Looking for a career in clinical research contracts and proposals? A promising opportunity is now open at Cliantha Research for the role of Central Contracts & Proposal (BA/BE) in Ahmedabad. This role is ideal for B.Pharm and B.Sc graduates with 1โ2 years of experience in BA/BE studies, CRO proposal preparation, and contract management.
If youโre aiming to grow in the clinical research organization (CRO) industry, this position offers hands-on exposure to feasibility analysis, proposal development, and regulatory-compliant contract handling.
Job Overview
- Role: Central Contracts & Proposal โ BA/BE
- Company: Cliantha Research
- Experience: 1โ2 Years
- Salary: โน3,00,000 โ โน5,00,000 per annum
- Location: Ahmedabad, Gujarat
- Employment Type: Full-Time, Permanent
- Industry: Clinical Research / CRO
Key Responsibilities
As part of the contracts and proposal team in BA/BE studies, your responsibilities will include:
- Initiating feasibility assessments with internal technical teams
- Tracking and following up on feasibility status
- Preparing BA/BE proposals, quotations, and documentation
- Drafting and reviewing pre-study and study-related contracts
- Managing contract modifications and change orders
- Revising scope of work and budget adjustments
- Coordinating with cross-functional teams for timely delivery
This role demands strong exposure to clinical trial proposal preparation and contract lifecycle management.
Required Qualifications
To qualify for this BA/BE contracts job in Ahmedabad, candidates should have:
- Education: B.Pharm or B.Sc (Life Sciences or related field)
- Experience: 1โ2 years in contracts and proposals (BA/BE studies preferred)
- Knowledge of regulatory guidelines for BA/BE studies
- Strong organizational and planning skills
- Excellent English communication and documentation ability
- Ability to work independently and manage multiple priorities
Preferred Skills
- Proposal preparation and budgeting
- Contract drafting and negotiation
- Forecasting and financial understanding
- CRO operations and clinical research workflows
Benefits of Working at Cliantha Research
- Opportunity to work with a global CRO
- Exposure to USFDA, EMA, DCGI regulated studies
- Career growth in clinical research and regulatory domain
- Collaborative and professional work environment
- Hands-on experience with end-to-end proposal and contract management
About Cliantha Research
Cliantha Research is a full-service Clinical Research Organization (CRO) specializing in:
- BA/BE studies and Phase IโIV trials
- Respiratory, dermatology, and consumer research
- Biometrics, IVRT, and medical services
With operations across India, USA, and Canada, Cliantha has been inspected by major regulatory bodies like USFDA, EMA, and DCGI, making it a trusted name in clinical development.
How to Apply
