Cliantha Research Hiring Freshers & Experienced – Multiple Roles
Are you seeking Cliantha Research careers in Ahmedabad, clinical research freshers jobs in Gujarat, or CRO vacancies for B.Pharm, M.Pharm, and Life Sciences? Leading global clinical research organization (CRO) Cliantha Research has announced multiple job openings for both freshers and experienced professionals across its Ahmedabad and Vadodara hubs.
This medical monitoring, systematic bioanalytical QA/QC testing, global compliance auditing, clinical research proposals development, protocol medical writing, biostatistics, and regulatory affairs recruitment is open to science, medical, and management graduates. The available roles accept B.Pharm, M.Pharm, M.Sc (Statistics / Life Sciences), Pharm.D, MBA, MBBS, and MD Pharmacology degrees. Depending on the specific vacancy, the required experience ranges from 0 years (freshers) up to 7 years. To learn how to structure your clinical study logs, laboratory methodologies, or research project outlines into a high-quality format, read our guide on how to apply for healthcare and pharma jobs.
📋 Job Overview
- Company: Cliantha Research
- Industry: Clinical Research Organization (CRO)
- Job Type: Full-Time
- Experience: Freshers to 7 Years (Depending on role)
- Locations: Ahmedabad & Vadodara, Gujarat, India
- Qualifications: B.Pharm / M.Pharm / Pharm.D / M.Sc / MBA / MBBS / MD Pharmacology
- Apply Mode: Email Application (jobs@cliantha.com)
- Last Date to Apply: Apply at the earliest
💼 Latest Job Openings & Qualifications
-
1. Medical Monitor (Fresher)
Location: Ahmedabad
Qualification: MBBS / MD Pharmacology
Experience: 0 Years (Freshers Eligible) -
2. Regulatory Affairs (0 – 1 Year)
Location: Ahmedabad
Qualification: B.Pharm
Experience: 0 – 1 Year in Clinical Research -
3. Clinical Physician (0 – 2 Years)
Location: Vadodara
Qualification: MBBS
Experience: 0 – 2 Years in Clinical Research -
4. Proposal Developer (2 – 3 Years)
Location: Ahmedabad
Qualification: B.Pharm / M.Pharm
Experience: 2 – 3 Years in proposal tracking -
5. Business Development (2 – 4 Years)
Location: Ahmedabad
Qualification: B.Pharm / MBA
Experience: 2 – 4 Years in healthcare BD -
6. QA/QC – Bioanalytical Lab (2 – 4 Years)
Location: Ahmedabad
Qualification: B.Pharm / M.Pharm / M.Sc
Experience: 2 – 4 Years in bioanalytical operations -
7. Medical Writer (2 – 4 Years)
Location: Ahmedabad
Qualification: M.Pharm (Pharmacology) / Pharm.D
Experience: 2 – 4 Years in Protocol Writing -
8. Biostatistician (2 – 4 Years)
Location: Ahmedabad
Qualification: M.Sc (Statistics)
Experience: 2 – 4 Years in biostatistics -
9. Global Compliance Auditor (5 – 7 Years)
Location: Ahmedabad
Qualification: B.Pharm / M.Pharm / M.Sc
Experience: 5 – 7 Years in Clinical Research audits
⚙ Key Responsibilities
- Bioanalytical QA/QC: Verify and review analytical data, validations, and laboratory procedures in compliance with GLP.
- Medical Monitoring: Support clinical trial teams by assessing safety parameters and reviewing clinical trial protocols.
- Proposal and BD Management: Structure cost estimates, compile bid dossiers, and manage communications with sponsors.
- Regulatory Documentation: Support submission strategies, dossier compilations, and ensure documentation compliance with guidelines.
- Medical Writing: Draft high-quality clinical trial protocols, Investigator Brochures (IB), and clinical study reports.
- Compliance Auditing: Conduct internal and clinical site audits to ensure complete alignment with GCP and regulatory requirements.
To learn about submission formats, dossier review processes, and agency workflows, read our guide on how to Crack Your Regulatory Affairs Interview.
🎓 Eligibility Criteria
- Education: Bachelor's or Master's degree in Pharmacy, Medical Sciences (MBBS/MD), Life Sciences (M.Sc), Statistics, or an MBA.
- Experience Range: Varies from Fresher level up to 7 years, depending on the role.
- Clinical Knowledge: Familiarity with ICH-GCP guidelines, GLP standards, and corporate clinical workflows.
- Communication: Good written and verbal English communication skills for working with global sponsors.
For pharmacy graduates interested in planning their career paths across clinical trial sites or CROs, explore the comparison guide on B.Pharm Careers in India vs USA.
🎁 Why Join Cliantha Research?
- Work with a leading, globally recognized CRO handling phase I-IV clinical trials.
- Access diverse career pathways spanning QA, biostatistics, medical writing, and clinical operations.
- Collaborate with international sponsors and global pharmaceutical teams.
- Structured peer mentoring, competitive benefits, and a stable work culture.
If you want to prepare for database validation or document quality check questions, review our guide on Clinical Data Management (CDM) Interview Questions.
📝 Resume Tips for Cliantha Research Candidates
- Tailor to the Role: If applying for Bioanalytical QA, emphasize GLP knowledge. If applying for Medical Writing, detail your protocol drafting projects.
- Mention GCP Concepts: Use key terms like ICH-GCP, GLP, SOP, eTMF, Protocol Remediation, and CAPA in your skill listings.
- Format Your Submission: Make sure your email text is professional and clear when sending your CV to the recruitment mailbox.
💬 Cliantha Research Interview Questions
- Q1. What is the role of a Medical Monitor in clinical trials?
Answer Guidance: A Medical Monitor serves as the primary medical contact for clinical trial sites. They verify protocol eligibility, assess patient safety issues, evaluate serious adverse events (SAEs), and provide medical oversight to ensure compliance with trial guidelines. - Q2. Explain the difference between Quality Assurance (QA) and Quality Control (QC) in a bioanalytical lab.
Answer Guidance: QC is a process-oriented activity focused on identifying errors or deviations during tests (e.g., verifying sample logs). QA is a systems-oriented activity focused on establishing standard procedures and auditing workflows to ensure errors do not occur. - Q3. What are the key elements included in a Clinical Trial Protocol?
Answer Guidance: A clinical trial protocol contains the study objectives, design, inclusion and exclusion criteria, treatment plans, efficacy and safety assessment methods, statistical methodologies, and ethical considerations in line with GCP.
📖 How to Apply?
Before submitting your application, please read our step-by-step guidance on how to format your application profile and navigate the hiring processes:
📧 Email Application Process
This is an Email Application. Send your updated resume directly to the recruitment team:
- Email Address: jobs@cliantha.com
- Subject Line Format: Application for [Insert Role Name] - [Insert Experience in Years]
- Cover Letter Note: Briefly write about your key qualifications and current location in the email body.
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🚀 Launch Free ATS Resume Tool❓ Frequently Asked Questions
Q. Are freshers eligible to apply at Cliantha Research?
Yes, freshers can apply. The Medical Monitor (MBBS/MD Pharmacology) and Regulatory Affairs (0-1 year, B.Pharm) openings accept entry-level candidates.
Q. How should I submit my application?
Interested candidates must submit their updated resume by email to jobs@cliantha.com with a clear subject line indicating the target role.
Q. Where are these job openings based?
The positions are based at Cliantha Research's facilities in Ahmedabad and Vadodara, Gujarat.
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