Cliantha Research Hiring Medical Writing, Process Excellence IT & Contract

BPharm MPharm Clinical Research Jobs Ahmedabad – Cliantha

Cliantha Research hiring Medical Writing, Process Excellence IT & Contract roles in Ahmedabad. BPharm, MPharm eligible. 3 vacancies.

Cliantha Research Limited has announced multiple mid-level openings at its Ahmedabad facility across Medical Writing, Process Excellence (IT), and Contract & Proposal functions. These roles are ideal for pharmaceutical and clinical research professionals seeking structured growth within a globally recognized CRO environment. With a strong footprint in BA/BE studies and early-phase clinical research, Cliantha offers meaningful roles that directly support regulatory submissions, clinical operations, and process innovation.

Clinical research careers are increasingly driven by regulatory precision, documentation quality, and operational efficiency. The current hiring reflects Cliantha’s focus on strengthening core scientific and process excellence teams that enable compliant, high-quality research outcomes for global sponsors.

Company Overview

Cliantha Research Limited is a well-established Contract Research Organization (CRO) providing end-to-end clinical research services, with particular strength in BA/BE studies, early-phase research, and regulatory-compliant documentation. The organization works closely with pharmaceutical, biotechnology, and healthcare companies across domestic and international markets.

With a strong emphasis on ethics, regulatory adherence, and scientific accuracy, Cliantha has built a reputation for reliability in clinical operations. The Ahmedabad center serves as a key hub for medical writing, clinical operations support, feasibility, contracts, and process excellence functions. Professionals at Cliantha gain exposure to sponsor interactions, ethics committee processes, and cross-functional clinical research workflows.

Job Role & Responsibilities

1. Medical Writing – BA/BE Studies

Medical Writers will be responsible for developing and managing clinical documents related to bioavailability and bioequivalence studies.

Key Responsibilities:

• Designing and preparing clinical study protocols
• Developing Case Report Forms (CRFs) and Informed Consent Documents (ICDs)
• Preparing protocol-related documents in coordination with investigators and group-in-charge
• Managing interdepartmental and intradepartmental communication
• Coordinating protocol submissions and approvals with sponsors and Ethics Committees
• Ensuring regulatory compliance and documentation accuracy

This role is suited for professionals targeting medical writing jobs in clinical research and BA/BE study documentation roles.

2. Process Excellence – IT Specialist

The Process Excellence IT Specialist will focus on optimizing IT-driven processes across clinical research operations.

Key Responsibilities:

• Conducting gap analysis of IT infrastructure and related processes
• Aligning Clinical Operations workflows with IT systems
• Supporting process optimization and digital transformation initiatives
• Ensuring regulatory compliance through efficient system design
• Driving smart technology adoption across clinical research functions

This position aligns with high-demand clinical research process excellence and IT compliance roles.

3. Contract & Proposal – Early Phase

This role supports feasibility, contracting, and proposal development for early-phase and BA/BE studies.

Key Responsibilities:

• Initiating feasibility assessments with technical and operational teams
• Tracking feasibility progress and coordinating follow-ups
• Preparing BA/BE proposals, quotations, and supporting documents
• Developing proposal narratives and client-facing documents
• Supporting early-phase business development activities

This role is ideal for candidates seeking contract and proposal jobs in CROs and early-phase clinical research support roles.

Eligibility / Qualifications

Educational Qualifications

• B.Pharmacy
• M.Pharmacy
• M.Sc. (Life Sciences or related disciplines)

(Relevant courses: BPharm, MPharm – Pharmaceutics, Pharmacology, Regulatory Affairs, MSc Life Sciences)

Experience Requirements

• Medical Writing – BA/BE: 2–5 years
• Process Excellence – IT Specialist: 4–6 years
• Contract & Proposal – Early Phase: 1–3 years

Required Skills

• Strong understanding of clinical research processes
• Knowledge of regulatory documentation and compliance
• Effective communication and cross-functional coordination
• Process analysis and documentation skills
• Ability to work in a regulated CRO environment

These skills map closely to high-CPC clinical research and CRO job searches.

Location & Salary

Job Location: Ahmedabad, Gujarat

Salary: Compensation will be competitive and aligned with industry standards, depending on role, experience, and technical expertise. Cliantha Research offers structured growth, exposure to global sponsors, and long-term career development in clinical research.

Application Process

Interested candidates should share their updated CV via email.

Apply Here: recruitment1@cliantha.com

Candidates are advised to use a clear and relevant subject line mentioning the role applied for to ensure faster screening.

Why Build Your Career at Cliantha Research

• Established CRO with strong BA/BE and early-phase expertise
• Exposure to regulatory submissions and ethics committee processes
• Cross-functional learning across clinical, IT, and business support roles
• Stable organization with compliance-driven culture
• Direct contribution to safe, ethical clinical research

These opportunities are suitable for candidates searching for clinical research jobs in Ahmedabad, medical writing roles, CRO process excellence positions, and contract & proposal jobs in clinical research.

FAQs

Who can apply for these roles?

Candidates with B.Pharm, M.Pharm, or relevant MSc qualifications and the required experience can apply.

Are freshers eligible?

No. All roles require prior clinical research or relevant functional experience.

Is prior BA/BE experience mandatory?

Yes, for Medical Writing and Contract & Proposal roles, BA/BE exposure is preferred.

Is there any application or recruitment fee?

No. Cliantha Research does not charge any fees at any stage of recruitment.

Summary Table

Company	Cliantha Research Limited
Vacancies	Medical Writer – BA/BE, Process Excellence IT Specialist, Contract & Proposal – Early Phase
Required Education	B.Pharm, M.Pharm, M.Sc.
Experience	1–6 years (role dependent)