GCP/ICH Guidelines jobs

Associate Director, Clinical Scientist

Bristol Myers Squibb · Posted Nov 12, 2026

Open

Uxbridge, England, United Kingdom
Hybrid
Manager
5+ years

Associate Director, Clinical Scientist

Bristol Myers Squibb · Posted Nov 12, 2026

Open

Uxbridge, England, United Kingdom
Hybrid
Manager
5+ years

Associate Director, Clinical Scientist

Bristol Myers Squibb · Posted Nov 12, 2026

Open

Uxbridge, England, United Kingdom
Hybrid
Full-time · Manager
5+ years

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Lead the planning and execution of all study activities across multiple trials, with a high degree of autonomy, providing scientific and clinical leadership to supporting Clinical Scientists.

Responsibilities

Lead the planning and execution of all study activities across multiple trials
Maintain deep protocol expertise and act as the clinical knowledge hub for your study team
Collaborate on protocol and Informed Consent Form (ICF) development
Oversee data generation and validation activities, including CRF design, clinical data review, and query resolution
Identify clinical data trends and escalate observations appropriately to the Medical Monitor

Requirements

Degree in Life Sciences
Nice to have: MD
Nice to have: PhD
Nice to have: PharmD
Nice to have: MS

Skills

GCP/ICH guidelines Drug development processes Study design Statistics Programme-specific data review Trend identification

Clinical Trial Manager

Precision for Medicine · Posted Nov 10, 2026

Open

Remote, Hungary +6 more
Remote
Full-time

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Lead and manage clinical trials across multiple countries, overseeing all clinical aspects and ensuring delivery and quality.

Locations (7)

Hungary
Poland
Romania
Serbia
Slovakia
United Kingdom

Clinical Trial Manager

Precision Medicine Group · Posted Nov 10, 2026

Open

Remote, Hungary +6 more
Remote

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Locations (7)

Hungary
Poland
Romania
Serbia
Slovakia
United Kingdom

Principal Investigator

DM CLINICAL RESEARCH GROUP · Posted Nov 10, 2026

Open

Houston, Texas, United States
2+ years

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Lead and oversee clinical research protocols, ensuring compliance with regulatory standards and protecting participant welfare.

Responsibilities

Complete DMCR-required training including GCP and IATA
Maintain knowledge of FDA regulations, GCP/ICH guidelines, SOPs, and study protocols
Maintain current CV and licensure
Assume responsibility for clinical investigation protocols
Determine resources for research

Requirements

M.D or D.O with active medical license
Board certification or eligibility in relevant specialty
Nice to have: Bilingual English/Spanish

Skills

Good Clinical Practice (GCP)IATA training FDA regulations GCP/ICH guidelines Standard Operating Procedures (SOPs)Study protocols

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GCP/ICH Guidelines jobs

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Locations (7)

Locations (7)

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