Clinical Research Data Coordinator Job: Are you looking to start or grow your career in clinical research, healthcare data management, oncology research, or clinical trials? An excellent opportunity is now open for the position of Clinical Research Data Coordinator in the specialized Hemato-Oncology Department at a reputed cancer research and treatment center based in Delhi NCR.
This role is ideal for candidates who are passionate about working in the healthcare, pharmaceutical, and clinical research industries, and who want to build a strong foundation in clinical data handling, research coordination, and regulatory-compliant processes. If you have a background in life sciences, biotechnology, pharmacy, or related disciplines, and are eager to gain practical exposure in real-world clinical research environments, this position can be a valuable step forward in your professional journey.
Job Location
Rohini Sector 5, New Delhi, India
Located in a well-established healthcare zone, this role offers exposure to a multidisciplinary clinical environment, advanced medical infrastructure, and collaborative research teams focused on improving cancer treatment outcomes.
Experience Requirement
- Minimum Experience: 6 months
- Maximum Experience: 12 months
Candidates with prior experience or internships in clinical research, hospital data management, pharmacovigilance, clinical trials, or healthcare analytics will be given preference. Freshers with strong theoretical knowledge and a willingness to learn may also be considered.
Comprehensive Job Description of Clinical Research Data Coordinator Job
The Clinical Research Data Coordinator plays a vital role in ensuring the accuracy, reliability, and completeness of clinical research data. This position involves working closely with principal investigators, oncologists, research scientists, clinical staff, and study coordinators to support ongoing and upcoming clinical trials.
You will be responsible for managing large volumes of patient-related data, study documentation, and research records, ensuring that all information is captured and maintained according to clinical protocols, ethical standards, and regulatory requirements.
This role requires a high level of precision, consistency, confidentiality, and coordination, making it an excellent opportunity for individuals who are detail-oriented and interested in contributing to evidence-based medicine and life-saving research.
Detailed Roles and Responsibilities
- Perform accurate and timely collection, entry, and validation of clinical research data
- Maintain and manage case report forms (CRFs), electronic databases, and study documentation
- Coordinate with investigators, doctors, nurses, and research teams for data clarification and updates
- Conduct regular data quality checks, audits, and verification processes to ensure accuracy
- Ensure compliance with clinical trial protocols, ICH-GCP guidelines, and regulatory frameworks
- Assist in preparing and organizing study-related reports, files, and documentation
- Track patient progress, study milestones, and research timelines
- Identify discrepancies or missing data and resolve them through proper communication channels
- Maintain strict confidentiality and security of patient and research data
- Support ongoing clinical trials and contribute to the smooth execution of research activities
- Assist in audit preparation and documentation review for regulatory inspections
Educational Qualifications and Eligibility
- Bachelor’s or Master’s degree in:
- Life Sciences
- Biotechnology
- Pharmacy
- Microbiology
- Biochemistry
- Or any related healthcare or biomedical field
- Basic understanding of:
- Clinical research processes
- Clinical trial phases
- Data collection and documentation standards
- Strong attention to detail and accuracy in handling data
- Good communication and coordination skills
- Ability to work independently as well as in a team environment
Preferred Skills and Technical Competencies
- Knowledge of Good Clinical Practice (GCP) and regulatory guidelines
- Familiarity with clinical trial documentation and protocols
- Basic experience with Electronic Data Capture (EDC) systems
- Proficiency in Microsoft Excel, Word, and data management tools
- Analytical mindset with problem-solving capabilities
- Ability to manage multiple tasks and meet deadlines efficiently
- Strong organizational and documentation skills
Career Scope and Growth Opportunities
This role offers significant opportunities for long-term career growth in the clinical research and healthcare industries. With experience, candidates can progress into roles such as:
- Clinical Research Associate (CRA)
- Clinical Data Manager
- Clinical Trial Coordinator
- Pharmacovigilance Associate
- Regulatory Affairs Executive
- Medical Data Analyst
The experience gained in this role will help you build expertise in clinical trial operations, regulatory compliance, and healthcare data systems, which are highly valued skills in both national and international pharmaceutical and research organizations.
Work Environment and Learning Exposure
- Work in a high-impact oncology research setting
- Gain exposure to real-time clinical trials and patient data management
- Collaborate with experienced oncologists, researchers, and healthcare professionals
- Learn industry-standard practices in clinical documentation and regulatory compliance
- Be part of a team contributing to advancements in cancer research and treatment
Application Process
Interested candidates who meet the above criteria are encouraged to apply by sending their updated resume/CV to:
While applying, ensure that your CV highlights:
- Relevant academic background
- Any clinical research or healthcare-related experience
- Technical skills related to data handling or research
Why You Should Apply
- Start your career in the fast-growing clinical research and healthcare sector
- Gain practical experience in clinical trials and oncology research
- Work in a reputed medical and research environment
- Contribute to life-saving innovations and patient care advancements
- Build a strong foundation for a long-term career in pharma, biotech, and healthcare industries
Frequently Asked Questions (FAQs)
Q1. Is this job suitable for freshers?
Yes, candidates with 6 months of experience or relevant internships can apply. Freshers with strong academic knowledge may also be considered.
Q2. What skills are important for this role?
Attention to detail, data accuracy, basic clinical research knowledge, and communication skills are essential.
Q3. What is the career growth after this role?
You can move into roles like Clinical Research Associate, Data Manager, or Pharmacovigilance Specialist.
Q4. Is prior experience in oncology required?
No, but basic knowledge of clinical research and willingness to learn is important.
