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Associate Scientist : Clinical Unit - Cro

Lupin
lupin
5-7 years
preferred by company
10 Feb. 11, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate Scientist – Clinical Unit (CRO / BA-BE Studies)

Location: Pune LBC, Maharashtra, India
Company: Lupin
Date Posted: January 19, 2026
Employment Type: Full-Time
Industry: Clinical Research | Contract Research Organization (CRO) | BA-BE Studies


About the Role

Lupin is seeking an experienced Associate Scientist – Clinical Unit to oversee outsourced and in-house BA-BE studies in alignment with regulatory guidelines and company protocols. The role involves monitoring clinical studies at external CROs, coordinating study execution, and ensuring accurate documentation and data integrity throughout the clinical research process.

This position is ideal for candidates with a strong background in clinical research coordination, CRO management, and bioavailability/bioequivalence study execution.


Experience Required

  • 5–7 years of relevant experience in clinical research or BA-BE study monitoring

  • Hands-on experience with outsourced CRO studies, clinical study coordination, and regulatory compliance


Educational Qualification (Mandatory)

  • Postgraduate degree (M.Pharm / Masters in Pharmacy)


Key Responsibilities

CRO & Clinical Study Monitoring

  • Monitor outsourced BA-BE studies at external CROs according to protocol and regulatory guidelines

  • Coordinate with CRO representatives for technical discussions and study updates

  • Review clinical documentation including Trial Master File (TMF), screening MSRs, Informed Consent Documents (ICD), CRFs, dosing logs, sample collection, and processing records

In-House Clinical Study Coordination

  • Plan, execute, and supervise in-house BA-BE studies as a Clinical Research Coordinator

  • Conduct protocol training for study teams and ensure TMF compilation

  • Prepare study updates, resolve study queries, and maintain proper documentation of raw data

Regulatory & Data Compliance

  • Ensure clinical studies comply with applicable regulatory guidelines and company SOPs

  • Maintain accurate records and ensure data integrity and audit readiness

  • Support quality and compliance audits related to clinical study operations


Required Skills & Competencies

  • Strong understanding of clinical research operations, BA-BE study design, and CRO management

  • Experience with Trial Master File (TMF) management, CRF review, and study documentation

  • Proficient in clinical study planning, execution, and data analysis

  • Excellent interpersonal, communication, and coordination skills

  • Ability to work independently and collaboratively in a regulated environment

Core Competencies

  • Collaboration & Cross-Functional Alignment

  • Process Excellence & Compliance

  • Result Orientation & Accountability

  • Stakeholder Management

  • Customer Centricity


Why Join Lupin?

  • Work on outsourced and in-house clinical BA-BE studies in a regulated environment

  • Gain exposure to CRO collaboration, clinical study monitoring, and regulatory compliance

  • Build expertise in clinical research coordination and documentation management

  • Contribute to high-quality bioavailability and bioequivalence studies


Equal Opportunity Statement

Lupin is committed to providing equal employment opportunities across recruitment, promotion, compensation, and professional development. All qualified candidates will be considered in accordance with applicable regulatory and employment standards.