Clinical Research Associate

🕒 July 11

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🇬🇧 UK Skilled Worker Visa Sponsor

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

👻 Ghost score 38%

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 • Ensure proper clinical trial conduct according to the Study Monitoring Plan, applicable laws, Good Clinical Practices, and Pfizer standards • Manage clinical trial activities from site initiation through database lock • Serve as primary contact for assigned investigator sites • Facilitate information flow among study team members, vendors, and investigator sites • Perform site development, coaching, and training • Attend investigator meetings when required, virtually or face-to-face • Support enrollment and resolve site activation and recruitment issues • Conduct remote assessment of e-diary data • Conduct onsite and remote/electronic monitoring for site initiation, routine monitoring, and closure • Monitor site-level AEs and SAEs and collaborate with the Drug Safety Unit • Submit required reports, documentation, updates, and tracking, including Trial Master File documentation and site reports • 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 as needed • Undertake unblinded monitor responsibilities where appropriate • Maintain product, protocol, and therapy-area knowledge • Support patient safety, eligibility, and clinical guidance • Drive Quality Event submission and remediation • Support audit conduct and CAPA development and checks

🎯 Requirements

• Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent • Knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations • Some relevant experience in clinical research site monitoring and management • Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases • Global clinical trial experience preferred • Must be fluent in English • Significant travel (60-80%) within area is required • May require some international travel and some weekend travel • Valid driver’s license and passport required

🏖️ Benefits

• Flexible workplace culture • Work-life harmony • Reasonable adjustments to support application and future career • Disability Confident Employer commitment • Equal employment opportunity and diverse, inclusive workforce