will assist research teams, coordinate trial activities, manage documentation, and support clinical research projects.
For candidates seeking a career in clinical research, pharmaceutical studies, healthcare management, and medical project coordination, this recruitment provides valuable professional exposure.
About Homi Bhabha Cancer Hospital and Research Centre (HBCHRC)
Homi Bhabha Cancer Hospital and Research Centre (HBCHRC) is a premier cancer treatment and research institution dedicated to providing advanced oncology care, medical research, and healthcare education.
The institution is known for:
- Cancer Treatment Services
- Clinical Research Programs
- Oncology Studies
- Medical Education
- Translational Research
- Public Health Initiatives
- Healthcare Innovation
- Patient-Centered Care
HBCHRC regularly conducts clinical trials and research studies aimed at improving treatment methods and healthcare outcomes.
HBCHRC Visakhapatnam Recruitment 2026 Overview
Organization Name: Homi Bhabha Cancer Hospital and Research Centre (HBCHRC), Visakhapatnam
Post Name: Trial Coordinator
Recruitment Mode: Walk-in Interview
Application Mode: Walk-in
Job Location: Visakhapatnam, Andhra Pradesh
Job Category: Clinical Research Jobs
Employment Type: Contractual
Selection Process: Walk-in Interview and Document Verification
About the Trial Coordinator Position
The Trial Coordinator acts as a bridge between investigators, patients, sponsors, healthcare professionals, and research teams.
The role involves:
- Clinical Trial Coordination
- Patient Follow-up
- Study Documentation
- Research Data Management
- Regulatory Compliance
- Trial Monitoring
- Research Administration
The position offers practical exposure to healthcare research and clinical trial operations.
Educational Qualification
Candidates should possess qualifications relevant to healthcare and research fields.
Preferred Qualifications
Applicants may possess:
- B.Sc Nursing
- B.Pharm
- Pharm.D
- Life Sciences Degree
- Biotechnology Degree
- Clinical Research Qualification
- Medical Laboratory Technology Qualification
- Master’s Degree in Relevant Discipline
Candidates with certifications in clinical research or healthcare management may receive preference.
Experience Requirement
Relevant experience in clinical research and healthcare projects can be advantageous.
Preferred Experience Areas
- Clinical Trials
- Research Coordination
- Patient Management
- Clinical Data Management
- Hospital Administration
- Pharmaceutical Research
- Oncology Research
- Healthcare Documentation
- Regulatory Compliance
Fresh candidates with strong academic credentials may also be considered depending on recruitment requirements.
Age Limit
Candidates should satisfy the age criteria prescribed by the institution.
Minimum Age
As per recruitment norms.
Maximum Age
According to institutional guidelines.
Age Relaxation
Applicable for eligible categories as per government and institutional rules.
Salary Structure
Selected candidates will receive remuneration according to institutional and project guidelines.
Benefits
- Attractive Monthly Salary
- Clinical Research Experience
- Exposure to Oncology Research
- Professional Development Opportunities
- Healthcare Industry Experience
- Career Advancement Opportunities
The position offers significant learning opportunities in the clinical research sector.
Roles and Responsibilities
Clinical Trial Coordination
Selected candidates may be responsible for:
- Coordinating research activities.
- Supporting principal investigators.
- Managing study schedules.
- Ensuring protocol compliance.
Patient Coordination
Responsibilities may include:
- Scheduling patient visits.
- Conducting follow-up activities.
- Coordinating appointments.
- Maintaining participant records.
Documentation Management
Trial Coordinators are expected to:
- Maintain study files.
- Update trial records.
- Prepare project reports.
- Manage research documentation.
Data Collection and Reporting
Responsibilities may include:
- Collecting clinical data.
- Recording study observations.
- Supporting database management.
- Assisting data verification activities.
Regulatory Compliance
Selected candidates may assist in:
- Maintaining ethical standards.
- Supporting audit processes.
- Ensuring study compliance.
- Preparing regulatory documents.
Why Join HBCHRC Visakhapatnam?
Prestigious Healthcare Institution
HBCHRC is recognized for excellence in cancer treatment and medical research.
Research Exposure
Candidates gain practical experience in clinical trials and healthcare projects.
Career Development
The position helps build expertise in clinical research and project coordination.
Professional Learning
Exposure to advanced healthcare systems and multidisciplinary teams.
Networking Opportunities
Interaction with doctors, researchers, scientists, and healthcare professionals.
Future Career Growth
Clinical trial experience is highly valued in:
- Pharmaceutical Companies
- Research Organizations
- Hospitals
- Biotechnology Firms
- Clinical Research Institutions
Selection Process
The recruitment process generally includes:
Walk-in Interview
Eligible candidates must attend the walk-in interview.
The interview may assess:
- Clinical Research Knowledge
- Healthcare Awareness
- Documentation Skills
- Communication Ability
- Professional Competence
Document Verification
Candidates must produce original documents.
Documents may include:
- Educational Certificates
- Clinical Research Certifications
- Experience Certificates
- Identity Proof
- Passport-size Photographs
Final Selection
Selection may be based on:
- Educational Qualifications
- Professional Experience
- Interview Performance
- Document Verification
Skills Required
Successful candidates should possess:
Clinical Research Knowledge
Understanding of research processes and trial management.
Communication Skills
Ability to interact effectively with patients and healthcare professionals.
Documentation Skills
Accurate maintenance of records and reports.
Organizational Ability
Capability to coordinate multiple research activities.
Analytical Skills
Ability to review and interpret research information.
Teamwork
Capability to collaborate with multidisciplinary research teams.
Documents Required
Candidates should carry the following documents.
Educational Documents
- Degree Certificates
- Mark Sheets
- Clinical Research Certifications
Professional Documents
- Experience Certificates
- Internship Certificates
- Training Records
Personal Documents
- Aadhaar Card
- PAN Card
- Passport-size Photographs
Additional Documents
- Updated Resume
- Identity Proof
- Category Certificate (if applicable)
How to Attend the Walk-in Interview
Step 1
Read the recruitment notification carefully.
Step 2
Verify eligibility requirements.
Step 3
Arrange all educational and professional documents.
Step 4
Prepare an updated resume.
Step 5
Reach the interview venue before the reporting time.
Step 6
Complete registration and verification formalities.
Step 7
Attend the interview before the selection committee.
Step 8
Await the final selection results.
Career Opportunities After Selection
Experience as a Trial Coordinator can lead to opportunities in:
Clinical Research Sector
- Clinical Research Associate
- Clinical Trial Coordinator
- Clinical Project Manager
- Regulatory Affairs Executive
Healthcare Industry
- Hospital Research Departments
- Pharmaceutical Companies
- Biotechnology Organizations
- Medical Research Institutes
Research and Development
- Research Associate
- Project Coordinator
- Clinical Data Specialist
- Healthcare Research Professional
The experience gained at a reputed institution like HBCHRC significantly strengthens future career prospects.
Frequently Asked Questions (FAQs)
What is the post announced under HBCHRC Visakhapatnam Recruitment 2026?
The recruitment is for the post of Trial Coordinator.
What is the mode of recruitment?
Selection will be conducted through a Walk-in Interview.
What qualification is required?
Candidates may possess qualifications such as:
- B.Sc Nursing
- B.Pharm
- Pharm.D
- Life Sciences Degree
- Biotechnology Degree
- Clinical Research Qualification
What is the selection process?
Selection generally includes:
- Walk-in Interview
- Document Verification
Is clinical research experience required?
Relevant experience is preferred, but eligibility depends on recruitment requirements.
Why should candidates apply?
The recruitment offers research exposure, healthcare experience, professional development opportunities, and career growth in the clinical research field.
Is this suitable for healthcare graduates?
Yes. The position provides valuable experience in clinical trials, patient coordination, research administration, and healthcare project management.
Important Links
Official Notification: Click Here
The HBCHRC Visakhapatnam Trial Coordinator Recruitment 2026 is an excellent opportunity for candidates interested in clinical research, oncology studies, and healthcare project management. The position offers exposure to advanced medical research, patient-focused healthcare services, and multidisciplinary research teams, making it an ideal platform for building a successful career in the clinical research and healthcare industry.
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