Clinical Research Coordinator (CRC) 2026 | TULIPHALL CliniResearch Private

Clinical Research Coordinator (CRC) Jobs 2026 | TULIPHALL CliniResearch Private Limited Hiring [.]

Company: Jobs On The Way

Job Location: Bengaluru, Karnataka, India

Employment Type: Full-time

Experience Required: 1+ years

Salary: 4L5.5L a year

Are you an experienced Clinical Research professional looking for your next career opportunity Heres 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 handson 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 highquality 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

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 sitelevel 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 followups

Managing essential study documentation

Supporting informed consent procedures

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

Good documentation practices

Knowledge of ICHGCP guidelines

Strong organizational abilities

Teamwork and coordination

Problemsolving mindset

Basic computer proficiency

Ability to manage multiple studies simultaneously

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

Mention therapeutic areas handled.

Highlight GCP certification.

Mention regulatory documentation experience.

Add achievements and performance metrics wherever possible.

Ensure your contact details are up to date.

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 vacanciesone in Kolkata and one in Bangalore.

Is GCP knowledge required

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

The demand for experienced Clinical Research Coordinators continues to grow as Indias 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 firstcome, firstserved selection process, eligible candidates are encouraged to submit their applications without delay. .