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Associate Director, Senior Clinical Scientist

Bristol Myers Squibb
Bristol Myers Squibb
10+ years
Not Disclosed
Hyderabad
10 March 14, 2026
Job Description
Job Type: Full Time Education: MBBS/MD 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

Job Description

Position Summary
The Associate Director, Senior Clinical Scientist is responsible for providing scientific leadership in the planning, execution, and management of clinical trials. The role supports the clinical science function by contributing to study design, trial execution, and data interpretation across clinical development programs.

This position acts as the Clinical Trial Lead for assigned studies and works closely with cross-functional teams to ensure successful study startup, conduct, and close-out activities. The role also supports regulatory interactions, clinical documentation, and scientific decision-making during the clinical development process.

Key Responsibilities

Lead and manage clinical trial activities including study startup, conduct, and close-out

Serve as Clinical Trial Lead for one or more clinical studies and coordinate trial-level execution

Maintain deep understanding of clinical study protocols and ensure proper implementation across study teams

Plan and lead interactions with local health authorities and subject expert committees

Support protocol development and informed consent form (ICF) preparation, including review and resolution of cross-functional comments

Collaborate with cross-functional teams including clinical operations, medical writing, and regulatory teams

Participate in study team meetings and provide scientific leadership to supporting clinical scientists

Support clinical development planning by analyzing clinical data and contributing to strategic decisions

Oversee clinical data generation, review, and query resolution to ensure data quality and consistency

Identify trends in clinical data and escalate relevant findings to medical monitors or leadership teams

Contribute to the preparation and review of clinical study reports (CSRs) and regulatory documentation such as Investigator Brochures and DSURs

Support training of investigators, study sites, and clinical teams during investigator meetings and study initiation visits

Professional Experience Requirements

Minimum 10 years of experience in clinical science, clinical research, or related pharmaceutical industry roles

Experience leading clinical trial activities and working with cross-functional clinical research teams

Strong knowledge of clinical trial design, drug development processes, and regulatory requirements

Experience working in oncology or hematology therapeutic areas is preferred

Familiarity with electronic data capture systems such as Medidata Rave and clinical data review tools

Strong analytical, communication, and project management skills

Apply Details

Apply via the company career portal for
Bristol Myers Squibb