Cliantha Research is hiring pharmaceutical and clinical research professionals for two roles in Ahmedabad โ Central Contracts & Proposal โ BA/BE and Medical Writer.
These Cliantha Research jobs are relevant for candidates with qualifications including B.Pharm, M.Pharm and M.Sc, subject to the educational and experience requirements of the individual position. The openings involve BA/BE study proposals, contracts, budgeting, protocol writing, informed consent documents, regulatory documentation and coordination with clinical study teams.
Candidates looking for B.Pharm jobs in Ahmedabad, M.Pharm jobs, medical writer jobs, BA/BE clinical research jobs, proposal jobs or CRO jobs in Ahmedabad can review the eligibility details below.
Vacancy Overview
| Role | Qualification | Experience | Salary |
|---|---|---|---|
| Central Contracts & Proposal โ BA/BE | B.Pharm / M.Sc | 1โ2 Years | โน3.5โ4.5 LPA |
| Medical Writer | B.Pharm / M.Pharm | 2โ4 Years | โน4โ5 LPA |
Number of Openings: 1 per role as listed in the provided job postings
Job Location: Ahmedabad
Work Type: Full-Time, Permanent
Medical Writer Work Mode: On-site
Role 1: Central Contracts & Proposal โ BA/BE
Cliantha Research is looking for a pharmaceutical graduate with relevant experience in contracts and proposals for BA/BE studies. The position focuses on feasibility assessment, proposal and quotation preparation, study contracts, costing, budgeting and change orders.
Key Responsibilities
- Review new client inquiries and initiate feasibility assessments with the internal technical team.
- Follow up with relevant teams and track BA/BE study feasibility.
- Prepare BA/BE proposals and quotations based on project requirements.
- Prepare and maintain proposal documentation.
- Develop and review pre-study and study-related contracts for BA/BE studies.
- Provide appropriate comments and responses during contract review.
- Prepare contract modifications and change orders.
- Coordinate revisions to the scope of work.
- Support study budget modifications and related commercial documentation.
- Manage multiple priorities while maintaining accurate documentation and timelines.
Eligibility & Qualifications
Education: B.Pharm candidates are specifically listed at the undergraduate level, while M.Sc candidates are listed at the postgraduate level.
Experience: 1โ2 years, with preference for candidates having experience in BA/BE contracts and proposals.
Candidates should have:
- Knowledge of basic regulatory guidelines governing BA/BE studies.
- Strong planning and organizational skills.
- Ability to work independently and handle multiple priorities.
- Excellent English communication skills.
- Good customer service and stakeholder coordination capabilities.
- Ability to understand and apply information from technical documents and manuals.
Preferred Skills
Relevant skills include BA/BE proposals, study contracts, study proposals, costing, budgeting, forecasting and techno-commercial activities.
Role 2: Medical Writer
The Medical Writer job at Cliantha Research Ahmedabad involves developing essential clinical study and regulatory documents while coordinating with investigators, biostatisticians, analytical teams, sponsors and Ethics Committees.
The position is particularly suitable for experienced B.Pharm and M.Pharm professionals interested in clinical research medical writing and protocol writing.
Key Responsibilities
- Prepare clinical study protocols according to applicable regulatory requirements.
- Develop Informed Consent Documents (ICDs) and Case Report Forms (CRFs).
- Prepare other protocol-related clinical study documents.
- Coordinate with the Group In-charge, Principal Investigator, Biostatistician, Analytical Investigator and department leadership.
- Work with study personnel and other departments to resolve protocol-related issues.
- Coordinate protocol finalization.
- Support approval of protocols from the Ethics Committee in consultation with the Principal Investigator and sponsor.
- Translate Gujarati Informed Consent Documents from English into Gujarati.
- Communicate protocol-related concerns to investigators, sponsors and Ethics Committees.
- Prepare and revise relevant Standard Operating Procedures (SOPs).
- Complete required role-specific training and maintain awareness of applicable SOPs.
- Stay updated on pharmaceutical and clinical research regulatory requirements, including FDA expectations, GCP and GLP.
Medical Writer Eligibility
Qualification: B.Pharm / M.Pharm
Experience: 2โ4 years
Candidates should ideally have practical experience in medical writing, protocol preparation, clinical research documentation and regulatory documents.
Knowledge of BA/BE studies, GCP, clinical protocols and Clinical Study Reports can strengthen the candidate’s suitability for the role.
Why Consider These Cliantha Research Jobs?
These openings provide opportunities to develop specialized careers within the clinical research and CRO industry.
The Central Contracts & Proposal role provides exposure to feasibility assessment, client proposals, contracts, study budgets and commercial aspects of BA/BE projects. This can be useful for professionals interested in clinical research business operations and proposal management.
The Medical Writer role provides experience with clinical protocols, informed consent documents, CRFs, Ethics Committee processes, SOPs and regulatory documentation.
Additional advantages include:
- Full-time, permanent employment.
- Experience within the clinical research/CRO environment.
- Exposure to BA/BE studies.
- Cross-functional collaboration with technical and clinical research teams.
- Opportunities to strengthen regulatory and clinical documentation expertise.
- Career development in specialized pharmaceutical and clinical research functions.
Who Should Apply?
Candidates may consider applying if they match the requirements for either position.
For Central Contracts & Proposal โ BA/BE, the strongest fit is a Pharma graduate with prior experience handling BA/BE proposals, contracts, quotations, budgets or related commercial documentation.
For the Medical Writer opening, B.Pharm or M.Pharm professionals with 2โ4 years of relevant medical writing experience and knowledge of protocols, GCP and clinical research documentation are preferred.
Applicants should carefully verify that their education, experience and skills align with the specific position before submitting an application.
How to Apply
Application Link For Central Contracts & Proposal- BA/BE
Application Link For Medical Writer



