Cliantha Research Hiring 2026 | Medical Writer, CDM & BD Jobs Ahmedabad

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Cliantha Research Hiring 2026 – Multiple Pharma & Clinical Research Jobs

Cliantha Research is expanding its teams in Ahmedabad and is inviting applications from qualified professionals for multiple positions across Medical Writing, Clinical Data Management, Proposal Development and Business Development.

The openings are suitable for B.Pharm, M.Pharm and Pharm.D professionals with relevant experience ranging from 2 to 12 years, depending on the position.

These roles offer opportunities to work within a global Contract Research Organization (CRO) supporting clinical research and pharmaceutical development programs.

About Cliantha Research

Cliantha Research is a full-service Contract Research Organization headquartered in Ahmedabad, India, with operations spanning India, North America and Europe.

The company works across clinical research and related services, supporting pharmaceutical and healthcare organizations through scientific, clinical and regulatory activities.

Cliantha highlights its focus on “Science with Integrity”, along with a compliance-oriented and collaborative working environment.

Job Overview

Details Information
Company Cliantha Research
Location Ahmedabad, Gujarat
Industry Clinical Research / CRO
Experience 2–12 Years, depending on role
Qualifications B.Pharm / M.Pharm / Pharm.D
Work Type On-site

Current Job Openings at Cliantha Research

1. Medical Writer

Experience: 3–4 Years
Qualification: M.Pharm – Pharmacology / Pharm.D

The Medical Writer role focuses on scientific writing and medical documentation. Candidates should have relevant experience preparing and reviewing scientific documents and should be comfortable working with clinical and pharmaceutical information.

Key areas include:

  • Scientific writing
  • Medical documentation
  • Clinical and scientific content
  • Document review
  • Regulatory-compliant writing

2. Proposal Developer

Experience: 2–3 Years
Qualification: B.Pharm / M.Pharm

The Proposal Developer will support the preparation of proposals and estimates for pharmaceutical and clinical research clients.

Key areas include:

  • Proposal development
  • Cost estimation
  • Client requirements analysis
  • Coordination with internal teams
  • Preparation of business proposals

3. Clinical Data Analyst

Experience: 3–5 Years
Qualification: B.Pharm / M.Pharm / Pharm.D

This position focuses on Clinical Data Management (CDM) activities associated with clinical research studies.

Key areas include:

  • Clinical data review
  • Data validation
  • Data cleaning and analysis
  • Clinical database activities
  • Documentation and reporting

4. Senior Clinical Data Analyst

Experience: 5–6 Years
Qualification: B.Pharm / M.Pharm / Pharm.D

The Senior Clinical Data Analyst role is intended for professionals with established experience in clinical data management.

Responsibilities may include supporting senior-level CDM activities, reviewing clinical data, maintaining data quality and coordinating with project teams.

5. Business Development – Late Phase

Experience: 8–12 Years
Qualification: B.Pharm / M.Pharm / Pharm.D

This senior-level opportunity focuses on late-phase business development and client relationships within the clinical research sector.

Key areas include:

  • Business development
  • Client relationship management
  • Late-phase clinical programs
  • Proposal and commercial discussions
  • Business growth strategies

Eligibility & Skills

Candidates should have the relevant qualification and experience required for their target position.

Educational Qualifications

  • B.Pharm
  • M.Pharm
  • M.Pharm in Pharmacology for Medical Writing roles
  • Pharm.D

Core Skills

Depending on the position, candidates should have experience in:

  • Scientific and medical writing
  • Clinical Data Management
  • Clinical trial workflows
  • Proposal development and estimation
  • Pharmaceutical research processes
  • Global regulatory requirements
  • Business development and client relations
  • Cross-functional communication

Strong written and verbal communication skills are important across these roles.

Key Responsibilities

Selected professionals may be responsible for:

  • Drafting and reviewing scientific and clinical documents
  • Supporting clinical protocol and medical documentation activities
  • Reviewing and validating clinical trial data
  • Maintaining data quality and documentation
  • Preparing proposals and cost estimates
  • Coordinating with internal and client-facing teams
  • Supporting late-phase business development initiatives
  • Maintaining compliance with applicable regulatory and quality requirements

Responsibilities will vary according to the position and level of experience.

Work Environment & Career Exposure

Working in these roles can provide exposure to:

  • Global clinical research projects
  • International pharmaceutical clients
  • Clinical trial processes
  • Scientific documentation
  • Clinical data management
  • Proposal and commercial activities
  • Cross-functional CRO operations

Professionals can develop experience across different areas of the pharmaceutical and clinical research ecosystem.

Benefits & Perks

According to the supplied hiring information, candidates can expect:

  • Career development opportunities
  • Learning and professional development
  • Exposure to international clinical research projects
  • Competitive compensation
  • Collaborative work environment
  • Opportunities to work with experienced scientific and clinical professionals

How to Apply for Cliantha Research Jobs

Eligible candidates can apply by sending their updated resume/CV to:

Email: jobs@cliantha.com

Application Tip

Mention the exact position title in the email subject line, such as:

Medical Writer
Proposal Developer
Clinical Data Analyst
Senior Clinical Data Analyst
Business Development – Late Phase

This can help the recruitment team identify the position you are applying for more quickly.

Job Location

All the positions listed in this hiring drive are based in:

Cliantha Research
Ahmedabad, Gujarat, India

Frequently Asked Questions

1. What qualifications are required for Cliantha Research jobs?

Depending on the position, candidates should have a B.Pharm, M.Pharm or Pharm.D qualification.

2. What experience is required?

The advertised positions require approximately 2 to 12 years of relevant experience, depending on the role.

3. Is this hiring for freshers?

No. The listed positions require prior professional experience, ranging from 2 years to 12 years depending on seniority.

4. Which roles are currently available?

The listed openings include:

  • Medical Writer
  • Proposal Developer
  • Clinical Data Analyst
  • Senior Clinical Data Analyst
  • Business Development – Late Phase

5. Where are these jobs located?

The positions are based in Ahmedabad, Gujarat.

6. How can I apply?

Send your updated CV to jobs@cliantha.com and mention the position you are applying for in the subject line.

7. Is clinical research experience required?

Relevant experience is required for the advertised positions. The exact experience requirement varies by role.

Cliantha Research Hiring 2026

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