Clinical Research Coordinator (CRC) Jobs 2026 | TULIPHALL CliniResearch Private Limited Hiring for Kolkata & Bangalore

Are you an experienced Clinical Research professional looking for your next career opportunity? Here’s an excellent opening from TULIPHALL CliniResearch Private Limited (TCRPL) for Clinical Research Coordinator (CRC) positions in Kolkata and Bangalore.

If you have at least one year of hands-on clinical trial experience and want to work with a growing clinical research organization, this recruitment drive could be the perfect opportunity to advance your career. Immediate joiners are strongly preferred, making this an ideal chance for professionals ready to take the next step.

📌 Job Overview

Particular	Details
Organization	TULIPHALL CliniResearch Private Limited (TCRPL)
Position	Clinical Research Coordinator (CRC)
Job Type	Full-Time
Experience	Minimum 1 Year
Qualification	M.Sc. (Life Sciences), B.Pharm, M.Pharm or Equivalent
Locations	Kolkata & Bangalore
Vacancies	2 (1 each location)
Preference	Immediate Joiners

🏢 About TULIPHALL CliniResearch Private Limited

TULIPHALL CliniResearch Private Limited (TCRPL) is involved in providing clinical research solutions and supporting clinical trial operations across multiple therapeutic areas. The company focuses on maintaining high-quality standards, regulatory compliance, and ethical conduct throughout the clinical research process.

Clinical Research Coordinators at TCRPL work closely with investigators, sponsors, ethics committees, and study participants to ensure smooth execution of clinical studies.

📍 Job Locations

🌆 Kolkata – 1 Opening
🌆 Bangalore – 1 Opening

🎓 Educational Qualification

Candidates should possess any of the following qualifications:

✅ M.Sc. (Life Sciences)
✅ B.Pharm
✅ M.Pharm
✅ Equivalent Life Science Degree

💼 Experience Required

Applicants must have:

Minimum 1 year of clinical trial experience
Practical exposure to site-level clinical trial activities
Understanding of GCP guidelines and clinical research documentation
Ability to join immediately will be an added advantage

Freshers are not eligible for this position.

📝 Key Responsibilities

The selected candidates may be responsible for:

Coordinating clinical trial activities at the study site
Scheduling patient visits and follow-ups
Maintaining Investigator Site Files (ISF)
Managing essential study documentation
Supporting informed consent procedures
Assisting investigators during study visits
Maintaining source documents and CRFs
Coordinating with sponsors and Clinical Research Associates (CRAs)
Ensuring protocol compliance
Reporting adverse events when applicable
Supporting monitoring visits, audits, and inspections
Maintaining accurate trial records
Assisting with regulatory documentation

⭐ Required Skills

Successful candidates should possess:

Excellent communication skills
Good documentation practices
Knowledge of ICH-GCP guidelines
Strong organizational abilities
Attention to detail
Time management skills
Teamwork and coordination
Problem-solving mindset
Basic computer proficiency
Ability to manage multiple studies simultaneously

📈 Career Growth

Working as a Clinical Research Coordinator provides opportunities to progress into roles such as:

Clinical Research Associate (CRA)
Senior CRC
Clinical Trial Manager
Clinical Operations Executive
Clinical Project Manager
Regulatory Affairs Professional
Clinical Data Manager
Pharmacovigilance Associate

💡 Resume Tips

Before applying:

Update your latest work experience.
Mention therapeutic areas handled.
Highlight GCP certification.
Include responsibilities during monitoring visits.
Mention regulatory documentation experience.
Add achievements and performance metrics wherever possible.
Ensure your contact details are up to date.

📧 How to Apply

Interested and eligible candidates should email the following documents:

Updated Resume/CV
Current CTC
Expected CTC

Email: research@tcrpl.com

Apply as early as possible since the hiring is on a First Come, First Served basis and immediate joiners are preferred.

❓ Frequently Asked Questions (FAQs)

Is this job open for freshers?

No. Candidates must have a minimum of one year of clinical trial experience.

What is the minimum qualification?

M.Sc. (Life Sciences), B.Pharm, M.Pharm, or an equivalent Life Science qualification.

Where are the job locations?

Kolkata and Bangalore.

How many vacancies are available?

There are two vacancies—one in Kolkata and one in Bangalore.

Is GCP knowledge required?

Yes. Familiarity with Good Clinical Practice (GCP) guidelines is highly desirable.

How can I apply?

Send your updated CV along with your current and expected CTC to research@tcrpl.com.

📢 Final Words

The demand for experienced Clinical Research Coordinators continues to grow as India’s clinical research industry expands rapidly. If you already have experience working in clinical trials and are looking for an opportunity to grow with a professional research organization, TULIPHALL CliniResearch Private Limited offers an excellent platform to enhance your career.

Since the organization is giving preference to immediate joiners and following a first-come, first-served selection process, eligible candidates are encouraged to submit their applications without delay.

Best of luck with your application!