Introduction
The clinical research industry in India is witnessing unprecedented growth, creating thousands of opportunities for professionals from Life Sciences, Pharmacy, Biotechnology, Nursing, and Healthcare backgrounds. As pharmaceutical companies, biotechnology firms, and Contract Research Organizations (CROs) continue to invest heavily in clinical trials, the demand for skilled Clinical Research Coordinators (CRCs) is steadily increasing.
If you are looking to build a rewarding career in clinical research and gain hands-on experience in managing clinical trials, participant coordination, regulatory compliance, and study documentation, then this opportunity could be ideal for you.
CYTENET SMO, a reputed Site Management Organization (SMO), is currently inviting applications for the position of Clinical Research Coordinator (CRC) at its Ahmedabad location. This role offers an excellent opportunity for candidates with clinical research experience as well as individuals who have completed relevant internships or clinical research training programs.
In this detailed article, we will explore the job responsibilities, eligibility criteria, career prospects, required skills, benefits, and application process for the Clinical Research Coordinator vacancy at CYTENET SMO.
About CYTENET SMO
CYTENET SMO is a specialized Site Management Organization that supports clinical trial operations by working closely with investigators, sponsors, healthcare institutions, and Contract Research Organizations (CROs).
The organization focuses on ensuring that clinical studies are conducted efficiently while maintaining the highest standards of patient safety, regulatory compliance, and data integrity.
Through its expertise in clinical trial management, patient recruitment, study coordination, and regulatory documentation, CYTENET SMO contributes significantly to the successful execution of clinical research projects across multiple therapeutic areas.
As the clinical research industry expands in India, organizations like CYTENET SMO continue to play an important role in advancing healthcare innovation and supporting the development of new medicines and treatments.
Job Details
| Particulars | Information |
|---|---|
| Position | Clinical Research Coordinator (CRC) |
| Company | CYTENET SMO |
| Location | Ahmedabad, Gujarat |
| Job Type | Full-Time |
| Vacancies | 01 |
| Experience | 1 to 1.5 Years Preferred |
| Qualification | Life Sciences, Pharmacy, Nursing, Biotechnology, Healthcare |
| Application Mode | Email Application |
Why Choose a Career as a Clinical Research Coordinator?
Clinical Research Coordinators are among the most important professionals involved in clinical trial operations.
They act as the primary link between:
- Principal Investigators
- Study Participants
- Sponsors
- CROs
- Ethics Committees
- Regulatory Authorities
A CRC ensures that every aspect of a clinical study is conducted according to approved protocols, ethical guidelines, and regulatory requirements.
This position provides valuable exposure to various aspects of clinical research and serves as an excellent stepping stone toward advanced roles such as:
- Clinical Research Associate (CRA)
- Senior Clinical Research Coordinator
- Clinical Trial Manager
- Clinical Operations Manager
- Regulatory Affairs Specialist
- Project Manager
Key Responsibilities
The selected candidate will play a critical role in ensuring smooth clinical trial execution.
1. Clinical Trial Coordination
The Clinical Research Coordinator will manage day-to-day study activities and ensure that trial procedures are performed according to protocol requirements.
Responsibilities include:
- Coordinating study schedules
- Managing participant appointments
- Monitoring study timelines
- Assisting investigators
- Ensuring protocol adherence
Effective coordination helps maintain study quality and ensures project milestones are achieved.
2. Patient Recruitment and Enrollment
Recruiting suitable participants is one of the most important tasks in clinical research.
The CRC will:
- Review eligibility criteria
- Identify potential participants
- Conduct initial screenings
- Schedule assessments
- Support participant enrollment
Efficient recruitment contributes significantly to study success.
3. Informed Consent Process
Participant safety and ethical compliance are fundamental principles of clinical research.
The CRC supports investigators in:
- Explaining study procedures
- Discussing benefits and risks
- Addressing participant concerns
- Documenting informed consent
Proper consent procedures ensure participants fully understand the study before enrollment.
4. Study Visit Management
Clinical studies often require multiple participant visits.
The coordinator will:
- Schedule visits
- Conduct follow-ups
- Track participant compliance
- Manage visit documentation
- Coordinate study-related procedures
Well-organized visit management improves participant retention and data quality.
5. Data Collection and Documentation
Accurate documentation is essential for maintaining research integrity.
Responsibilities include:
- Recording participant data
- Maintaining source documents
- Verifying information accuracy
- Supporting data entry activities
- Resolving discrepancies
Reliable data forms the foundation of successful clinical research.
6. Regulatory Compliance
Clinical studies must comply with national and international regulations.
The CRC will ensure compliance with:
- Good Clinical Practice (GCP)
- ICH Guidelines
- Institutional Policies
- Sponsor Requirements
- Regulatory Standards
Compliance helps protect participant rights and study credibility.
7. Investigator Site File Maintenance
Maintaining organized study documentation is crucial.
The coordinator will manage:
- Investigator Site Files (ISF)
- Regulatory Binders
- Protocol Documents
- Ethics Committee Approvals
- Training Records
Proper documentation facilitates successful audits and inspections.
8. Ethics Committee Support
The Ethics Committee oversees participant safety and study ethics.
The CRC will assist with:
- Ethics submissions
- Amendment submissions
- Document compilation
- Approval tracking
- Communication management
Timely submissions prevent unnecessary study delays.
9. Stakeholder Communication
Strong communication skills are essential for success.
The coordinator will interact regularly with:
- Sponsors
- CROs
- Investigators
- Study Participants
- Ethics Committees
Professional communication ensures smooth trial operations.
10. Monitoring Study Progress
The CRC will continuously evaluate study performance.
Key activities include:
- Tracking enrollment
- Monitoring retention
- Identifying protocol deviations
- Reporting issues
- Supporting corrective actions
Continuous monitoring helps maintain study quality.
11. Audit and Inspection Support
Clinical research sites undergo regular evaluations.
The selected candidate may participate in:
- Site Selection Visits
- Site Initiation Visits
- Monitoring Visits
- Internal Audits
- Regulatory Inspections
- Site Close-Out Visits
This experience enhances professional growth and industry exposure.
Eligibility Criteria
Educational Qualifications
Candidates should possess one of the following qualifications:
- B.Pharm
- M.Pharm
- B.Sc Life Sciences
- M.Sc Life Sciences
- B.Sc Biotechnology
- M.Sc Biotechnology
- Nursing Degree
- Healthcare Sciences Degree
- Related Scientific Qualification
Candidates with strong academic backgrounds will be preferred.
Experience Requirements
Preferred candidates should have:
- 1 to 1.5 years of clinical research experience
- Experience working at research sites
- Knowledge of clinical trial procedures
- Familiarity with patient recruitment
- Exposure to study documentation
Can Freshers Apply?
Yes.
Freshers with:
- Clinical research internships
- Clinical research certifications
- GCP training
- Site management experience
may also be considered depending on their profile and skills.
Skills Required
Successful Clinical Research Coordinators typically possess the following competencies:
Technical Skills
- Good Clinical Practice (GCP)
- ICH-GCP Guidelines
- Clinical Trial Documentation
- Microsoft Excel
- Microsoft Word
- Microsoft PowerPoint
- CTMS Knowledge
- EDC Systems Knowledge
Soft Skills
- Communication Skills
- Teamwork
- Organization Skills
- Attention to Detail
- Time Management
- Problem Solving
- Multitasking
Why Ahmedabad is a Growing Hub for Clinical Research Careers
Ahmedabad has emerged as one of India’s leading pharmaceutical and biotechnology hubs.
Major advantages include:
- Presence of pharmaceutical companies
- Growing CRO sector
- Research-focused healthcare institutions
- Biotechnology ecosystem
- Increasing clinical trial activities
- Strong professional networking opportunities
As a result, clinical research professionals in Ahmedabad enjoy excellent career prospects and continuous learning opportunities.
Benefits of Joining CYTENET SMO
Working with CYTENET SMO offers several professional advantages.
Professional Growth
Employees gain practical exposure to:
- Clinical trial management
- Regulatory affairs
- Patient recruitment
- Data management
- Sponsor interactions
Learning Opportunities
The organization encourages continuous learning through:
- Training sessions
- Workshops
- Industry seminars
- Skill development programs
Industry Exposure
Employees work closely with:
- Sponsors
- CROs
- Investigators
- Ethics Committees
- Regulatory Authorities
Career Advancement
The CRC role can open doors to advanced positions within clinical research and clinical operations.
Career Opportunities After CRC Experience
Many professionals use the CRC role as a launching pad for higher positions.
Potential career paths include:
Clinical Research Associate (CRA)
Monitor multiple sites and oversee compliance activities.
Senior CRC
Lead study coordination activities and mentor junior coordinators.
Clinical Trial Manager
Manage clinical trials from initiation to completion.
Regulatory Affairs Specialist
Focus on regulatory submissions and compliance requirements.
Clinical Operations Manager
Oversee multiple projects and site operations.
Project Manager
Coordinate timelines, budgets, and resources for clinical studies.
How to Apply
Interested candidates should prepare their application carefully.
Step 1: Update Your Resume
Highlight:
- Educational qualifications
- Clinical research experience
- Internship experience
- GCP training
- Technical skills
Step 2: Prepare a Cover Letter
Include:
- Your interest in the role
- Relevant experience
- Knowledge of clinical research
- Career objectives
Step 3: Submit Your Application
Send your resume and cover letter to:
📧 Email: info@cytenet.org
Important Instruction
Include #Ahmedabad in the subject line of your email.
Example Subject:
Application for Clinical Research Coordinator – #Ahmedabad
Failure to include the city name may affect application processing.
Application Links
Apply via Email
Email ID: info@cytenet.org
Company Website
Visit the official CYTENET website for more information:
Website: https://www.cytenet.org
Final Thoughts
The Clinical Research Coordinator (CRC) Job Opening at CYTENET SMO Ahmedabad is an excellent opportunity for Life Sciences, Pharmacy, Biotechnology, Nursing, and Healthcare professionals looking to build a successful career in clinical research.
The role provides exposure to clinical trial coordination, patient management, regulatory compliance, study documentation, ethics committee interactions, and sponsor communications. Such experience is invaluable for professionals aiming to progress into advanced positions such as Clinical Research Associate, Clinical Trial Manager, or Clinical Operations Manager.
With India’s clinical research industry expanding rapidly and Ahmedabad emerging as a major pharmaceutical and research hub, this opportunity can serve as a strong foundation for long-term career growth.
Candidates who meet the eligibility criteria should apply as soon as possible and take the next step toward a rewarding future in clinical research.
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