Senior Clinical Research Associate

🔥 2 hours ago

🇮🇱 Israel – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 10%

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.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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 investigator site relationships and assigned clinical trial sites • Monitor clinical trials 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 • Coach and train site personnel and provide protocol training • Support enrollment and resolve site activation and recruitment issues • Conduct onsite and remote/electronic monitoring for initiation, routine monitoring and closure • Monitor adverse events and serious adverse events and collaborate with the Drug Safety Unit • Submit Trial Master File documentation, site reports, protocol deviations, recruitment updates, supply management and study metrics • Identify and resolve site issues and develop corrective and preventative actions • Resolve data queries and conduct site close-out activities • Oversee investigational product receipt, handling, accounting, storage and destruction • Support database release and undertake unblinded monitor responsibilities when required • Maintain product, protocol and therapy-area knowledge • Support patient safety, eligibility and clinical guidance • Drive Quality Event remediation and support audit observation CAPA activities

🎯 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 • Preferably 2 years in Oncology • Global clinical trial experience • Fluent in English and in the native language(s) of the country they will work in • Valid driver’s license and passport required • Significant travel (60-80%) within area • May require some international travel and weekend travel

🏖️ Benefits

• Flexible workplace culture supporting work-life harmony • Reasonable adjustments for disability inclusion • Equal employment opportunities • Significant travel opportunities within the assigned area • Pfizer patient-centric and breakthrough culture