Clinical Medical Monitor & Safety Lead

Alimentiv Inc.; Glasgow; On-site; GBP 50,000 - 70,000; Full time

Job summary

A leading clinical research organization in Scotland is seeking a qualified medical professional to provide medical oversight and guidance during clinical trials. You will collaborate with clinical sites and study teams, ensuring compliance and safety throughout the study process. The ideal candidate has a medical degree, strong communication skills, and 4-6 years of experience in clinical trials. Responsibilities include reviewing protocols, assisting with data analysis, and communicating findings. Fluent English is a must.

Qualifications

• 4-6 years of related experience with ongoing training.
• Preferred experience in clinical trials, especially in a CRO environment.
• Ability to address protocol ambiguities and unforeseen medical scenarios.

Responsibilities

• Provide unbiased medical guidance to clinical sites.
• Assist with reviewing interim and final data sets.
• Document contacts and consult with medical directors.

Skills

Strong written and verbal communication

Clinical judgment

Analytical and critical thinking

Knowledge of drug development process

Fluency in English

Education

Medical degree

Job description

A leading clinical research organization in Scotland is seeking a qualified medical professional to provide medical oversight and guidance during clinical trials. You will collaborate with clinical sites and study teams, ensuring compliance and safety throughout the study process. The ideal candidate has a medical degree, strong communication skills, and 4-6 years of experience in clinical trials. Responsibilities include reviewing protocols, assisting with data analysis, and communicating findings. Fluent English is a must.