Utopia Therapeutics Hiring Clinical Development Associate Job for MS, MPharm, MSc candidates with IND experience.
Job Type: Full Time
Location: Hyderabad, India (Hybrid)
Experience Required: 2–3 Years
Education: MS / MPharm / MSc
Industry: Clinical Development, Biotechnology, Pharmaceuticals
Application Deadline: 10 February 2026
About the Company
Utopia Therapeutics is a science-driven biotechnology company headquartered in Hyderabad, India, focused on developing first-in-class therapies in metabolic diseases and biologics. The company is actively advancing late preclinical and IND-enabling programs toward first-in-human clinical trials. Clinical Development Associate Job
Utopia Therapeutics collaborates closely with leading Contract Research Organizations (CROs), regulatory consultants, and manufacturing partners across India and the United States. With a strong translational science approach, the organization emphasizes high-quality development, regulatory readiness, and innovation-driven drug discovery. Clinical Development Associate Job
Job Details
Job Title: Clinical Development Associate
Company Name: Utopia Therapeutics
Location: Hyderabad, India
Work Mode: Hybrid
Employment Type: Full Time
Start Date: 1 February 2026
Experience Level: Mid-level (2–3 Years)
Salary Range: ₹8,00,000 – ₹12,00,000 per annum
Job Description
Utopia Therapeutics is hiring a Clinical Development Associate to support active IND-enabling programs in late preclinical development. This role is ideal for professionals with hands-on experience in clinical or preclinical development, GLP toxicology coordination, CMC documentation, and regulatory support activities. Clinical Development Associate Job
The selected candidate will work closely with senior scientists and cross-functional teams, gaining direct exposure to IND preparation and regulatory submissions. This position offers a strong foundation for career progression into Clinical Development or Regulatory Affairs. Clinical Development Associate Job
Key Responsibilities
- Coordinate GLP toxicology studies with CROs, including study timelines, progress tracking, and final reports
- Support Chemistry, Manufacturing, and Controls (CMC) readiness by compiling specifications and development data
- Assist in preparation of IND and CTA submission modules, focusing on nonclinical and CMC sections
- Manage cross-functional communication with R&D, Quality Assurance, CROs, and external partners
- Maintain regulatory-compliant documentation, development trackers, and study logs
- Support internal reviews and regulatory interactions related to IND-enabling activities
Clinical Development Associate Job
Skills / Qualifications
Educational Qualifications
- MS / MPharm / MSc in Life Sciences, Pharmacy, Biotechnology, or related disciplines
Experience Requirements
- 2–3 years of experience in clinical development, preclinical development, or regulatory support
- Practical exposure to GLP toxicology coordination and CRO management
- Experience with CMC documentation and development data compilation
- Familiarity with IND or CTA filing processes
Technical & Professional Skills
- Working knowledge of CDSCO and/or US FDA IND regulatory processes
- Strong documentation, organizational, and follow-up skills
- Ability to manage multiple deliverables and timelines effectively
- Strong communication and cross-functional coordination abilities
Clinical Development Associate Job
Benefits / Perks
- Competitive salary aligned with industry standards
- Hands-on exposure to real IND-stage drug development programs
- Opportunity to work with experienced drug developers from India and the US
- Hybrid work model offering flexibility
- Fast-paced learning environment with high ownership
Clinical Development Associate Job
Why You Should Join
- Direct involvement in late preclinical and IND-enabling drug development
- Clear career growth pathway into Clinical Development or Regulatory Affairs
- Exposure to first-in-class metabolic disease and biologics programs
- Opportunity to build strong regulatory and development expertise early in your career
- Work in a science-driven, innovation-focused biotech organization
Frequently Asked Questions (FAQs)
Who can apply for the Clinical Development Associate role?
Candidates with MS, MPharm, or MSc qualifications and 2–3 years of relevant experience can apply.
Is prior IND experience mandatory?
Direct IND filing experience is preferred but not mandatory. Exposure to IND-enabling activities is highly valued.
Is this role suitable for regulatory affairs professionals?
Yes, professionals with regulatory support experience in preclinical or clinical development are encouraged to apply.
Is the position remote or on-site?
The role follows a hybrid work model based in Hyderabad.
What therapeutic areas will I work on?
You will work on metabolic disease and biologics programs progressing toward first-in-human trials.
Clinical Development Associate Job
How to Apply
Interested and eligible candidates should apply via email.
Send your updated resume to:
accounts@utopiathx.com
Mention the subject line clearly as:
Clinical Development Associate – Hyderabad
Only shortlisted candidates will be contacted for further steps in the hiring process.
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