Senior Clinical Scientist & Trial Lead – Hybrid Role

Thepharmadaily LLP; Bristol; Hybrid; GBP 75,000 - 95,000; Full time

Job summary

A leading pharmaceutical organization is seeking an experienced Associate Director, Senior Clinical Scientist to lead clinical trial activities across multiple therapeutic programs. You will provide clinical leadership as the Clinical Trial Lead, overseeing protocol adherence and site management. The ideal candidate has over 10 years of clinical research experience, in-depth knowledge of GCP/ICH guidelines, and strong skills in clinical data review and communication. This full-time hybrid position offers a collaborative work environment and opportunities for professional development.

Benefits

Competitive benefits

Flexible work arrangements

Professional development opportunities

Qualifications

• Advanced degree in Life Sciences preferred (MD, PharmD, PhD, MS, RN).
• Minimum of 10+ years of experience in clinical research or clinical science.
• In-depth knowledge of GCP/ICH guidelines and drug development processes.

Responsibilities

• Lead planning, implementation, and management of assigned clinical trials.
• Serve as Clinical Trial Lead for overseeing protocol adherence.
• Draft, review, and validate Clinical Study Reports and regulatory documents.

Skills

Causality Assessment

Clinical SAS Programming

Communication Skills

CPC Certified

GCP guidelines

ICD-10 CM Codes

CPT-Codes

HCPCS Codes

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 ICERs

WHO DD Coding

Education

B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences

Tools

Microsoft Office

Electronic Data Capture systems (e.g., RAVE, J-Review)

Job description

A leading pharmaceutical organization is seeking an experienced Associate Director, Senior Clinical Scientist to lead clinical trial activities across multiple therapeutic programs. You will provide clinical leadership as the Clinical Trial Lead, overseeing protocol adherence and site management. The ideal candidate has over 10 years of clinical research experience, in-depth knowledge of GCP/ICH guidelines, and strong skills in clinical data review and communication. This full-time hybrid position offers a collaborative work environment and opportunities for professional development.