Associate Clinical Project Manager (Clinical Research)

Формат работы

onsite

Тип работы

fulltime

Грейд

senior

Английский

Страна

Вакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:

TL;DR

Associate Clinical Project Manager (Clinical Research): Planning, executing, and reporting clinical studies from site initiation through close-out with an accent on recruitment, risk mitigation, regulatory compliance, and study team coordination. Focus on overseeing country-level trial execution, monitoring data quality and budgets, resolving operational issues, and supporting inspection readiness.

Location: Reading, Berkshire, United Kingdom

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

Plan, execute, monitor, and report assigned clinical studies from site initiation through study close-out.
Lead country, cluster, or hub study teams and coordinate communication with Trial Leads, CRAs, CRA Managers, and global clinical trial teams.
Track recruitment, enrollment, forecasts, study timelines, risks, mitigation plans, and corrective actions.
Oversee data management activities, monitoring visit reports, issue resolution, essential documents, site contracts, budgets, and invoiceable activities.
Coordinate CRA training, investigator meetings, study handovers, inspection readiness, audits, and implementation of corrective actions.
Promote compliance with sponsor standards, ICH GCP, applicable regulations, ethical requirements, and human subject protection principles.

Requirements

Bachelor’s degree in life sciences or a related field.
At least 5 years of relevant experience, including more than 1 year of project management experience, or an equivalent combination of education and experience.
Knowledge of clinical trial conduct, ICH GCP, applicable local laws, regulations, guidelines, and clinical protocols.
Good command of English is required. Strong written, verbal, presentation, problem-solving, organizational, prioritization, and collaboration skills are expected.
Experience with project financials, contractual obligations, Microsoft Word, Excel, and PowerPoint.
This role is not eligible for UK visa sponsorship.

Culture & Benefits

Work in a global clinical research and healthcare intelligence organization.
Collaborate across countries and geographies with awareness of cultural differences.
Operate within a culture focused on integrity, client focus, collaboration, innovation, ownership, quality, and ethical conduct.

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