Senior Clinical Research Associate

🕒 July 30

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

🇬🇧 UK Skilled Worker Visa Sponsor

This company has sponsored UK Skilled Worker visas in the past.

👻 Ghost score 27%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Pfizer

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1849

💼 Consulting

📣 Marketing

💊 Pharmaceuticals

💰 Post-IPO Debt on 2023-05

Consulting • Marketing • Pharmaceuticals

Pfizer is a pharmaceutical company that has been at the forefront of scientific innovation for 175 years. The company is dedicated to improving health and well-being at every stage of life by providing access to safe, effective, and affordable medicines and healthcare services. Pfizer focuses on delivering innovative therapies, particularly in the field of cancer treatments, as it continues to progress in transforming the healthcare landscape.

📋 Description

• Manage and monitor assigned investigator sites from site activation through database lock and closeout • Ensure clinical trials comply with monitoring plans, applicable laws, Good Clinical Practices, and Pfizer standards • Serve as primary contact for assigned investigator sites and manage investigator site relationships • Facilitate information flow among study team members, vendors, and investigator sites • Develop, coach, and train site personnel on protocols and compliance • Support enrollment and recruitment initiatives and resolve site activation and recruitment issues • Conduct onsite and remote/electronic monitoring for site initiation, routine monitoring, and site closure • Monitor adverse events and serious adverse events and collaborate with the Drug Safety Unit • Submit Trial Master File documentation, site reports, follow-up letters, protocol deviations, recruitment updates, supply management records, study progress, and metrics • Identify and resolve site issues and develop corrective and preventative actions • Resolve data queries and conduct investigator site close-out activities • Oversee investigational product receipt, handling, accounting, storage, and destruction • Support database release and serve as an unblinded monitor when appropriate • Maintain detailed understanding of products, protocols, and therapy areas • Support patient safety, eligibility, and clinical guidance to investigators • Drive quality event remediation and audit observation CAPA development when applicable • Mentor Clinical Research Associates when required

🎯 Requirements

• Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent • Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations • Minimum 3 years relevant experience in clinical research site monitoring • Some experience in Oncology • Global clinical trial experience • Fluency in English and the native language(s) of the country they will work in • Demonstrated knowledge of clinical research and development processes • Demonstrated knowledge of global and local regulatory requirements • Demonstrated understanding of monitoring, data acquisition and cleaning, reporting, and related operational elements • Knowledge of disease and technical areas pertaining to clinical studies, company direction, investigational products, and associated development plans • Ability to support sponsor regulatory interactions and inspections • Knowledge of protocol design and feasibility assessment processes • Understanding of regional/country culture and medical practice and their effects on clinical trial delivery • Ability to work in a matrix team environment and influence, drive/lead, and work through others • Ability to evaluate, interpret, and present complex issues and data for risk management and mitigation • Effective verbal and written communication skills • Ability to travel significantly within the area and occasionally internationally and on weekends

🏖️ Benefits

• Flexible workplace culture that encourages work-life harmony • Reasonable adjustments to support application and future career • Equal employment opportunity and diverse, inclusive workforce