Clinical Trials Manager

London Source: WhatJobs

See advert for pay

Overview

In this role you will lead and coordinate operational activities for assigned clinical studies, both domestically and globally. You will manage CROs and CSPs, ensuring studies comply with FDA, EU, ICH, and SOPs, while partnering with cross-functional teams. You’ll contribute to study design discussions, timelines, and monitoring plans to meet corporate goals. You will drive enrollment strategies and oversee both CRO-backed and in-house studies to maintain quality and timelines. This is an opportunity to shape clinical execution in a mission‑driven neuroscience-focused company.

Responsibilities

Ensure studies comply with FDA, EU, ICH, and SOPs/policies
Serve as primary operations contact for assigned studies
Contribute to study design discussions and study reports
Manage CROs/CSPs and monitor vendor performance
Lead study team meetings and manage timelines
Identify enrollment barriers and develop recruitment solutions
Oversee internally run studies including CRAs and monitoring plans
Collaborate to enforce standard processes across programs
Perform other duties as assigned

Key requirements

BS/BA degree with 6+ years of clinical trial management experience (domestic and international) or Master’s with 4+ years of experience
Detailed knowledge of clinical drug development, ICH, GCP, FDA regulations, and EU Directive
Strong clinical operations knowledge from start-up to close-out
Broad trial management and process knowledge
Ability to organize resources, set objectives, and provide direction
Leadership experience and ability to manage multiple teams
Excellent computer, communication, problem-solving, and analytical skills
Ability to meet multiple deadlines with high accuracy and efficiency
Experience partnering cross-functionally and with customers to drive results
Experience monitoring budgets and CRO/vendor management